Relevant bibliographies by topics / Synthesis of thioamide

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Synthesis of thioamide'

Author: Grafiati
Published: 18 May 2024

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Journal articles on the topic "Synthesis of thioamide"

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Dong, Zhi-Bing, Meng-Tian Zeng, Min Wang, Han-Ying Peng, and Yu Cheng. "Copper-Catalyzed Synthesis of Aryl Thioamides from Aryl Aldehydes and Tetramethylthiuram Disulfide." Synthesis 50, no. 03 (2017): 644–50. http://dx.doi.org/10.1055/s-0036-1590936.

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A novel and convenient method for the synthesis of aryl thioamides from aryl aldehydes and tetramethylthiuram disulfide (TMTD) without the use of sulfurating reagent was explored. In the presence of CuI and di-tert-butyl peroxide (DTBP), various aryl thioamides were prepared with good to excellent yields, tetramethylthiuram disulfide as thioamide source is essential for this transformation. The protocol features broad substrate scope, nice yields, operability and commercially available and inexpensive raw materials, showing its practical synthetic value in organic synthesis.
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Sauvé, Gilles, Vanga S. Rao, Gilles Lajoie, and Bernard Belleau. "Backbone-modified oligopeptidic bioregulators. The synthesis and configuration of thioamide, amidoxime, cyanoamidine, and amidrazone analogs of the chemotactic peptide N-formyl-methionyl-leucyl-phenylalanine (f-Met-Leu-Phe-OR)." Canadian Journal of Chemistry 63, no. 11 (1985): 3089–101. http://dx.doi.org/10.1139/v85-511.

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Reaction conditions for the synthesis of thioamide, amidoxime, and N-substituted amidine analogs of the peptide bond are described. Several new amidine analogs of the chemotactic peptide f-Met-Leu-Phe-OR were synthesized using the thioamides as precursors. The assignment of the E/Z configuration was accomplished by nuclear magnetic resonance. The biological activity of these analogs is briefly described.
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Fong, Mei, Wit K. Janowski, Rolf H. Prager, and Max R. Taylor. "A Convenient Synthesis of 2-Substituted Thiazole-5-carboxylates." Australian Journal of Chemistry 57, no. 6 (2004): 599. http://dx.doi.org/10.1071/ch03252.

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The photolysis of ethyl 5-oxo-2-phenyl-2,5-dihydroisoxazole-4-carboxylate in acetonitrile containing 0.5% tri- fluoroacetic acid in the presence of thioamides gives moderate (40–60%) yields of thiazole-5-carboxylate esters. In the absence of trifluoroacetic acid, the intermediate vinyl thioesters can be isolated. That addition of the thioamide to the first formed carbene was, through sulfur, confirmed by X-ray crystal structures of 2-methylthiazole-5-carboxylic acid and a byproduct.
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Szantai-Kis, D., Christopher Walters, Taylor Barrett, Eileen Hoang, and E. Petersson. "Thieme Chemistry Journals Awardees – Where Are They Now? Improved Fmoc Deprotection Methods for the Synthesis of Thioamide-Containing Peptides and Proteins." Synlett 28, no. 14 (2017): 1789–94. http://dx.doi.org/10.1055/s-0036-1589027.

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Site-selective incorporation of thioamides into peptides and proteins provides a useful tool for a wide range of applications. Current incorporation methods suffer from low yields as well as epimerization. Here, we describe how the use of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) rather than piperidine in fluorenylmethyloxycarbonyl (Fmoc) deprotection reduces epimerization and increases yields of thioamide-containing peptides. Furthermore, we demonstrate that the use of DBU avoids byproduct formation when synthesizing peptides containing side-chain thioamides.
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Zhang, Qiang, Laurent Soulère, and Yves Queneau. "Towards More Practical Methods for the Chemical Synthesis of Thioamides Using Sulfuration Agents: A Decade Update." Molecules 28, no. 8 (2023): 3527. http://dx.doi.org/10.3390/molecules28083527.

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Compounds possessing a thioamide function play a crucial role in organic synthesis, serving as key building blocks. They are also important in the pharmaceutical chemistry and drug design, owing to their ability to mimic the amide function in biomolecules while retaining or developing biological activity. From the synthetic viewpoint, several methods have been developed for preparing thioamides using sulfuration agents. The purpose of this review is to give an update of the last decade of contributions focusing on the formation of thioamides employing different sulfur sources. When appropriate
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Pham Xuan Thao. "Study on the synthesis of thioamides from aldehyde N-tert-butylsulfinyl amide and sulfur in aqueous media." Journal of Military Science and Technology, no. 76 (December 12, 2021): 54–60. http://dx.doi.org/10.54939/1859-1043.j.mst.76.2021.54-60.

