Relevant bibliographies by topics / Rearrangement

Academic literature on the topic 'Rearrangement'

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Published: 4 June 2021
Last updated: 25 May 2024

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Journal articles on the topic "Rearrangement"

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Greaney, Michael F., and David M. Whalley. "Recent Advances in the Smiles Rearrangement: New Opportunities for Arylation." Synthesis 54, no. 08 (December 1, 2021): 1908–18. http://dx.doi.org/10.1055/a-1710-6289.

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AbstractThe Smiles rearrangement has undergone a renaissance in recent years providing new avenues for non-canonical arylation techniques in both the radical and polar regimes. This short review will discuss recent applications of the reaction (from 2017 to late 2021), including its relevance to areas such as heterocycle synthesis and the functionalization of alkenes and alkynes as well as glimpses at new directions for the field.1 Introduction2 Polar Smiles Rearrangements3 Radical Smiles: Alkene and Alkyne Functionalization4 Radical Smiles: Rearrangements via C–X Bond Cleavage5 Radical Smiles: Miscellaneous Rearrangements6 Conclusions
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Polprasert, Chantana, Chantiya Chanswangphuwana, Weerapat Owattanapanich, Smith Kungwankiattichai, Ekarat Rattarittamrong, Thanawat Rattanathammethee, Wasithep Limvorapitak, et al. "Clinical Characteristics and Outcomes of Myeloid Neoplasms with Mecom Rearrangement: Results from a Nationwide Multicenter Study." Blood 142, Supplement 1 (November 28, 2023): 4213. http://dx.doi.org/10.1182/blood-2023-180100.

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MECOM rearrangements are detected in myeloid neoplasms [myelodysplastic neoplasm (MDS) and acute myeloid leukemia (AML)] which are associated with dismal prognosis. Classic MECOM rearrangements include inv(3)(q21q26.2) and t(3;3)(q21;q26) while non-classic subtypes are 3q26.2/ MECOM rearrangement with other partners. Both classic and non-classic rearrangements result in MECOM overexpression which involves in the process of leukemogenesis. Recently, the World Health Organization classification 2022 categorized myeloid neoplasms with these genetic abnormalities as “AML with MECOM rearrangement” regardless of blast count. We aim to explore frequency, clinical characteristics and outcomes including treatment response in this AML subtype among Thai myeloid neoplasms. AML data was collected from a national registry which were conducted by Thai acute leukemia working group. Other than AML with MECOM rearrangements, AML was categorized as favorable, intermediate, and adverse risk groups according to European Leukemia Network 2022. MDS data was collected from a multicenter study group involving 4 medical centers. Other than MDS with MECOM rearrangements, MDS was categorized into 5 risk groups according to R-IPSS score system (very low, low, intermediate, high and very high-risk groups). Myeloid neoplasms with MECOM rearrangements were analyzed among their diseases and grouped together and compared to MDS and AML cohorts. A total of 9 cases of myeloid neoplasms with MECOM rearrangement were detected. Among non-M3 AML cases, there were 6 cases with MECOM rearrangement from 746 non-M3 AML (0.8%) while 3 cases were detected in 163 MDS (1.8%). Seven of 9 cases (78%) were female gender. Five of 9 cases were classic MECOM rearrangement [1 case with inv(3)(q21q26.2) and 4 cases with t(3;3)(q21;q26)] while the other 4 cases were non-classic rearrangements [3 cases with t(3;21)(q26.2;q22) and 1 case with t(3;7)(q26;q21)]. In the AML cohort, AML with MECOM rearrangement showed lower white blood cell, but higher platelet counts compared to other groups (favorable, intermediate, and adverse risk groups) ( Table 1). Among AML cases receiving intensive chemotherapy, MECOM rearrangement subgroup showed lower complete response (CR) rate compared to others favorable, intermediate, and adverse risk groups. (0% vs. 77.3% vs. 37.6% vs. 23.8%; p<0.001). Of note, among 6 AML with MECOM rearrangement, there were 4 patients who received intensive chemotherapy but none of them responded to the treatment. In the MDS cohort, MDS with MECOM rearrangement showed lower hemoglobin and platelet counts compared to other groups ( Table 2). Among 3 MDS with MECOM rearrangement, one patient received azacitidine with investigational drug (sabatolimab/placebo) and achieved complete hematologic response. He eventually progressed after 12 cycles of the treatments and subsequently died. When combining 3 MDS and 6 AML with MECOM rearrangement as one group and compared survival rate with others: survival rate of 9 myeloid neoplasms with MECOM rearrangementis worse than the adverse group of AML and the very high risk group MDS with a 1-year survival rate of 22% ( Figure 1 and 2). In conclusion, myeloid neoplasms with MECOM rearrangements are rare with the frequency of 0.8% in non-M3 AML and 1.8% in MDS. This subtype is more common in female gender. The prognosis of myeloid neoplasms with MECOM rearrangement is dismal with a 1-year survival rate of 16.7% in AML and 6-month survival rate of 33% in MDS. Chemotherapy should be avoided in this subtype due to non-responsiveness, hypomethylating agent showed benefit and can be considered as a bridging treatment before stem cell transplantation. Novel therapy targeting MECOM gene should be further explored to improve outcomes in this AML subtype.
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Margolis, D., M. Yassai, A. Hletko, L. McOlash, and J. Gorski. "Concurrent or sequential delta and beta TCR gene rearrangement during thymocyte development: individual thymi follow distinct pathways." Journal of Immunology 159, no. 2 (July 15, 1997): 529–33. http://dx.doi.org/10.4049/jimmunol.159.2.529.

