Lactam Strategy Using Amide-Selective Nucleophilic Addition for Quick Access to Complex Amines: Unified Total Synthesis of Stemoamide-Type Alkaloids-Reference-Cited by-同舟云学术

Lactam Strategy Using Amide-Selective Nucleophilic Addition for Quick Access to Complex Amines: Unified Total Synthesis of Stemoamide-Type Alkaloids

Published:2022-02-15 Issue:2 Volume:95 Page:278-287
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Sugiyama Yasukazu¹,Soda Yasuki¹,Yoritate Makoto¹,Tajima Hayato¹,Takahashi Yoshito¹,Shibuya Kana¹,Ogihara Chisato¹,Yokoyama Takashi¹,Oishi Takeshi²,Sato Takaaki¹,Chida Noritaka¹

Affiliation:

1. Department of Applied Chemistry, Faculty of Science and Technology, Keio University, 3-14-1 Hiyoshi, Kohoku-ku, Yokohama, Kanagawa 223-8522, Japan

2. School of Medicine, Keio University, 4-1-1 Hiyoshi, Kohoku-ku, Yokohama, Kanagawa 223-8521, Japan

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

http://www.journal.csj.jp/doi/pdf/10.1246/bcsj.20210372

Reference129 articles.

1. For a recent and selected book on efficient total synthesis, see: P.Q. Huang, Z.J. Yao, R. P. Hsung, Efficiency in Natural Product Total Synthesis, Wiley, Hoboken, 2018.

2. A Longitudinal Study of Alkaloid Synthesis Reveals Functional Group Interconversions as Bad Actors

3. Generation of Secondary, Tertiary, and Quaternary Centers by Geminal Disubstitution of Carbonyl Oxygens

4. Thioamides and Thioformamides for Sequential Reactions with Organolithium and Grignard Reagents

5. Nucleophilic addition to N-alkoxyamides

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