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Thioamides have been widely used in the fields of medicine and organic chemistry, some of which are essential bioactive compounds, plant protection agents, and drugs. It could also be used as a vulcanizing agent, an additive to lubricants and greases, and a ligand in organic synthesis. Usually, thioamide is synthesized at high temperatures or in the microwave using an expensive noble metal complex as catalysts. This paper presented a straightforward method for synthesizing thioamides by using N-tert-butylsulfinyl amide, aldehyde, and sulfur. The reaction was carried out in water, which is an e
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Hammam, A. S., and B. E. Bayoumy. "Reaction of thioamides with 2,3-dichloro-1,4-naphthoquinone. A novel synthesis of naphtho[2,3-d]thiazole-4,9-diones." Collection of Czechoslovak Chemical Communications 50, no. 1 (1985): 71–79. http://dx.doi.org/10.1135/cccc19850071.

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The reaction of thioamide II with 2,3-dichloro-1,4-naphthoquinone (I) in ethanol gave naptho[2,3-d]thiazole-4,9-diones (IV). The intermediates, 2-thioamido-3-chloro-1,4-naphthoquinones III were also isolated from the reaction medium and could be separately transformed to IV by further boiling in aqueous ethanol containing bicarbonate. The reaction of thiosemicarbazide with I under similar conditions gave naphtho[2,3-e]-2-amino-4H-1,3,4-thiadiazine-5,10-dione (VII).
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Sharma, Shubham, Dharmender Singh, Sunit Kumar, et al. "An efficient metal-free and catalyst-free C–S/C–O bond-formation strategy: synthesis of pyrazole-conjugated thioamides and amides." Beilstein Journal of Organic Chemistry 19 (March 2, 2023): 231–44. http://dx.doi.org/10.3762/bjoc.19.22.

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An operationally simple and metal-free approach is described for the synthesis of pyrazole-tethered thioamide and amide conjugates. The thioamides were generated by employing a three-component reaction of diverse pyrazole C-3/4/5 carbaldehydes, secondary amines, and elemental sulfur in a single synthetic operation. The advantages of this developed protocol refer to the broad substrate scope, metal-free and easy to perform reaction conditions. Moreover, the pyrazole C-3/5-linked amide conjugates were also synthesized via an oxidative amination of pyrazole carbaldehydes and 2-aminopyridines usin
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Yeo, Chien, and Edward Tiekink. "O-Methyl m-Tolylcarbamothioate." Molbank 2018, no. 3 (2018): M1020. http://dx.doi.org/10.3390/m1020.

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The synthesis, spectroscopic, and crystallographic characterisation of the title compound, O-methyl m-tolylcarbamothioate, MeOC(=S)N(H)(m-tolyl) (1), are described. The crystallographic study confirms the structure determined by spectroscopy and shows the presence of the thioamide tautomer, a syn-disposition of the thione-S and thioamide-N-H atoms and, in the crystal, thioamide-N-H…S(thione) hydrogen bonding leading to an eight-membered {…HNCS}2 synthon.
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Cakmak, M., I. I. Ozturk, C. N. Banti, et al. "Bismuth(III) bromide-thioamide complexes: synthesis, characterization and cytotoxic properties." Main Group Metal Chemistry 41, no. 5-6 (2018): 143–54. http://dx.doi.org/10.1515/mgmc-2018-0035.

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Abstract New bismuth(III) bromine compounds of the heterocyclic thioamides were prepared and structurally characterized. The reaction of heterocyclic thioamides with bismuth(III) bromide resulted in the formation of the {[BiBr2(μ2-Br)(MMI)2]2·CH3COCH3·H2O} (1), {[BiBr2(MBZIM)4]·Br·2H2O} (2), {[BiBr2(μ2-Br)(tHPMT)2]2·CH3CN} (3), {[BiBr2(μ2-Br)(PYT)2]2·CH3CN} (4) and {[BiBr2(μ2-Br)(MBZT)2]2 2CH3OH} (5) complexes (MMI: 2-mercapto-1-methylimidazole, MBZIM: 2-mercaptobenzimidazole, tHPMT: 2-mercapto-3,4,5,6-tetrahydro-pyrimidine, PYT: 2-mercaptopyridine and MBZT: 2-mercaptobenzothiazole). The compl
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Dissertations / Theses on the topic "Synthesis of thioamide"

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Brandes, Dee Anne. "The synthesis and reactivity of alpha,beta-unsaturated thioamide, thioester, and thione iron tricarbonyl complexes." Thesis, University of Ottawa (Canada), 1990. http://hdl.handle.net/10393/6008.

