Eine asymmetrische organokatalytische Domino-Michael-Aldol- Reaktion: enantioselektiver Zugang zu chiralen Cycloheptanonen, Tetrahydrochromenonen und polyfunktionalisierten Bicyclo[3.2.1]octanen-Reference-Cited by-同舟云学术

Eine asymmetrische organokatalytische Domino-Michael-Aldol- Reaktion: enantioselektiver Zugang zu chiralen Cycloheptanonen, Tetrahydrochromenonen und polyfunktionalisierten Bicyclo[3.2.1]octanen

Published:2009-05-04 Issue:20 Volume:121 Page:3754-3757
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Rueping Magnus,Kuenkel Alexander,Tato Francisco,Bats Jan W.

Publisher

Wiley

Subject

General Medicine

Reference111 articles.

1. Ausgewählte Beispiele für die Verwendung von 1,2-Dionen in der organischen Synthese:

2. Radical Cyclisation Reactions Leading to Polycyclics Related to the Amaryllidaceae and Erythrina Alkaloids

3. Bisoxazolidine-Catalyzed Enantioselective Alkynylation of Aldehydes

4. A ‘one pot’ microwave-mediated synthesis of the basic canthine skeleton: expedient access to unnatural β-carboline alkaloids

5. Conformationally restrained carbazolone-containing α,γ-diketo acids as inhibitors of HIV integrase

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