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Abstract Analysis of TCR rearrangement profiles of well-defined thymocyte populations in a number of individual thymi provides evidence for a new pathway of lineage commitment. In all of the thymi analyzed, alphabeta thymocytes have rearrangements in the delta locus that are enhanced for out-of-frame rearrangements. Thus, not only did alphabeta thymocytes pass through a stage in differentiation that included delta rearrangement, but they also constitute a population that was relatively unsuccessful at these rearrangements. Interestingly, in some thymi, gammadelta thymocytes have out-of-frame beta rearrangements. This represents a novel pathway in which delta and beta rearrangement happens concurrently. In this pathway, selection favors whichever gene is in frame, thus improving the chances of generating useful T cells. In other thymi, gammadelta cells showed no obvious beta gene rearrangement, indicating a sequential rearrangement. Thus, alphabeta/gammadelta lineage commitment can follow at least two distinct pathways in different individuals.
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Zhang, Beibei, Xiaoxian Li, Boying Guo, and Yunfei Du. "Hypervalent iodine reagent-mediated reactions involving rearrangement processes." Chemical Communications 56, no. 91 (2020): 14119–36. http://dx.doi.org/10.1039/d0cc05354f.

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We summarize the developments of hypervalent iodine reagents-mediated reactions involving [1,2]-migration, Hofmann rearrangement, Beckmann rearrangement, ring contraction/expansion, [3,3]-sigmatropic/iodonium-Claisen rearrangement and some miscellaneous rearrangements.
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Annamareddy, Ajay, Bu Wang, Paul M. Voyles, and Dane Morgan. "Distribution of atomic rearrangement vectors in a metallic glass." Journal of Applied Physics 132, no. 19 (November 21, 2022): 195103. http://dx.doi.org/10.1063/5.0125531.

