tert-amino effect in heterocyclic chemistry. Synthesis of hydrogenated spiro derivatives of quinolines / D'yachenko EV,Glukhareva TV,Nikolaenko EF,Tkachev AV,Morzherin YY // RUSSIAN CHEMICAL BULLETIN. - 2004. - V. 53, l. 6. - P. 1240-1247.

ISSN/EISSN:

1066-5285 / нет данных

Type:

Article

Abstract:

A new method was developed for the one-step synthesis of spiro derivatives of fused quinolines by the reactions of ortho-amino derivatives of benzaldehyde with Meldrum's acid, cyclohexane-1,3-dione, or N,N'-disubstituted barbituric acids.

Author keywords:

tert-amino effect; cyclization; nitrogen-containing heterocycles; spiro derivatives; quinoline RING-CLOSURE REACTIONS; SIMPLE ROUTE

DOI:

10.1023/B:RUCB.0000042280.7172

Web of Science ID:

ISI:000224147800015

Соавторы в МНС:

Другие поля

Поле	Значение
Month	JUN
Publisher	CONSULTANTS BUREAU
Address	233 SPRING ST, NEW YORK, NY 10013 USA
Language	English
Keywords-Plus	RING-CLOSURE REACTIONS; SIMPLE ROUTE
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Multidisciplinary
Author-Email	atkachev@nioch.nsc.ru morjerine@htf.ustu.ru
ResearcherID-Numbers	Morzherin, Yury/M-7420-2013 Glukhareva, Tatiana/A-4610-2016
ORCID-Numbers	Morzherin, Yury/0000-0002-1333-6676 Glukhareva, Tatiana/0000-0002-5231-9879
Number-of-Cited-References	16
Usage-Count-Since-2013	3
Journal-ISO	Russ. Chem. Bull.
Doc-Delivery-Number	857VR