Literatura académica sobre el tema "INDOLENT PRECURSOR"
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Artículos de revistas sobre el tema "INDOLENT PRECURSOR"
Pinto-Lopes, Pedro, Francisco Adao Fonseca, Roberto Silva, Pedro von Hafe y Elsa Fonseca. "Indolent systemic mastocytosis limited to the bone: a case report and review of the literature". Sao Paulo Medical Journal 131, n.º 3 (2013): 198–204. http://dx.doi.org/10.1590/1516-3180.2013.1313460.
Texto completoCanberk, Sule. "Precursor and borderline lesions of the thyroid (indolent lesions of epithelial origin): from theory to practice". Gland Surgery 9, n.º 5 (octubre de 2020): 1724–34. http://dx.doi.org/10.21037/gs-20-429.
Texto completoLussier, Tyler, Natalie Schoebe y Sabine Mai. "Risk Stratification and Treatment in Smoldering Multiple Myeloma". Cells 11, n.º 1 (31 de diciembre de 2021): 130. http://dx.doi.org/10.3390/cells11010130.
Texto completoMarchegiani, Giovanni, Stefano Andrianello, Tommaso Pollini, Andrea Caravati, Giuseppe Malleo, Marco Biancotto, Claudio Bassi y Roberto Salvia. "Natural History of Intraductal Papillary Mucinous Neoplasm of the Pancreas Reappraisal of the Indolent Precursor of Pancreatic Cancer". Journal of the American College of Surgeons 227, n.º 4 (octubre de 2018): e37-e38. http://dx.doi.org/10.1016/j.jamcollsurg.2018.08.099.
Texto completoPurdy, Adam, Firas Ido y Deborah Stahlnecker. "Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia (DIPNECH): A Case of Indolent Pulmonary Nodules Diagnosed with Robotic-Assisted Navigational Bronchoscopy". Case Reports in Pulmonology 2021 (10 de diciembre de 2021): 1–4. http://dx.doi.org/10.1155/2021/6312296.
Texto completoGarcia-Montero, Andres C., Maria Jara-Acevedo, Ivan Alvarez-Twose, Cristina Teodosio, Laura Sanchez-Muñoz, Javier Ignacio Muñoz-Gonzalez, Andrea Mayado et al. "KIT D816V Mutation Positive Bone Marrow Mesenchymal Stem Cells in Indolent Systemic Mastocytosis Are Associated with Disease Progression". Blood 126, n.º 23 (3 de diciembre de 2015): 4058. http://dx.doi.org/10.1182/blood.v126.23.4058.4058.
Texto completoMarchegiani, Giovanni, Stefano Andrianello, Tommaso Pollini, Andrea Caravati, Marco Biancotto, Giuseppe Malleo, Claudio Bassi y Roberto Salvia. "The natural history of intraductal papillary mucinous neoplasms of the pancreas: Reappraisal of the indolent precursor of pancreatic cancer". Pancreatology 18, n.º 4 (junio de 2018): S2—S3. http://dx.doi.org/10.1016/j.pan.2018.05.011.
Texto completoMarchegiani, G., S. Andrianello, T. Pollini, A. Caravati, M. Biancotto, G. Malleo, C. Bassi y R. Salvia. "The natural history of intraductal papillary mucinous neoplasm of the pancreas: Reappraisal of the indolent precursor of pancreatic cancer". HPB 20 (septiembre de 2018): S195. http://dx.doi.org/10.1016/j.hpb.2018.06.051.
Texto completoLópez, Cristina, Pablo Mozas, Armando López-Guillermo y Sílvia Beà. "Molecular Pathogenesis of Follicular Lymphoma: From Genetics to Clinical Practice". Hemato 3, n.º 4 (26 de septiembre de 2022): 595–614. http://dx.doi.org/10.3390/hemato3040041.
Texto completoKhanlari, Mahsa y Jennifer R. Chapman. "Follicular lymphoma: updates for pathologists". Journal of Pathology and Translational Medicine 56, n.º 1 (15 de enero de 2022): 1–15. http://dx.doi.org/10.4132/jptm.2021.09.29.
Texto completoTesis sobre el tema "INDOLENT PRECURSOR"
Mcausland, Donald Euan Reynolds. "Arynes in synthesis : new reaction and precursor development". Thesis, University of Manchester, 2014. https://www.research.manchester.ac.uk/portal/en/theses/arynes-in-synthesisnew-reaction-and-precursor-development(1f59c4ec-dc6d-487b-9bc4-c5a99d5bc030).html.
Texto completoCiccolini, Cecilia. "Synthesis of Mono and Poly-Heterocycles starting from 1,2-Diaza-1,3-Dienes (or precursors) as Building Blocks". Doctoral thesis, Urbino, 2020. http://hdl.handle.net/11576/2674162.
Texto completoWen, Xin. "The Utilization of Sulfonylhydrazones as New Radical Precursors for Asymmetric Radical C–H Alkylation via Co(II)-Based Metalloradical Catalysis". Thesis, Boston College, 2019. http://hdl.handle.net/2345/bc-ir:108292.
