Total Synthesis of (−)-Histrionicotoxin through a Stereoselective Radical Translocation-Cyclization Reaction-Reference-Cited by-同舟云学术

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Total Synthesis of (−)-Histrionicotoxin through a Stereoselective Radical Translocation-Cyclization Reaction

Published:2016-12-19 Issue:4 Volume:56 Page:1087-1091
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Sato Manabu¹,Azuma Hiroki¹,Daigaku Akihiro¹,Sato Sota²³,Takasu Kiyosei¹,Okano Kentaro¹,Tokuyama Hidetoshi¹

Affiliation:

1. Graduate School of Pharmaceutical Sciences; Tohoku University; Aoba 6-3, Aramaki, Aoba-ku Sendai 980-8578 Japan

2. ERATO, Isobe Degenerate π-Integration Project and Advanced Institute for Materials Research (AIMR); 2-1-1 Katahira, Aoba-ku Sendai 980-8577 Japan

3. AIMR and Department of Chemistry; Tohoku University; Aoba 6-3, Aramaki, Aoba-ku Sendai 980-8578 Japan

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/anie.201609941/fullpdf

Reference46 articles.

1. Histrionicotoxins: Roentgen-Ray Analysis of the Novel Allenic and Acetylenic Spiroalkaloids Isolated from a Colombian Frog, Dendrobates histrionicus

2. Total Synthesis and Electrophysiological Properties of Natural (?)-Perhydrohistrionicotoxin, its Unnatural (+)-Antipode and their 2-Depentyl Analogs

3. Probes for a Regulatory Site on the Nicotinic Acetylcholine Receptor-Channel. Synthesis of (±)-7-Debutylperhydrohistrionicotoxin, (±)-2-Depentyl-7-debutylperhydrohistrionicotoxin, and their Analogues

4. Thirty-five years of synthetic studies directed towards the histrionicotoxin family of alkaloids

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2. Towards a General Access to 1‐Azaspirocyclic Systems via Photoinduced, Reductive Decarboxylative Radical Cyclizations;Chemistry – A European Journal;2024-01-12

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