Stereoselective Synthesis of 3-Alkylideneoxindoles via Palladium-Catalyzed Domino Reactions-Reference-Cited by-同舟云学术

Stereoselective Synthesis of 3-Alkylideneoxindoles via Palladium-Catalyzed Domino Reactions

Published:2005-07-26 Issue:17 Volume:70 Page:6972-6975
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Yanada Reiko¹,Obika Shingo¹,Inokuma Tsubasa¹,Yanada Kazuo¹,Yamashita Masayuki¹,Ohta Shunsaku¹,Takemoto Yoshiji¹

Affiliation:

1. Graduate School of Pharmaceutical Sciences, Kyoto University, Yoshida, Sakyo-ku, Kyoto 606-8501, Japan, Faculty of Pharmaceutical Sciences, Setsunan University, Nagaotoge-cho, Hirakata, Osaka 573-0101, Japan, and Kyoto Pharmaceutical University, Misasagi-Nakauchicho 5, Yamashinaku, Kyoto 607-8414, Japan takemoto@pharm.kyoto-u.ac.jp

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0508604

Reference31 articles.

1. Novel Macroline Oxindoles from a Malayan Alstonia

2. The Endogenous Oxindoles 5-Hydroxyoxindole and Isatin Are Antiproliferative and Proapoptotic

3. Speradine A, a new pentacyclic oxindole alkaloid from a marine-derived fungus Aspergillus tamarii

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

5. Enantiodivergent Preparation of Optically Active Oxindoles Having a Stereogenic Quaternary Carbon Center at the C3 Position via the Lipase-Catalyzed Desymmetrization Protocol: Effective Use of 2-Furoates for Either Enzymatic Esterification or Hydrolysis

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