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$\alpha,\beta$-Unsaturated thioamide, thioester and thione iron tricarbonyl complexes 1-13 were prepared from the free ligands and iron pentacarbonyl using photolysis or diiron nonacarbonyl using thermolysis. X-ray crystal structures were obtained for the free ligand 2$\sp\prime,$ (PhCH=C(Ph)C(S)NEt$\sb2$), and for complexes 1 and 2, $\rm\lbrack \overline{\overline{Fe(PhCH}{=}CHC(S})NEt\sb2)$(CO)$\sb3\rbrack$ and $\rm\lbrack \overline{\overline{Fe(PhCH}{=}C(Ph)C(S})NEt\sb2)$(CO)$\sb3\rbrack$ respectively. Thioamide and thioester iron tricarbonyl complexes gave triphenylphosphine substituted co
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Mukherjee, Suvodip. "Methodological approach on carbon-hetero bond formation reaction." Thesis, University of North Bengal, 2022. http://ir.nbu.ac.in/handle/123456789/4792.

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Kienz, Torben [Verfasser]. "Exploration of N-ferrocenyl substituted thioamides : synthesis, properties and reactivity / Torben Kienz." Mainz : Universitätsbibliothek Mainz, 2016. http://d-nb.info/1120619912/34.

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Ellwood, A. R. "A synthetic approach to the sarain core and development of new thioamide-based methodologies." Thesis, University College London (University of London), 2011. http://discovery.ucl.ac.uk/1332893/.

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Sarain A is a marine alkaloid that was isolated from the Mediterranean sponge Reniera sarai; the alkaloid possesses antibacterial, insecticidal and antitumour properties. As a result of the intriguing structure of this alkaloid, it has quickly become a popular target for organic chemists. Arguably the most challenging part of its synthesis is the tricyclic core, which is surrounded by two macrocyclic rings. This thesis describes two separate approaches towards the core, both utilising a thia-Claisen rearrangement as a key step. The first approach involved the ring expansion of a 5,5-bicyclic a
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LELONG, BRUNO. "Synthese diastereoselective de thioamides ' et -dihydroxyles : une voie d'acces aux valerolactones." Caen, 1997. http://www.theses.fr/1997CAEN2059.

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L'objectif de ce travail est l'hydroboration chimio- et diastereoselective de composes thiocarbonyles -insatures. Ces molecules sont en effet de bons precurseurs pour synthetiser des valerolactones de facon assez simple. Apres avoir montre que la reaction d'hydroboration n'est pas chimioselective vis a vis des dithioesters, et constate que la reaction d'hydroboration sur les dithiocetals -ethyleniques n'est pas diastereoselective, nous nous sommes tournes vers la fonction thioamide pour acceder aux lactones. Les -hydroxythioamides -ethyleniques requis sont synthetises par thiorearrangement de
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ABOUSAID, LEKBIR. "Etude cinetique de la thioamidation en serie aromatique. Synthese et caracterisation des (co)polyamide-thioamides." Caen, 1996. http://www.theses.fr/1996CAEN2031.

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Les bis(dithioester)s iso et terephtaliques ont ete synthetises a partir de bis(chloromethyl)benzene ou des diacides phtaliques. La reaction d'un exces de diamines sur ces composes conduit a la formation de nombreux bis(thioamide-amine)s et bis(thioamide)s derives avec de bons rendements. Associes au chlorure de phtaloyle, les bis(thioamide-amine)s ont donne des (co)polyamide-thioamides amorphes contenant de nombreuses structures cycliques. Ces nouveaux copolymeres ont ete caracterises par spectroscopie #1h, #1#3c rmn, ir, uv-vsible, mesure de viscosite et analyse enthalpique differentielle (d
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Rodriguez-Garcia, Valerie. "Efficient methodology for the synthesis of 2,4-benzodiazepin-1-ones, sulfonylbenzotriazoles, sulfonamides, ethylene sulfonamides, thiocarbamates, dithiocarbamates and thioamides." [Gainesville, Fla.] : University of Florida, 2004. http://purl.fcla.edu/fcla/etd/UFE0006303.

