Asymmetric Cleavage of 9-Azabicyclo[3.3.1]nonan-3-one intocis-2,6-Disubstituted Piperidine. A Facile Approach to a Chiral Building Block for Alkaloid Synthesis-Reference-Cited by-同舟云学术

Asymmetric Cleavage of 9-Azabicyclo[3.3.1]nonan-3-one intocis-2,6-Disubstituted Piperidine. A Facile Approach to a Chiral Building Block for Alkaloid Synthesis

Published:1990-08 Issue:8 Volume:19 Page:1319-1322
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Momose Takefumi,Toyooka Naoki,Hirai Yoshiro

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/cl/19/8/19_8_1319/_pdf

Reference15 articles.

1. Bicyclo[3.3.1]nonanes as synthetic intermediates. IV. Behavior of bicyclo[3.n.1]alkan-3-ones toward the Baeyer-Villiger oxidation.

2. An Azabycyclo[3.3.1]nonanone Apprpach to Tecoma Alkaloids: A Stereoselective Synthesis of (±)-7-Demethyltecomanine

3. Enantioselective deprotonation by chiral lithium amide bases: asymmetric synthesis of trimethylsilyl enol ethers from 4-alkylcyclohexanones

4. Enantioselective deprotonation of the monoacetals of bicyclo[3.3.0]octan-3,7-dione. An approach to the asymmetric synthesis of chiral synthons for carbacyclins

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