Highly Enantioselective Synthesis of Spiro[cyclohexanone-oxindoles] and Spiro[cyclohexanone-pyrazolones] by Asymmetric Cascade [5+1] Double Michael Reactions-Reference-Cited by-同舟云学术

Highly Enantioselective Synthesis of Spiro[cyclohexanone-oxindoles] and Spiro[cyclohexanone-pyrazolones] by Asymmetric Cascade [5+1] Double Michael Reactions

Published:2012-01-04 Issue:7 Volume:2012 Page:1318-1327
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Wu Bin,Chen Jian,Li Mei-Qiu,Zhang Jin-Xin,Xu Xiao-Ping,Ji Shun-Jun,Wang Xing-Wang

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.201101529/fullpdf

Reference88 articles.

1. Total Synthesis of SR 121463 A, a Highly Potent and Selective Vasopressin V2 Receptor Antagonist

2. Eine chemische Denksportaufgabe: die Totalsynthese von Gelsemin

3. Construction of Spiro[pyrrolidine‐3,3′‐oxindoles] − Recent Applications to the Synthesis of Oxindole Alkaloids

4. A Library of Spirooxindoles Based on a Stereoselective Three-Component Coupling Reaction

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