“Symmetry” in the synthesis of the a-ring of a vitamin D hybrid analogue with significant transactivation activity: A combinatorial sequence of regioselective propiolate-ene, catalytic enantioselective epoxidation and carbonyl-ene cyclization reactions-Reference-Cited by-同舟云学术

“Symmetry” in the synthesis of the a-ring of a vitamin D hybrid analogue with significant transactivation activity: A combinatorial sequence of regioselective propiolate-ene, catalytic enantioselective epoxidation and carbonyl-ene cyclization reactions

Published:1998-05 Issue:21 Volume:39 Page:3359-3362
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Mikami Koichi,Osawa Ayako,Isaka Akira,Sawa Eiji,Shimizu Masaki,Terada Masahiro,Kubodera Noboru,Nakagawa Kimie,Tsugawa Naoko,Okano Toshio

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference52 articles.

1. Synthesis of Vitamin D (Calciferol)

2. Synthetic Approaches to Vitamin D

3. The vitamin D endocrine system and its therapeutic potential

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