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Short-timescale atomic rearrangements are fundamental to the kinetics of glasses and frequently dominated by one atom moving significantly (a rearrangement), while others relax only modestly. The rates and directions of such rearrangements (or hops) are dominated by the distributions of activation barriers ( Eact) for rearrangement for a single atom and how those distributions vary across the atoms in the system. We have used molecular dynamics simulations of Cu50Zr50 metallic glass below Tg in an isoconfigurational ensemble to catalog the ensemble of rearrangements from thousands of sites. The majority of atoms are strongly caged by their neighbors, but a tiny fraction has a very high propensity for rearrangement, which leads to a power-law variation in the cage-breaking probability for the atoms in the model. In addition, atoms generally have multiple accessible rearrangement vectors, each with its own Eact. However, atoms with lower Eact (or higher rearrangement rates) generally explored fewer possible rearrangement vectors, as the low Eact path is explored far more than others. We discuss how our results influence future modeling efforts to predict the rearrangement vector of a hopping atom.
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Tawa, A., SH Benedict, J. Hara, N. Hozumi, and EW Gelfand. "Rearrangement of the T cell receptor gamma-chain gene in childhood acute lymphoblastic leukemia." Blood 70, no. 6 (December 1, 1987): 1933–39. http://dx.doi.org/10.1182/blood.v70.6.1933.1933.

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Abstract We analyzed rearrangements of the T cell receptor gamma-chain (T gamma) gene as well as rearrangements of the T cell receptor beta-chain (T beta) gene and immunoglobulin heavy-chain (IgH) gene in 68 children with acute lymphoblastic leukemia (ALL). All 15 patients with T cell ALL showed rearrangements of both T beta and T gamma genes. Twenty-four of 53 non-T, non-B ALL patients (45%) showed T gamma gene rearrangements and only 14 of these also showed T beta gene rearrangements. Only a single patient rearranged the T beta gene in the absence of T gamma gene rearrangement. The rearrangement patterns of the T gamma gene in non-T, non-B ALL were quite different from those observed in T cell ALL, as 20 of 23 patients retained at least one germline band of the T gamma gene. In contrast, all T cell ALL patients showed no retention of germline bands. These data indicate that rearrangement of the T gamma gene is not specific for T cell ALL. Further, the results also suggest that T gamma gene rearrangement precedes T beta gene rearrangement. The combined analysis of rearrangement patterns of IgH, T beta, and T gamma genes provides new criteria for defining the cellular origin of leukemic cells and for further delineation of leukemia cell heterogeneity.
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Tawa, A., SH Benedict, J. Hara, N. Hozumi, and EW Gelfand. "Rearrangement of the T cell receptor gamma-chain gene in childhood acute lymphoblastic leukemia." Blood 70, no. 6 (December 1, 1987): 1933–39. http://dx.doi.org/10.1182/blood.v70.6.1933.bloodjournal7061933.

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We analyzed rearrangements of the T cell receptor gamma-chain (T gamma) gene as well as rearrangements of the T cell receptor beta-chain (T beta) gene and immunoglobulin heavy-chain (IgH) gene in 68 children with acute lymphoblastic leukemia (ALL). All 15 patients with T cell ALL showed rearrangements of both T beta and T gamma genes. Twenty-four of 53 non-T, non-B ALL patients (45%) showed T gamma gene rearrangements and only 14 of these also showed T beta gene rearrangements. Only a single patient rearranged the T beta gene in the absence of T gamma gene rearrangement. The rearrangement patterns of the T gamma gene in non-T, non-B ALL were quite different from those observed in T cell ALL, as 20 of 23 patients retained at least one germline band of the T gamma gene. In contrast, all T cell ALL patients showed no retention of germline bands. These data indicate that rearrangement of the T gamma gene is not specific for T cell ALL. Further, the results also suggest that T gamma gene rearrangement precedes T beta gene rearrangement. The combined analysis of rearrangement patterns of IgH, T beta, and T gamma genes provides new criteria for defining the cellular origin of leukemic cells and for further delineation of leukemia cell heterogeneity.
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Aster, J. C., and J. Sklar. "Interallelic V(D)J trans-rearrangement within the beta T cell receptor gene is infrequent and occurs preferentially during attempted D beta to J beta joining." Journal of Experimental Medicine 175, no. 6 (June 1, 1992): 1773–82. http://dx.doi.org/10.1084/jem.175.6.1773.

