Flexible synthesis of poison-frog alkaloids of the 5,8-disubstituted indolizidine-class. II: Synthesis of (-)-209B, (-)-231C, (-)-233D, (-)-235B", (-)-221I, and an epimer of 193E and pharmacological effects at neuronal nicotinic acetylcholine receptors-Reference-Cited by-同舟云学术

Flexible synthesis of poison-frog alkaloids of the 5,8-disubstituted indolizidine-class. II: Synthesis of (-)-209B, (-)-231C, (-)-233D, (-)-235B", (-)-221I, and an epimer of 193E and pharmacological effects at neuronal nicotinic acetylcholine receptors

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:

Kobayashi Soushi,Toyooka Naoki,Zhou Dejun,Tsuneki Hiroshi,Wada Tsutomu,Sasaoka Toshiyasu,Sakai Hideki,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/1860-5397-3-30.pdf

Reference19 articles.

1. 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

2. 5,8-Disubstituted indolizidines: A new class of noncompetitive blockers for nicotinic receptor-channels

3. Alkaloids Indolizidine 235B′, Quinolizidine 1-epi-207I, and the Tricyclic 205B are Potent and Selective Noncompetitive Inhibitors of Nicotinic Acetylcholine Receptors

4. Brain nicotinic acetylcholine receptors: native subtypes and their relevance

5. Nicotinic Acetylcholine Receptors and Nicotinic Cholinergic Mechanisms of the Central Nervous System

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