Synthesis of 4-alkyl-1-benzhydryl-2-(methoxymethyl)azetidin-3-ols by regio- and stereoselective alkylation of 1-benzhydryl-3-(N-alkyl)imino-2-(methoxymethyl)azetidine-Reference-Cited by-同舟云学术

Synthesis of 4-alkyl-1-benzhydryl-2-(methoxymethyl)azetidin-3-ols by regio- and stereoselective alkylation of 1-benzhydryl-3-(N-alkyl)imino-2-(methoxymethyl)azetidine

Published:2002-04 Issue:14 Volume:58 Page:2763-2775
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Salgado Antonio,Boeykens Mark,Gauthier Christine,Declercq Jean-Paul,De Kimpe Norbert

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference71 articles.

1. Penaresidin A and B, two novel azetidine alkaloids with potent actomyosin ATPase-activating activity from the Okinawan marine sponge Penares sp.

2. Synthesis of sphingosine relatives. Part 19.1 Synthesis of penaresidin A and B, azetidine alkaloids with actomyosin ATPase-activating properties

3. Synthesis of a straight chain analog of penaresidins, azetidine alkaloids from marine sponge penares sp.

4. Synthesis of penaresidin a, an azetidine alkaloid with actomyosin ATPase-activating property

5. Absolute stereochemistry of penaresidins A and B

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