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Kulesza, Joanna. "Synthesis and studies of binding properties of calix[4]arenes functionalised with amide and hydroxamate moities and their thiocarbonyl analogues." Strasbourg, 2011. http://www.theses.fr/2011STRA6093.

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Afin de pouvoir suivre les teneurs en cations de métaux lourds toxiques pour les organismes vivants tels que Pb2+ ou Cd2+, il est nécessaire de concevoir des composés hautement sélectifs. Ce travail porte sur la synthèse et l’étude de dérivés amides et hydroxyamides de calix[4]arènes et de leurs analogues thiocarbonylés. Vingt sept dérivés (thioamides, amides, hydroxamates et acides hydroxamiques) ont été obtenus. Différentes techniques ont permis l’étude des interactions entre ces ligands et des cations métalliques: spectroscopie RMN du 1H, diffraction des rayons X, extraction liquid-liquid,
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Mykhaylychenko, Sergiy. "Study of perfluoroketene dithioacetals and N,S-acetals for the synthesis of fluorinated acyclic and heterocyclic compounds." Rouen, 2008. http://www.theses.fr/2008ROUES066.

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Les dithioacétals de perfluorocétènes sont des « synthons » simples et polyvalents pour la synthèse d'une large variété de composés fluorés acycliques et cycliques. Des transformations efficaces et directes des g-lactones a,b-insaturées en g-lactames et en pyridazin-3-ones substitués par un groupement 2,2,2-trifluoroéthyle ont été effectuées, à partir d'amines primaires et d'hydrazines variées et des dithioacétals de perfluorocétènes. La structure de tous les nouveaux composés a été assignée en utilisant les données de RMN (19F, 1H, 13C), d'IR et de MS et par diffraction des rayons X. Les réac
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Khatri, Bhavesh. "Exploring Nature's Inventory: Investigating the Role of Amide to Thioamide Substitution on Protein Stability." Thesis, 2020. https://etd.iisc.ac.in/handle/2005/5635.

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The peptide backbone holds a protein together and plays a crucial role in guiding its three-dimentional structure. The tertiary structure of proteins regulates several biological processes. Therefore, peptide bond modification has gained significant attention to influence protein folding, stability, and functions. However, it is a challenging task to mimic the peptide (amide) bond due to its unique properties, such as planar structure, hydrogen bond donor, and acceptor properties. Thioamide, a single O to S substitution in an amide bond, is the closest isostere and has shown promising results
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Books on the topic "Synthesis of thioamide"

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Reilly, William Leo 1926. Some Reactions of Fluorocarbon Nitriles: Syntheses of Amidines, Thioamides and Triazines. Creative Media Partners, LLC, 2021.

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Book chapters on the topic "Synthesis of thioamide"

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Murai, Toshiaki. "Synthesis of Thioamides." In Chemistry of Thioamides. Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-7828-7_3.

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Kumagai, Naoya, and Masakatsu Shibasaki. "Asymmetric Synthesis Using Thioamides." In Chemistry of Thioamides. Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-7828-7_5.

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Yan, Hong, and Hai-Chao Xu. "Synthesis of Heterocycles from Thioamides." In Chemistry of Thioamides. Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-7828-7_6.

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Zhang, Xue, Jinhua Yang, and Junfeng Zhao. "Ynamide-Mediated Synthetic Approach to Thioamide-Substituted Peptides." In Methods in Molecular Biology. Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2489-0_6.

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Kantlehner, W. "Synthesis from α-Phosphoryl Thioamide Derivatives." In Three Carbon-Heteroatom Bonds: Ketenes and Derivatives. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-024-00418.

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Chou, Jonathan Chiu-Chun, Veronica E. Stafford, Grace E. Kenney, and Laura M. K. Dassama. "The enzymology of oxazolone and thioamide synthesis in methanobactin." In Synthetic and Enzymatic Modifications of the Peptide Backbone. Elsevier, 2021. http://dx.doi.org/10.1016/bs.mie.2021.04.008.

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Taber, Douglass F. "Enantioselective Preparation of Alkylated Stereogenic Centers." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0042.

