Enantioselective Synthesis of 3,4-Dihydropyran-2-ones by Domino Michael Addition and Lactonization with New Asymmetric Organocatalysts: Cinchona-Alkaloid-Derived Chiral Quaternary Ammonium Phenoxides-Reference-Cited by-同舟云学术

Enantioselective Synthesis of 3,4-Dihydropyran-2-ones by Domino Michael Addition and Lactonization with New Asymmetric Organocatalysts: Cinchona-Alkaloid-Derived Chiral Quaternary Ammonium Phenoxides

Published:2007-01-08 Issue:1 Volume:2 Page:123-134
ISSN:1861-4728
Container-title:Chemistry – An Asian Journal
language:en
Short-container-title:Chem. Asian J.

Author:

Tozawa Takashi,Nagao Hitoshi,Yamane Yoshinobu,Mukaiyama Teruaki

Publisher

Wiley

Subject

General Chemistry,Biochemistry,Organic Chemistry

Reference36 articles.

1. Katalytische asymmetrische Hetero-Diels-Alder-Reaktionen von Carbonylverbindungen und Iminen

2. Catalytic Asymmetric Hetero-Diels–Alder Reactions of Carbonyl Compounds and Imines

3. Experimental and Theoretical Studies on the Hydrogen-Bond-Promoted Enantioselective Hetero-Diels−Alder Reaction of Danishefsky's Diene with Benzaldehyde

4. Transformations of Eburicoic Acid. IV. Side-Chain Degradation to 14-Methylpregnane Derivatives

5. Synthesis of 3-aryl- or 3-alkenyl-4,6-dimethyl-2-pyrones by silver ion promoted rearrangement of 4-aryl- or4-alkenyl-3-bromo-4,6-dimethyl-3,4-dihydro-2-pyrones

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