Flexible synthetic routes to poison-frog alkaloids of the 5,8-disubstituted indolizidine-class I: synthesis of common lactam chiral building blocks and application to the synthesis of (-)-203A, (-)-205A, and (-)-219F-Reference-Cited by-同舟云学术

Flexible synthetic routes to poison-frog alkaloids of the 5,8-disubstituted indolizidine-class I: synthesis of common lactam chiral building blocks and application to the synthesis of (-)-203A, (-)-205A, and (-)-219F

Published:2007-09-28 Issue: Volume:3 Page:
ISSN:1860-5397
Container-title:Beilstein Journal of Organic Chemistry
language:en
Short-container-title:Beilstein J. Org. Chem.

Author:

Toyooka Naoki,Zhou Dejun,Nemoto Hideo,Garraffo H Martin,Spande Thomas F,Daly John W

Publisher

Beilstein Institut

Subject

Organic Chemistry

Link

https://www.beilstein-journals.org/bjoc/content/pdf/1860-5397-3-29.pdf

Reference28 articles.

1. Indolizidine and quinolizidine alkaloids

2. Alkaloids from Amphibian Skin: A Tabulation of Over Eight-Hundred Compounds

3. Nicotinic Agonists, Antagonists, and Modulators From Natural Sources

4. Enantioselective syntheses of two 5, 9E diastereomers of 223V, an alkaloid from the poison frog Dendrobates pumilio

5. Enantioselective Synthesis of Poison-Frog Alkaloid 237D and Determination of Absolute Stereochemistry

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