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Jon D. Stewart of the University of Florida established (Chem. Commun. 2010, 46, 8558) a scalable enzymatic reduction of geranial 1 to citronellal 2. Andreas S. Bommarius of Georgia Tech reported (Chem. Commun. 2010, 46, 8809) related studies. Isamu Shiina of the Tokyo University of Science developed (J. Am. Chem. Soc. 2010, 132, 11629) a nucleophilic catalyst for the kinetic resolution of α-chiral carboxylic acids such as 3. David W. C. MacMillan of Princeton University devised (J. Am. Chem. Soc. 2010, 132, 13600) a protocol for the enantioselective benzylation of an aldehyde 5. Kian L. Tan of Boston College (J. Am. Chem. Soc. 2010, 132, 14757) and Shannon S. Stahl and Clark R. Landis of the University of Wisconsin (J. Am. Chem. Soc. 2010, 132, 14027) developed the regioselective enantioselective hydroformylation of alkenes such as 7 with chelating substituents. Masaya Sawamura of Hokkaido University (J. Am. Chem. Soc. 2010, 132, 879) and others (Org. Lett. 2010, 12, 2438; Tetrahedron Lett. 2010, 5592, 6018) effected enantiospecific allylic coupling, as in the conversion of 9 to 10 . James P. Morken, also of Boston College, achieved (J. Am. Chem. Soc. 2010, 132, 10686) enantioselective allylation of 11. Ben L. Feringa of the University of Groningen devised (J. Am. Chem. Soc. 2010, 132, 13152) a protocol for net enantioselective conjugate addition to an α, β-unsaturated alde hyde 14. Gary A. Molander of the University of Pennsylvania found (J. Am. Chem. Soc. 2010, 132, 17108) that coupling of 16, prepared by enantioselective conjugate addition, proceeded with inversion. Naoya Kumagai and Masakatsu Shibasaki of the Institute of Microbial Chemistry effected (J. Am. Chem. Soc. 2010, 132, 10275) enantioselective alkynylation of the thioamide 18, and Takahiro Nishimura and Tamio Hayashi of Kyoto University achieved (Chem. Commun. 2010, 46, 6837) conjugate alkynylation of the nitroalkene 20. Several other protocols (Angew. Chem. Int. Ed. 2010, 49, 5780, 7299, 8145; J. Am. Chem. Soc. 2010, 132, 14373; J. Org. Chem. 2010, 75, 7829) have been developed for the catalytic enantioselective construction of arylated stereogenic centers.
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Taber, Douglass F. "Stereocontrolled C-N Ring Construction: The Pyne Synthesis of Hyacinthacine B 3." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0054.

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Keiji Maruoka of Kyoto University found (Organic Lett. 2010, 12, 1668) that the diazo amide 1 derived from the Oppolzer sultam condensed with the imine 2 to give the aziridine 3 with high stereocontrol. Andrei K. Yudin of the University of Toronto observed (Angew. Chem. Int. Ed. 2010, 49, 1607) that the unprotected aziridine aldehyde 4, which exists as a mixture of dimers, condensed smoothly with the Ohira reagent 5 to give the alkynyl aziridine 6. David M. Hodgson of the University of Oxford successfully (Angew. Chem. Int. Ed. 2010, 49, 2900) deprotonated the azetidine thioamide 7 to give, after allylation, the azetidine 8. Varinder K. Aggarwal of the University of Bristol devised (Chem. Commun. 2010, 267) a Pd catalyst for the cyclocarbonylation of an alkenyl aziridine 9 to give the β-lactam 10. Iain Coldham of the University of Sheffield used (J. Org. Chem. 2010, 75, 4069) the ligand they had developed to effect enantioselective allylation of the pyrrolidine derivative 11. The corrresponding piperidine worked as well. John P. Wolfe of the University of Michigan established (Organic Lett. 2010, 12, 2322) that the Pd-mediated cyclization of 13 to 15 could be effected with high diastereocontrol. Christopher G. Frost of the University of Bath optimized (Angew. Chem. Int. Ed. 2010, 49, 1825) the tandem Ru-mediated conjugate addition/cyclization of 16 to give 18 in high ee. Barry M. Trost of Stanford University extended (J. Am. Chem. Soc. 2010, 132, 8238) their studies of trimethylenemethane cycloaddition to the ketimine 19, leading to the substituted pyrrolidine 21 in high ee. Pher G. Andersson of Uppsala University optimized (J. Am. Chem. Soc. 2010, 132, 8880) an Ir catalyst for the enantioselective hydrogenation of readily prepared tetrahydropyridines such as 22. Min Shi of the Shanghai Institute of Organic Chemistry devised (J. Org. Chem. 2010, 75, 3935) a Pd catalyst for enantioselective conjugate addition to the prochiral pyridone 24. Xiaojun Huang of Roche Palo Alto prepared (Tetrahedron Lett. 2010, 51, 1554) the monoacid 26 by enantioselective methanolysis of the anhydride. Selective formylation of the ester led to the pyridone 27.
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Tang, R. Y. "22.1.7.2 Thioamides (Update 2024)." In Knowledge Updates 2024/1. Georg Thieme Verlag KG, 2023. http://dx.doi.org/10.1055/sos-sd-122-00021.