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Previous work has demonstrated that intergenic V(D)J rearrangement, a process referred to as trans-rearrangement, occurs at an unexpectedly high frequency. These rearrangements generate novel V(D)J combinations which could conceivably have some role in the normal immune system, and since they probably arise through chromosomal rearrangements akin to those associated with lymphoid neoplasia, they may also serve as a model for investigating recombinational events which underlie oncogenesis. In view of the existence of a mechanism that permits relatively frequent intergenic trans-rearrangements, it seems reasonable that interallelic trans-rearrangements involving segments belonging to each of the two alleles of a single antigen receptor gene might also occur. To determine the frequency of such rearrangements, we examined thymocytes of F1 progeny of a cross between SWR mice, which have a deletion spanning 10 of the known V beta segments, and NZW mice, which have a deletion involving all J beta 2 segments. Rearranged TCR-beta genes containing V beta segments from the NZW chromosome and J beta segments from the SWR chromosome were amplified from the DNA of F1 thymocytes with the polymerase chain reaction. Using this approach, we found that such rearrangements are relatively uncommon, being present in about 1 in 10(5) thymocytes, a frequency lower than that of V gamma/J beta intergenic trans-rearrangements. The ratio of conventional cis-rearrangement to interallelic trans-rearrangement for any particular V beta segment appears to be about 10(4):1. The structure of the junctions in all trans-rearrangements analyzed closely resembles conventional cis-rearrangements, indicating involvement of V(D)J recombinase in the ultimate joining event. However, in contrast to cis-rearrangements, a strong bias for inclusion of D beta 1 segments over D beta 2 segments was noted, suggesting that interallelic trans-rearrangement may occur preferentially during attempted D-J joining. J beta 2 segment usage in trans-rearrangements also appeared to differ from that expected from previously studied cis-rearrangements. The results have implications with respect to the events and timing of conventional cis-rearrangement during thymocyte differentiation, and the prevalence of various types of trans-rearrangements.
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Asou, N., M. Matsuoka, T. Hattori, F. Kawano, S. Maeda, K. Shimada, and K. Takatsuki. "T cell gamma gene rearrangements in hematologic neoplasms." Blood 69, no. 3 (March 1, 1987): 968–70. http://dx.doi.org/10.1182/blood.v69.3.968.968.

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Abstract Rearrangements of the T cell gamma (T gamma) gene were studied in primary neoplastic cells from 75 patients with leukemia or lymphoma. T gamma gene rearrangements were observed in 19 of 21 T cell neoplasms; 14 of 21 immature B cell leukemias, including 4 out of 5 patients with rearrangements of both immunoglobulin heavy-chain (JH) and T cell receptor beta chain (T beta) genes; none out of 16 nonlymphoid leukemias. Thus, T gamma gene rearrangement is frequently found in immature B cells and is not always found in T cells showing T beta gene rearrangement, but it is not detected in nonlymphoid cells. Furthermore, T gamma gene rearrangement in cells with the germline configuration of the JH and T beta genes was observed. These results indicate that the detection of T gamma gene rearrangement does not allow a clear assignment to a particular lineage. However, an analysis of T gamma gene rearrangement provides a further potential tool to establish the lymphoid cellular origin and clonality of hematologic neoplasms and identify the normal stages of lymphocyte differentiation.
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Asou, N., M. Matsuoka, T. Hattori, F. Kawano, S. Maeda, K. Shimada, and K. Takatsuki. "T cell gamma gene rearrangements in hematologic neoplasms." Blood 69, no. 3 (March 1, 1987): 968–70. http://dx.doi.org/10.1182/blood.v69.3.968.bloodjournal693968.

