Reactions of triazines and tetrazines with dienophiles (Review) / Prokhorov A. M.,Kozhevnikov D. N. // CHEMISTRY OF HETEROCYCLIC COMPOUNDS. - 2012. - V. 48, l. 8. - P. 1153-1176.

ISSN/EISSN:

0009-3122 / нет данных

Type:

Article

Abstract:

Information on the development of a valuable synthetic methodology based on inverse electron-demand Diels-Alder reaction in the series of pi-deficient azadienes (triazines and tetrazines) is summarized and classified. By this method it is possible to obtain mono-, di-, and triazines containing functional substituents both from the initial azine and from the dienophile. Such reactions are often the simplest and even the only possible method for the synthesis of substances with properties suitable for practical applications.

Author keywords:

azadienes; pyridazines; pyridines; pyrimidines; tetrazines; triazines; Diels-Alder reaction INVERSE-ELECTRON-DEMAND; DIELS-ALDER REACTIONS; SIMPLE LEGO SYSTEM; HIGHLY SUBSTITUTED PYRIDINES; ONE-POT SYNTHESIS; 2,2'-BIPYRIDINE DERIVATIVES; CONVENIENT SYNTHESIS; 4+2 CYCLOADDITIONS; DIMETHYL 1,2,4,5-TETRAZINE-3,6-DICARBOXYLATE; NUCLEOPHILIC-SUBSTITUTION

DOI:

10.1007/s10593-012-1117-9

Web of Science ID:

ISI:000311671400002

Соавторы в МНС:

Другие поля

Поле	Значение
Month	NOV
Publisher	SPRINGER
Address	233 SPRING ST, NEW YORK, NY 10013 USA
Language	English
Keywords-Plus	INVERSE-ELECTRON-DEMAND; DIELS-ALDER REACTIONS; SIMPLE LEGO SYSTEM; HIGHLY SUBSTITUTED PYRIDINES; ONE-POT SYNTHESIS; 2,2'-BIPYRIDINE DERIVATIVES; CONVENIENT SYNTHESIS; 4+2 CYCLOADDITIONS; DIMETHYL 1,2,4,5-TETRAZINE-3,6-DICARBOXYLATE; NUCLEOPHILIC-SUBSTITUTION
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Organic
Author-Email	aprohor@yandex.ru dnk@ios.uran.ru
ResearcherID-Numbers	Prokhorov, Anton/B-9789-2011
Number-of-Cited-References	134
Usage-Count-Last-180-days	1
Usage-Count-Since-2013	51
Journal-ISO	Chem. Heterocycl. Compds.
Doc-Delivery-Number	045CC