Highly enantioselective aldol reaction of acetaldehyde and isatins only with 4-hydroxydiarylprolinol as catalyst: concise stereoselective synthesis of (R)-convolutamydines B and E, (−)-donaxaridine and (R)-chimonamidine-Reference-Cited by-同舟云学术

Highly enantioselective aldol reaction of acetaldehyde and isatins only with 4-hydroxydiarylprolinol as catalyst: concise stereoselective synthesis of (R)-convolutamydines B and E, (−)-donaxaridine and (R)-chimonamidine

Published:2010-02 Issue:7 Volume:66 Page:1441-1446
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Chen Wen-Bing,Du Xi-Lin,Cun Lin-Feng,Zhang Xiao-Mei,Yuan Wei-Cheng

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference67 articles.

1. Convolutamides A ∼ F, novel γ-lactam alkaloids from the marine bryozoan Amathia convoluta

2. Convolutamydine A, a novel bioactive hydroxyoxindole alkaloid from marine bryozoan Amathia convoluta

3. Isolation and structure of convolutamydines B ∼ D from marine bryozoan Amathia convoluta

4. Three New Alkaloids, Convolutamines F and G, and Convolutamydine E, from the Floridian Marine Bryozoan Amathia convoluta

5. Synthesis of 3-aryl-3-hydroxypyrrolidin-2-ones and 2-benzyl-9b-hydroxy-3,3a,5,9b-tetrahydro-2H-pyrrolo[3,4-c]quinoline-1,4-dione derivatives from the Baylis–Hillman adducts of isatins

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