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Rearrangements of the T cell gamma (T gamma) gene were studied in primary neoplastic cells from 75 patients with leukemia or lymphoma. T gamma gene rearrangements were observed in 19 of 21 T cell neoplasms; 14 of 21 immature B cell leukemias, including 4 out of 5 patients with rearrangements of both immunoglobulin heavy-chain (JH) and T cell receptor beta chain (T beta) genes; none out of 16 nonlymphoid leukemias. Thus, T gamma gene rearrangement is frequently found in immature B cells and is not always found in T cells showing T beta gene rearrangement, but it is not detected in nonlymphoid cells. Furthermore, T gamma gene rearrangement in cells with the germline configuration of the JH and T beta genes was observed. These results indicate that the detection of T gamma gene rearrangement does not allow a clear assignment to a particular lineage. However, an analysis of T gamma gene rearrangement provides a further potential tool to establish the lymphoid cellular origin and clonality of hematologic neoplasms and identify the normal stages of lymphocyte differentiation.
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Dissertations / Theses on the topic "Rearrangement"

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Mohamed, Mustafa Abdi. "Synthesis of [alpha]-allynyl and [alpha]-allylsilane amino acids by the Claisen rearrangement /." *McMaster only, 2001.

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Christie, David Alan. "Genome rearrangement problems." Thesis, University of Glasgow, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.284780.

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Yoon, Tehshik Peter MacMillan David W. C. "The acyl-Claisen rearrangement development of a novel metal-catalyzed Claisen rearrangement and enantioselective variants of the acyl-Claisen rearrangement /." Diss., Pasadena, Calif. : California Institute of Technology, 2002. http://resolver.caltech.edu/CaltechTHESIS:01282010-153053761.

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Thesis (Ph. D.)--California Institute of Technology, 2002. PQ #3052855.
Advisor names found in the Acknowledgments pages of the thesis. Title from home page. Viewed 02/11/2010. Includes bibliographical references.
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Mountford, David Mark. "Novel Claisen rearrangement reactions." Thesis, Imperial College London, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.415168.

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Copeland, Fiona B. M. "Low energy rearrangement collisions." Thesis, Queen's University Belfast, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.318881.

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Lang, Stuart. "Rearrangement of organic azides." Thesis, University of Strathclyde, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.415093.

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Alabdullah, Basil. "Stereoselective organoborate rearrangement reactions." Thesis, Cardiff University, 2015. http://orca.cf.ac.uk/75961/.

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This thesis describes the use of organoborate rearrangement reactions to generate quaternary carbon centres, with the ultimate goal of exploring new procedures for the asymmetric synthesis of chiral quaternary carbon centres. Chapter One: this chapter contains a historical review of the use of organoboranes in organic synthesis, focusing mainly on the use of boronic esters in asymmetric organic synthesis. Chapter Two: this chapter focuses on attempts at developing a catalytic method for the generation of quaternary stereocentres using migration reactions of boronic esters with n-butyllithium in the presence of chiral catalysts. This study showed that the reaction is stoichiometric in the absence of the Lewis acid. However, there were strong indications of catalytic turn over in some experiments. Chapters Three and Four: these chapters focus on attempts at designing a chiral version of the DCME reaction using sulfur compounds. Chapter Three focuses on attempts at evaluating a heterocyclic system, specifically a dithiane, as a stereocontrol agent in its reaction with trialkylboranes. The study showed that using 2-methoxy-1,3-dithiane-oxide achieved formation of the double and triple migration product but in poor yield. Chapter Four contains a detailed investigation into the synthesis and evaluation of non-cyclic sulfur compounds such as sulfoxides, sulfoximines, sulfilimines and sulfones for generation of chiral tertiary alcohols. The study of the reaction of dichloromethyl phenyl sulfoxide with trialkylboranes showed a new type of aldol-like reaction. This reaction was utilised to synthesise a series of new compounds. Also, the study of the reaction of dichloromethyl-p-tolyl sulfone with trialkylboranes showed a new type of reaction by replacing the hydrogen with the alkyl group from the trialkylborane. Finally, the study of the reaction of N-methyl-S-(dichloromethyl)-S-phenylsulfoximine with trialkylboranes showed production of the desired triple migration product in moderate to very good yield.
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Hester, Alison J. "The anionic thia-fries rearrangement." Thesis, University of Bristol, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.430204.