Texto completoAsymmetric C–H functionalization represents one of the central topics in modern organic chemistry, which allows for the direct installation of functional groups onto ubiquitous C–H bonds in organic molecules. Among numerous elegant strategies, transition metal-catalyzed C–H alkylation with diazo compounds represents one of the most powerful methods for C–C bond formation. Different from Fischer metallocarbene-based C–H insertion reactions, cobalt(II)-based metalloradical catalysis (MRC) is recently proven to be capable of activating acceptor/acceptor diazo compounds for radical C–H alkylation reactions via H-atom abstraction. In this dissertation, we have developed several systems by utilizing less-explored aryl and alkyl diazomethanes as new radical precursors for highly enantioselective radical C–H alkylation reactions, which permit the efficient synthesis of different optically active heterocyclic compounds. First, we have demonstrated the feasibility of using aryl aldehyde-derived sulfonylhydrazones as new radical precursors for enantioselective radical C–H alkylation to synthesis enantioenriched 2,3-dihydrobenzofuran derivatives. Notably, a general and mild way for in situ generation of diazo compounds have been identified by using 2,4,6-triisopropyl sulfonyl hydrazone as diazo precursor, which allow us to regulate the reaction temperature to achieve the high enantioselectivity for the desired radical reactions. Second, the utility of Co(II)-based MRC has been further highlighted by enantioselective indoline synthesis. Through the design and synthesis of new catalysts, the system is shown to have a broad spectrum of substrate scope, forming various 2-substituted indolines with up to 98% yield and 96% ee. A series of mechanistic studies further support the underlying stepwise radical alkylation pathway. Finally, we further expand the applicability of MRC to even more challenging diazo compounds, aliphatic diazomethanes. Starting from alkyl aldehyde-derived sulfonylhydrazones as diazo precursors, the Co(II)-based radical alkylation reactions allow for the enantioselective synthesis for common 2-substituted tetrahydrofuran structures with high yields and excellent enantioselectivities
Thesis (PhD) — Boston College, 2019
Submitted to: Boston College. Graduate School of Arts and Sciences
Discipline: Chemistry
Marchegiani, Giovanni. "THE NATURAL HISTORY OF INTRADUCTAL PAPILLARY MUCINOUS NEOPLASM OF THE PANCREAS: REAPPRAISAL OF THE INDOLENT PRECURSOR OF PANCREATIC CANCER". Doctoral thesis, 2018. http://hdl.handle.net/11562/978425.
Texto completoChen, Yu-Jen y 陳俞臻. "The Synthesis and Photochemistry of Radical Pair Precursors: N-Benzenesulfonyl Substituted Pyrroles, Imidazole and Indole". Thesis, 2002. http://ndltd.ncl.edu.tw/handle/3287f4.
Texto completo國立交通大學
應用化學系
90
A series of 39, 47, 52 and 53 in 2-methyltetrahydrofuran glass matrices at 77 K were irradiated with 230-325 nm (NiSO4-filtered, UV light), which gave triplet EPR spectra, and the zero-field splitting (zfs) parameters D' values are 0.0228, 0.0225, 0.0190 and 0.0176 cm-1, respectively. At 4 K, the D' values of 51 and 47 are 0.0239 and 0.0237 cm-1, respectively. The radical pairs derived from 51 (12-44 K) and 47 (8-52 K) both showed linear Curie plots, thereby indicating either the ground state are triplets or that singlet and triplet states are degenerate (≦30 cal/mole difference). An addition product of Ts and MNP was observed when 51 was photolyzed in the presence of spin trapping agent. N-benzenesulfonyl substituted hetercyclic molecules 85 and 88 also gave triplet EPR spectra, which are consistent with triplet radical pairs. Results indicate that nitro-sulfur bonds were easily cleaved by 230-325 nm photolysis, and the results are supported by ab initio calculations. Therefore, the reported D' value (0.0226 cm-1) of a biradical by Professor Berson in the photolysis of N-tosyl pyrrole diazene 18 (J. A. Berson, J. Am. Chem. Soc. 1997, 119, 1416.) may not be a triplet biradical and could be a triplet radical pair instead.
Capítulos de libros sobre el tema "INDOLENT PRECURSOR"
Politi, V., M. V. Lavaggi, G. Di Stazio y A. Margonelli. "Indole-3-Pyruvic Acid as a Direct Precursor of Kynurenic Acid". En Advances in Experimental Medicine and Biology, 515–18. Boston, MA: Springer New York, 1991. http://dx.doi.org/10.1007/978-1-4684-5952-4_57.
Texto completoGrogan, Martha. "Cardiac amyloidosis". En ESC CardioMed, 1545–49. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198784906.003.0373.
Texto completo"Alkaloids I". En Natural Product Biosynthesis, 264–315. The Royal Society of Chemistry, 2022. http://dx.doi.org/10.1039/bk9781839165641-00264.
Texto completo"Isoprenoids/Terpenes". En Natural Product Biosynthesis, 192–263. The Royal Society of Chemistry, 2022. http://dx.doi.org/10.1039/bk9781839165641-00192.
Texto completoTaber, Douglass. "Alkaloid Synthesis: (-)-Aurantioclavine (Stoltz), (-)-Esermethole (Nakao/Hiyama/ Ogoshi), (-)-Kainic Acid (Tomooka), Dasycarpidone (Bennasar), (-)-Cephalotaxine (Ishibashi) and Lysergic Acid (Fujii/Ohno)". En Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0060.
Texto completoActas de conferencias sobre el tema "INDOLENT PRECURSOR"
Трофимов, Б., B. Trofimov, Н. Гусарова y N. Gusarova. "The development of original methodologies of directed synthesis of le-Carbs their analogs and precursors base donacetylene and its derivatives". En Topical issues of translational medicine: a collection of articles dedicated to the 5th anniversary of the day The creation of a department for biomedical research and technology of the Irkutsk Scientific Center Siberian Branch of RAS. Москва: INFRA-M Academic Publishing LLC., 2017. http://dx.doi.org/10.12737/conferencearticle_58be81ec92d17.
Texto completoBlasko, Gy, G. Blasko, G. Sas y Cs Szantay. "MODULATION OF THROMBIN-MEDIATED REACTIONS IN HAEMOSTASIS- BY TREQUINSIN AND ITS ANALOGUES." En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643432.
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