Stereoselective synthesis of spirofused 3-substituted 2,3,4,4a,5,6-hexahydro-6H-benzo[c]quinolizine using the tert-amino effect

Stereoselective synthesis of spirofused 3-substituted 2,3,4,4a,5,6-hexahydro-6H-benzo[c]quinolizine using the tert-amino effect Full article

Journal

Mendeleev Communications
ISSN: 0959-9436

Output data

Year: 2006, Volume: 16, Number: 2, Pages: 82-83 Pages count : 2 DOI: 10.1070/MC2006v016n02ABEH002247

Authors

Deeva Elisaveta V. ¹ , Glukhareva Tatiana V. ¹ , Tkachev Alexey V. ² , Morzherin Yury Yu. ¹

Affiliations

1	(Данные Web of science) Urals State Tech Univ, Dept Technol Organ Synth, Ekaterinburg 620002, Russia
2	(Данные Web of science) Russian Acad Sci, Siberian Branch, NN Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia

The interaction of 2-(4-R-piperidino)benzaldehyde and cyclic CH-active compounds occurred as a tandem of Knovenagel condensation and cyclization by tert-amino effect and led to spiro-fused 3-substituted 2,3,4,4a,5,6-hexahydro-6H-benzo[c]quinolizine.

Deeva E.V. , Glukhareva T.V. , Tkachev A.V. , Morzherin Y.Y.
Stereoselective synthesis of spirofused 3-substituted 2,3,4,4a,5,6-hexahydro-6H-benzo[c]quinolizine using the tert-amino effect
Mendeleev Communications. 2006. V.16. N2. P.82-83. DOI: 10.1070/MC2006v016n02ABEH002247 WOS Scopus РИНЦ OpenAlex

Published print:

Jan 1, 2006

Web of science:	WOS:000237698300010
Scopus:	2-s2.0-33744501303
Elibrary:	13504372
OpenAlex:	W2178122999

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