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Sollogoub, Matthieu. "Le triisobutylaluminium (tibal) et les sucres : rearrangements et debenzylation le ti(iv) un autre agent de rearrangement." Paris 6, 1999. http://www.theses.fr/1999PA066480.

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Le triisobutylaluminium (tibal) est le reactif de choix pour effectuer la transposition du carbone et de l'oxygene dans un ether d'enol dont l'ether possede un groupement electro-donneur en. Dans le domaine des sucres ce rearrangement permet la transformation, unique, d'un glycoside en carbocycle avec conservation de l'aglycone. Cette reaction est aussi effectuee par cl 3tioipr. Nous avons exploite cette reaction en l'appliquant a des disaccharides dans le but de synthetiser de facon directe des carba-disaccharides. Nous avons aussi reussi a transformer des composes dont l'aglycone n'est pas oxygenee (s-, se-, c-glycosides). Finalement nous avons mis en evidence une autre action remarquable du tibal sur les sucres : la de-o-benzylation regioselective des composes -methyl perbenzyles.
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Yang, Yanbo. "Pd0-Catalyzed Formal 1,3-Diaza-Claisen Rearrangement. Design And Development Of Cationic 1,3-Diaza-Claisen Rearrangement." ScholarWorks @ UVM, 2014. http://scholarworks.uvm.edu/graddis/261.

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The dissertation describes Pd0-catalyzed formal 1,3-diaza-Claisen rearrangement and the design and development of cationic 1,3-diaza-Claisen rearrangement. Our previous work has shown that isocyanates react with azanorbornenes and azabicyclo[2.2.2]octenes under thermal conditions to afford zwitterionic intermediates that undergo a thermal 1,3-diaza-Claisen rearrangement to give both ureas and isoureas. However, some azanorbornenes and azabicyclooctenes failed to rearrange or proceeded in low yields. To address these challenging substrates for the thermal 1,3-diaza-Claisen rearrangement, we have developed a Pd0-catalyzed formal 1,3-diaza-Claisen rearrangement. Interestingly, under Pd0-catalyzed condition, both isocyanates with electron-withdrawing groups and isocyanates without electron-withdrawing groups react with azanorbornenes and azabicyclo[2.2.2]octenes to provide ureas as the only products in high yields. More importantly, the reactions that failed under thermal conditions were all successful under Pd0-catalysis. In addition to azanorbornenes and azabicyclo[2.2.2]octenes, other ring systems were also investigated. Pd0 catalysis has broadened the scope of tertiary allylic amines that react with isocyanates to afford 1,3-diaza-Claisen rearrangement products. In the presence of p-TsCl and NEt3, allylaminopropyl benzyl ureas were initially dehydrated to form protonated carbodiimides whose presence was confirmed by the infrared absorption frequency at 2100 cm-1 which is the characteristic band of -N=C=N-; then the in situ generated protonated carbodiimides were poised for further cationic 1,3-diaza-Claisen rearrangement to afford synthetically challenging guanidines. The effect of acid on the rearrangement was ascertained by the fact that no rearrangement product was observed by simply heating free base carbodiimide 3.10 in benzene at reflux. Other dehydration reagents, such as Tf2O, Ts2O, MsCl were also investigated, and none of them provide satisfactory results. A selection of allyamino benzyl ureas with different tether length, substituents, or in varied ring systems, were synthesized to explore the scope of this methodology. This methodology works best at allylaminopropyl benzyl ureas, and the substituents on the benzyl group does not seem to affect the reaction rate in a significant way.
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Books on the topic "Rearrangement"

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D, Hames B., and Glover David M, eds. Gene rearrangement. Oxford [England]: IRL Press, 1990.

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Skovron, Alex. The rearrangement. Carlton, Vic: Melbourne University Press, 1988.

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The rearrangement: A novel. New York: Macmillan, 1985.

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Rearrangement of the invisible. [Madera, Calif.]: Poetic Matrix Press, 2012.

