Stereospecific introduction of 3α-methoxy group to the versatile intermediate of 11-oxygenated ethanophenanthridine alkaloids. Total syntheses of (±)-crinamine, (±)-6-hydroxycrinamine, (±)-criwelline, and (±)-macronine.-Reference-Cited by-同舟云学术

Stereospecific introduction of 3α-methoxy group to the versatile intermediate of 11-oxygenated ethanophenanthridine alkaloids. Total syntheses of (±)-crinamine, (±)-6-hydroxycrinamine, (±)-criwelline, and (±)-macronine.

Published:1976-07 Issue:27 Volume:17 Page:2331-2334
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Isobe Kimiaki,Taga Jun'ichi,Tsuda Yoshisuke

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference5 articles.

1. Stereoselective total synthesis of the alkaloid haemanthamine

2. Total syntheses of the alkaloids haemanthidine and tazettine

3. Electrophilic organoselenium reagents. New route to allylic acetates and ethers

4. The Amaryllidaceae alkaloids;Wildman;The Alkaloids,1968

5. Y. Tsuda, T. Sano, and H. Watanabe, Synthesis, to be published.

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