Reverse Aromatic Cope Rearrangement of 2-Allyl-3-alkylideneindolines Driven by Olefination of 2-Allylindolin-3-ones: Synthesis of α-Allyl-3-indole Acetate Derivatives-Reference-Cited by-同舟云学术

Reverse Aromatic Cope Rearrangement of 2-Allyl-3-alkylideneindolines Driven by Olefination of 2-Allylindolin-3-ones: Synthesis of α-Allyl-3-indole Acetate Derivatives

Published:2001-01-30 Issue:4 Volume:66 Page:1200-1204
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Kawasaki Tomomi¹,Nonaka Yoshinori¹,Watanabe Kazuaki¹,Ogawa Atsuyo¹,Higuchi Kazuhiro¹,Terashima Romi¹,Masuda Kouhei¹,Sakamoto Masanori¹

Affiliation:

1. Meiji Pharmaceutical University, 2-522-1, Noshio, Kiyose, Tokyo 204-8688, Japan, and Kissei Pharmaceutical Co., Ltd., Discovery Research, R & D, 4365-1, Kashiwabara, Hotaka, Minamiazumi, Nagano 399-8304, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0014921

Reference34 articles.

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2. Tandem Cope-Claisen rearrangement. Scope and stereochemistry

3. Thio-Claisen and Cope rearrangements. A general method for the synthesis of .alpha.,.beta.,.alpha.,.zeta.-unsaturated thioamides

4. Tandem Asymmetric Cyclopropanation/Cope Rearrangement. A Highly Diastereoselective and Enantioselective Method for the Construction of 1,4-Cycloheptadienes

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