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Abstract This is an update to the earlier Science of Synthesis contribution describing methods for the synthesis of thioamides, with a focus on the literature published in the period 2005-2022. In this time, a number of new synthetic methods for the preparation of thioamides have been developed. A variety of substrates, including amides, aldehydes, ketones, nitriles, carboxylic acids, thiocarboxylic acids, β-oxo carboxylic acids, alkynes, alkenes, oximes, benzylamines, benzylic alcohols, benzylic thiols, benzyl disulfides, active methylene compounds, and isothiocyanates have been applied in these transformations. The sulfur agents used include Lawesson’s reagent, elemental sulfur, sulfide salts, phosphorus pentasulfide, thiourea, dithiophosphate, carbon disulfide, and thiophosphoryl chloride.
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Braverman, S., M. Cherkinsky, and M. L. Birsa. "Synthesis of Thioamides." In Four Carbon-Heteroatom Bonds. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-018-00203.

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Conference papers on the topic "Synthesis of thioamide"

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Stojković, Danijela, Maja Đukić, Marija Ristić, et al. "Synthesis, characterization and HSA interactions of a new piano-stool ruthenium(II) complex containing a thioamide-type ligand." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.507s.

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The synthesis and characterization of a newly synthesized piano-stool [Ru-(ɳ6-p-cymene)Cl2L] complex with a ligand 3-amino-2-cyano-N-phenyl-3-(4-phenyl-1-piperazinyl)-2-propenethioamide are presented. The complex was obtained in good yield as an ochre powderand was characterized by elemental analysis, 1H and 13C NMR, IR, conductometry, and melting point. The fluorescence binding studies showed that the interaction of the complex with albumin occurs by a static quenching mechanism and that the complex showed a very high value of the binding constant with one binding site (Kb = 1.68 × 107; n = 1
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Dekamin, Mohammad G., Niaz Kheirabi, and Zahra Karimi. "A green and facile ultrasound-promoted synthesis of thioamide derivatives catalyzed by Cu(I)@Chitosan as a new bio-polymeric nano catalyst in aqueous media." In The 19th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2015. http://dx.doi.org/10.3390/ecsoc-19-a028.

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Dotsenko, Victor, Konstantin Frolov, and Sergey Krivokolysko. "DMSO-HCl System as an Efficient Oxidant of Thioamides and Selenoamides." In The 16th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2012. http://dx.doi.org/10.3390/ecsoc-16-01073.

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Levchenko, Arina G., Polina G. Dahno, and Victor V. Dotsenko. "Synthesis of N-(hydroxymethylene)thioamides by N-hydroxymethylation of 2-cyanothioacrylamides." In ECSOC-25. MDPI, 2021. http://dx.doi.org/10.3390/ecsoc-25-11799.

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Heimgartner, Heinz, Jürg Lehmann, and Anthony Linden. "Site-Selective Incorporation of Thioamide-Linkages into a Growing Peptide via Variation of the 'Azirine/Oxazolone Method'." In The 1st International Electronic Conference on Synthetic Organic Chemistry. MDPI, 1997. http://dx.doi.org/10.3390/ecsoc-1-02033.

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Muntyan, Victoria S., Mariia E. Vladimirova, Alexey M. Afonin, Alexey N. Muntyan, and Marina L. Roumiantseva. "ANALYSIS OF SALT-SENSITIVE AND SALT-TOLERANT SINORHIZOBIUM MELILOTI STRAINS USING DNA MICROARRAY, PHENOTYPE MICROARRAY AND GENOME MINING TECHNIQUES." In 23rd SGEM International Multidisciplinary Scientific GeoConference 2023. STEF92 Technology, 2023. http://dx.doi.org/10.5593/sgem2023/6.1/s25.15.

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Abstract:
Nodule bacteria increase the resistance of host plants to abiotic stress factors; however, the role of the genetic potential of rhizobia in the formation of productive salt-tolerant plant-microbial symbiosis remains underestimated. The aim of the study was to evaluate the pool of genes responsible for the salt tolerance of the alfalfa microsymbiont, Sinorhizobium meliloti, using the DNA microarray technique, phenotype microarray (PM), NGS and NNGS-technologies and genome mining (antismash 5.0). As a result of the analysis of the genomes of strains contrastingly different in salt tolerance, it
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