Total Synthesis of (−)-Hippodamine by Stereocontrolled Construction of Azaphenalene Skeleton Based on Extended One-Pot Asymmetric Azaelectrocyclization-Reference-Cited by-同舟云学术

Total Synthesis of (−)-Hippodamine by Stereocontrolled Construction of Azaphenalene Skeleton Based on Extended One-Pot Asymmetric Azaelectrocyclization

Published:2013-05-21 Issue:11 Volume:15 Page:2758-2761
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Fujita Shintaro¹,Sakaguchi Taku¹,Kobayashi Toyoharu¹,Tsuchikawa Hiroshi¹,Katsumura Shigeo¹

Affiliation:

1. School of Science and Technology, Kwansei Gakuin University, Gakuen 2-1, Sanda, Hyogo 669-1337, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol4010917

Reference30 articles.

1. Hemorrhage in a Coccinellid Beetle and Its Repellent Effect on Ants

2. Chemical ecology of arthropods—X

3. A defense alkaloid in a carnivorous beetle

4. Two Novel Alkaloids from the American Ladybug Hippodamia Convergens (Coleoptera, Coccinellidae)

5. Chemical ecology of arthropods. ix. Structure and absolute configuration of hippodamine and convergine, two novel alkaloids from the american ladybug (coleoptera - coccinellidae).

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