A highly enantioselective acyl-Mannich reaction of isoquinolines with aldehydes promoted by proline derivatives: an approach to 13-alkyl-tetrahydroprotoberberine alkaloids-Reference-Cited by-同舟云学术

A highly enantioselective acyl-Mannich reaction of isoquinolines with aldehydes promoted by proline derivatives: an approach to 13-alkyl-tetrahydroprotoberberine alkaloids

Published:2014-06-30 Issue:10 Volume:5 Page:3915
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Mengozzi L.,Gualandi A.,Cozzi P. G.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/SC/C4SC01221F

Reference68 articles.

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2. Antibacterial activity and structure-activity relationships of berberine analogs

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4. Corydaline Inhibits Multiple Cytochrome P450 and UDP-Glucuronosyltransferase Enzyme Activities in Human Liver Microsomes

5. A regioselective entry to 13-substituted 8-oxoprotoberberines. Total synthesis of (.+-.)-corydaline

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