Diastereo- and Enantioselective [3 + 2] Cycloaddition Reaction of Morita–Baylis–Hillman Carbonates of Isatins with N-Phenylmaleimide Catalyzed by Me-DuPhos-Reference-Cited by-同舟云学术

Diastereo- and Enantioselective [3 + 2] Cycloaddition Reaction of Morita–Baylis–Hillman Carbonates of Isatins with N-Phenylmaleimide Catalyzed by Me-DuPhos

Published:2012-04-10 Issue:8 Volume:77 Page:4143-4147
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Wang Yan¹²,Liu Li¹,Zhang Tao¹²,Zhong Neng-Jun¹²,Wang Dong¹,Chen Yong-Jun¹

Affiliation:

1. Beijing National Laboratory for Molecular Sciences (BNLMS), CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China

2. Graduate School of Chinese Academy of Sciences, Beijing 100049, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo3002535

Reference43 articles.

1. Paraherquamides, Brevianamides, and Asperparalines: Laboratory Synthesis and Biosynthesis. An Interim Report

2. Gelsemine: A Thought-Provoking Target for Total Synthesis

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

4. Pyrrolidinyl-Spirooxindole Natural Products as Inspirations for the Development of Potential Therapeutic Agents

5. Asymmetric Syntheses of Oxindole and Indole Spirocyclic Alkaloid Natural Products

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