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Lin, Zhi-Ping. Some applications of ultrasound irradiation in pinacol coupling of carbonyl compounds. Hauppauge, N.Y: Nova Science Publishers, 2010.

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Armstrong, Philip N. Data rearrangement and real-time computation. Santa Monica, CA: Rand Corp., 1993.

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Martin, Hiersemann, and Nubbemeyer Udo, eds. The Claisen rearrangement: Methods and applications. Weinheim: Wiley-VCH, 2007.

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Butel, Elizabeth. Margaret Preston: The art of constant rearrangement. New York, N.Y: Viking in association with the Art Gallery of New South Wales, 1986.

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Jaeger, Sharon Elka. Nitrogen analogues of the [2,3]-Wittig rearrangement. Manchester: University of Manchester, 1996.

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Smyth, Donald. Acid induced rearrangement to form cyclohexadienyliron complexes. Norwich: University of East Anglia, 1994.

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Book chapters on the topic "Rearrangement"

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Li, Jie Jack. "Nametkin rearrangement (Retropinacol rearrangement)." In Name Reactions, 279. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_207.

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Li, Jie Jack. "Nametkin rearrangement (Retropinacol rearrangement)." In Name Reactions, 250. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_196.

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Li, Jie Jack. "Zinin benzidine rearrangement (semidine rearrangement)." In Name Reactions, 453–54. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_331.

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Li, Jie Jack. "Zinin benzidine rearrangement (semidine rearrangement)." In Name Reactions, 407–8. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_315.

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Li, Jie Jack. "Favorskii rearrangement and Quasi-Favorskii rearrangement." In Name Reactions, 132–33. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_102.

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Li, Jie Jack. "Favorskii rearrangement and Quasi-Favorskii rearrangement." In Name Reactions, 116–17. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_95.

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Li, Jie Jack. "Ferrier rearrangement." In Name Reactions, 135. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_104.

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Li, Jie Jack. "Fries rearrangement." In Name Reactions, 149–50. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_114.

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Li, Jie Jack. "Hayashi rearrangement." In Name Reactions, 177–78. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_134.

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Li, Jie Jack. "Bamberger rearrangement." In Name Reactions, 18. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_14.

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Conference papers on the topic "Rearrangement"

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Weihs, Luca, Matt Deitke, Aniruddha Kembhavi, and Roozbeh Mottaghi. "Visual Room Rearrangement." In 2021 IEEE/CVF Conference on Computer Vision and Pattern Recognition (CVPR). IEEE, 2021. http://dx.doi.org/10.1109/cvpr46437.2021.00586.

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Rahman, M. D., Ralph R. Dammel, and Dana L. Durham. "Rearrangement of novolak resins." In SPIE's 1994 Symposium on Microlithography, edited by Omkaram Nalamasu. SPIE, 1994. http://dx.doi.org/10.1117/12.175382.

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Moon, Sung Ho, Hyung Ho Park, Andrea Goldsmith, and Minseok Oh. "Bit Rearrangement for MIMO Retransmissions." In IEEE GLOBECOM 2007-2007 IEEE Global Telecommunications Conference. IEEE, 2007. http://dx.doi.org/10.1109/glocom.2007.666.

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Wu, Yujing, Zheyan Piao, Jun-Ho Kim, and Jin-Gyun Chung. "CAN compression using signal rearrangement." In 2014 IEEE Asia Pacific Conference on Circuits and Systems (APCCAS). IEEE, 2014. http://dx.doi.org/10.1109/apccas.2014.7032866.

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Gokhale, Maya, Scott Lloyd, and Chris Hajas. "Near memory data structure rearrangement." In MEMSYS '15: International Symposium on Memory Systems. New York, NY, USA: ACM, 2015. http://dx.doi.org/10.1145/2818950.2818986.

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Wu, Shiquan, and Xun Gu. "Multiple Genome Rearrangement By Reversals." In Proceedings of the Pacific Symposium. WORLD SCIENTIFIC, 2001. http://dx.doi.org/10.1142/9789812799623_0024.

