Asymmetric induction in the nucleophilic addition in the series of aromatic azines / Egorov IN,Zyryanov GV,Rusinov VL,Chupakhin ON // USPEKHI KHIMII. - 2005. - V. 74, l. 12. - P. 1176-1192.

ISSN/EISSN:

0042-1308 / нет данных

Type:

Review

Abstract:

Stereoselective reactions of nucleophilic addition to the C = N bond in aromatic azines, resulting in chiral products, are surveyed. Various methods for inducing the optical activity are considered.

Author keywords:

ENANTIOPURE N-ACYLDIHYDROPYRIDONES; CHIRAL 1-ACYL-4-METHOXYPYRIDINIUM SALTS; REISSERT-TYPE REACTION; GRIGNARD-REAGENTS; 1-ACYLPYRIDINIUM SALTS; ENANTIOSELECTIVE ADDITION; DIASTEREOSELECTIVE ADDITION; QUINOLIZIDINE ALKALOIDS; ORGANOLITHIUM REAGENTS; BIFUNCTIONAL CATALYST

DOI:

нет данных

Web of Science ID:

ISI:000234937800002

Соавторы в МНС:

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Другие поля

Поле	Значение
Publisher	MEZHDUNARODNAYA KNIGA
Address	39 DIMITROVA UL., 113095 MOSCOW, RUSSIA
Language	Russian
Keywords-Plus	ENANTIOPURE N-ACYLDIHYDROPYRIDONES; CHIRAL 1-ACYL-4-METHOXYPYRIDINIUM SALTS; REISSERT-TYPE REACTION; GRIGNARD-REAGENTS; 1-ACYLPYRIDINIUM SALTS; ENANTIOSELECTIVE ADDITION; DIASTEREOSELECTIVE ADDITION; QUINOLIZIDINE ALKALOIDS; ORGANOLITHIUM REAGENTS; BIFUNCTIONAL CATALYST
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Multidisciplinary
Number-of-Cited-References	60
Usage-Count-Last-180-days	1
Usage-Count-Since-2013	2
Journal-ISO	Uspekhi Khimii
Doc-Delivery-Number	006ZY