Diastereoselective synthesis of spiro derivatives of 3-substituted 2,3,4,4a,5,6-hexahydro-1H-benzo{[}c]quinolizines / Glukhareva T. V.,Deeva E. V.,Platonova A. Yu.,Geide I. V.,Kodess M. I.,Morzherin Yu. Yu. // RUSSIAN JOURNAL OF ORGANIC CHEMISTRY. - 2009. - V. 45, l. 5. - P. 743-754.

ISSN/EISSN:

1070-4280 / нет данных

Type:

Article

Abstract:

The cyclization via the mechanism of ``tert-amino effect{''} of 2-(4-R-piperidino)benzaldehydes with cyclic active methylene components (Meldrum's acid, 1,3-cyclohexanedione, and N,N-disubstituted barbituric acids) proceeded stereoselectively giving spiro-joined 2,3,4,4a,5,6-hexahydro-1H-benzo{[}c]quinolizines with axially oriented hydrogen atoms in the positions 3 and 4a of the benzo{[}c]quinolizine ring.

Author keywords:

HYDROGEN-TRANSFER; AMINO; PYRROLO<1,2-A>QUINOLINES

DOI:

10.1134/S1070428009050170

Web of Science ID:

ISI:000266829300017

Соавторы в МНС:

Другие поля

Поле	Значение
Month	MAY
Publisher	MAIK NAUKA/INTERPERIODICA/SPRINGER
Address	233 SPRING ST, NEW YORK, NY 10013-1578 USA
Language	English
Keywords-Plus	HYDROGEN-TRANSFER; AMINO; PYRROLO<1,2-A>QUINOLINES
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Organic
Author-Email	morzherin@mail.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	13
Usage-Count-Last-180-days	1
Usage-Count-Since-2013	15
Journal-ISO	Russ. J. Organ. Chem.
Doc-Delivery-Number	456GC