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Huang, Eric, Zhenzhong Jia, and Matthew T. Mason. "Large-Scale Multi-Object Rearrangement." In 2019 International Conference on Robotics and Automation (ICRA). IEEE, 2019. http://dx.doi.org/10.1109/icra.2019.8793946.

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Tonmaithong, Karun, Supawan Annanab, and Nopporn Chotikakamthorn. "Handwriting rearrangement for Thai calligraphy." In 2016 8th International Conference on Information Technology and Electrical Engineering (ICITEE). IEEE, 2016. http://dx.doi.org/10.1109/iciteed.2016.7863249.

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Plachouras, Christos, and Marius Miron. "Music Rearrangement Using Hierarchical Segmentation." In ICASSP 2023 - 2023 IEEE International Conference on Acoustics, Speech and Signal Processing (ICASSP). IEEE, 2023. http://dx.doi.org/10.1109/icassp49357.2023.10097212.

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Madsen, Mickey P., Milovan Kovacevic, Jakob D. Monster, Jeppe A. Pedersen, Arnold Knott, and Michael A. E. Andersen. "Input-output rearrangement of isolated converters." In 2015 IEEE Power and Energy Conference at Illinois (PECI). IEEE, 2015. http://dx.doi.org/10.1109/peci.2015.7064917.

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Reports on the topic "Rearrangement"

1

Wang, Paul. Alumina-catalyzed Cope rearrangement. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.2402.

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Jacob, Josemon. Atom transfer and rearrangement reactions catalyzed by methyltrioxorhenium, MTO. Office of Scientific and Technical Information (OSTI), May 1999. http://dx.doi.org/10.2172/354892.

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Berg, Harlan. Kinetics of the Cope rearrangement of 3,4-diphenylhexa-1,5-diene. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.1116.

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Galichon, Alfred, Ivan Fernandez-Val, and Victor Chernozhukov. Improving point and interval estimates of monotone functions by rearrangement. Institute for Fiscal Studies, July 2008. http://dx.doi.org/10.1920/wp.cem.2008.1708.

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Woloschak, G. E., C. R. Libertin, P. Weaver, M. Churchill, and C. M. Chang-Liu. Rearrangement of RAG-1 recombinase gene in radiation-sensitive ``wasted`` mice. Office of Scientific and Technical Information (OSTI), September 1993. http://dx.doi.org/10.2172/10184999.

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Woloschak, G. E., C. R. Libertin, P. Weaver, M. Churchill, and Chin-Mei Chang-Liu. Rearrangement of RAG-1 recombinase gene in radiation-sensitive ``wasted`` mice. Office of Scientific and Technical Information (OSTI), August 1994. http://dx.doi.org/10.2172/10175212.

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Woloschak, G. E., C. R. Libertin, P. Weaver, M. Churchill, and C. M. Chang-Liu. Rearrangement of RAG-1 recombinase gene in DNA-repair deficient ``wasted`` mice. Office of Scientific and Technical Information (OSTI), November 1993. http://dx.doi.org/10.2172/10105564.

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Kim, Chong Bok. Gas-phase generations and rearrangement of silathiones, R sub 2 Si=S. Office of Scientific and Technical Information (OSTI), January 1991. http://dx.doi.org/10.2172/5996188.

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Haber, J. E. FASEB summer research conference on genetic recombination and chromosome rearrangement. Final report. Office of Scientific and Technical Information (OSTI), March 1998. http://dx.doi.org/10.2172/763942.

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Orkin, Stuart H. Exploring the Mechanisms of Pathogenesis in Prostate Cancer Involving TMPRSS2-ERG (Or ETV1) Gene Rearrangement. Fort Belvoir, VA: Defense Technical Information Center, January 2008. http://dx.doi.org/10.21236/ada491425.

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You might also be interested in the extended bibliographies on the topic 'Rearrangement' for particular source types:
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