Аннотация:
The homogeneous azidophenylselenylation of diversely protected mono-, di- and trisaccharide glucals was studied to evaluate the influence of protective groups, N3 and I donors, temperature and solvent on the stereoselectivity of the formation of corresponding phenyl 2-azido-2-deoxy-1-seleno-α-D-gluco- and -manno-adducts.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
Yu. V. Mironov, A. A. Sherman, N. E. Nifantiev, “Homogeneous azidophenylselenylation of glucals”, Mendeleev Commun., 18:5 (2008), 241–243
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc3311
https://www.mathnet.ru/rus/mendc/v18/i5/p241
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Ekaterina D. Kazakova, Dmitry V. Yashunsky, Elena A. Khatuntseva, Nikolay E. Nifantiev, “Azidophenylselenylation of glycals towards 2-azido-2-deoxy-selenoglycosides and their application in oligosaccharide synthesis”, Pure and Applied Chemistry, 92:7 (2020), 1047
Mónica Guberman, Bartholomäus Pieber, Peter H. Seeberger, “Safe and Scalable Continuous Flow Azidophenylselenylation of Galactal to Prepare Galactosamine Building Blocks”, Org. Process Res. Dev., 23:12 (2019), 2764
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Elena A. Khatuntseva, Andrey A. Sherman, Yury E. Tsvetkov, Nikolay E. Nifantiev, “Phenyl 2-azido-2-deoxy-1-selenogalactosides: a single type of glycosyl donor for the highly stereoselective synthesis of α- and β-2-azido-2-deoxy-d-galactopyranosides”, Tetrahedron Letters, 57:6 (2016), 708
Sophie Nocquet‐Thibault, Anita Rayar, Pascal Retailleau, Kevin Cariou, Robert H. Dodd, “Iodine(III)‐Mediated Diazidation and Azido‐oxyamination of Enamides”, Chemistry A European J, 21:40 (2015), 14205
Hang Yin, Teng Wang, Ning Jiao, “Copper-Catalyzed Oxoazidation and Alkoxyazidation of Indoles”, Org. Lett., 16:9 (2014), 2302
Mattan Hurevich, Peter H. Seeberger, “Automated glycopeptide assembly by combined solid-phase peptide and oligosaccharide synthesis”, Chem. Commun., 50:15 (2014), 1851
Yunpeng Fan, Wen Wan, Guobin Ma, Wei Gao, Haizhen Jiang, Shizheng Zhu, Jian Hao, “Room-temperature Cu(ii)-catalyzed aromatic C–H azidation for the synthesis of ortho-azido anilines with excellent regioselectivity”, Chem. Commun., 50:43 (2014), 5733
Yu. V. Mironov, A. A. Grachev, A. V. Lalov, A. A. Sherman, M. P. Egorov, N. E. Nifantiev, “A study of the mechanism of the azidophenylselenylation of glycals”, Russ Chem Bull, 58:2 (2009), 284
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