facile and convenient one-pot process for the synthesis of spirooxindole derivatives in high optical purity using (?)-(s)-brevicolline as an organocatalyst简单和方便锅法合成spirooxindole衍生产品光学纯度高使用()-(s)-brevicolline organocatalyst.pdfVIP
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facile and convenient one-pot process for the synthesis of spirooxindole derivatives in high optical purity using (?)-(s)-brevicolline as an organocatalyst简单和方便锅法合成spirooxindole衍生产品光学纯度高使用()-(s)-brevicolline organocatalyst
Symmetry 2011, 3, 165-170; doi:10.3390/sym3020165
OPEN ACCESS
symmetry
ISSN 2073-8994
/journal/symmetry
Article
Facile and Convenient One-Pot Process for the Synthesis of
Spirooxindole Derivatives in High Optical Purity Using
(−)-(S)-Brevicolline as an Organocatalyst
Fliur Macaev *, Natalia Sucman, Felix Shepeli, Marina Zveaghintseva and Vsevolod Pogrebnoi
Academy Street 3, Institute of Chemistry, Academy of Science of Moldova, MD-2028 Chisinau,
Moldova; E-Mails: nicheli@yandex.ru (N.S.); dianashepel@mail.ru (F.S.); mari6azv@mail.ru (M.Z.);
seva.antivirus@ (V.P.)
* Author to whom correspondence should be addressed; E-Mail: flmacaev@cc.acad.md;
Tel.: +373-22-73-97-54; Fax: +737-22-73-99-54.
Received: 10 March 2011; in revised form: 11 April 2011 / Accepted: 12 April 2011 /
Published: 20 April 2011
Abstract: The paper presents an application of the asymmetry approach to spirooxindoles
via Brevicolline, Cinchonidine or Cinchonine catalyzed one-pot multicomponent synthesis.
Brevicolline, in comparison with Cinchonidine or Cinchonine, catalyzes the reaction of
isatins, acetylacetone/ethyl 3-oxobutanoate and malononitrile, with the formation of
spiro[oxindole-3,4-4H-pirane] derivatives in an optically active form in very good to
excellent yields.
Keywords: organocatalyzed reactions; spiro[oxindole-3,4-4H-pyrane]; Brevicolline;
Cinchonidine; Cinchonine
1. Introduction
Asymmetric catalysis with the participation of organic compounds is one of the m
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