Efficient and Versatile Synthesis of Novel 2α-Substituted 1α,25-Dihydroxyvitamin D3 Analogues and Their Docking to Vitamin D Receptors-Reference-Cited by-同舟云学术

Efficient and Versatile Synthesis of Novel 2α-Substituted 1α,25-Dihydroxyvitamin D3 Analogues and Their Docking to Vitamin D Receptors

Published:2001-11-27 Issue:26 Volume:66 Page:8760-8771
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Suhara Yoshitomo¹,Nihei Ken-ichi¹,Kurihara Masaaki¹,Kittaka Atsushi¹,Yamaguchi Kentaro¹,Fujishima Toshie¹,Konno Katsuhiro¹,Miyata Naoki¹,Takayama Hiroaki¹

Affiliation:

1. Faculty of Pharmaceutical Sciences, Teikyo University, Sagamiko, Kanagawa 199-0195, Japan, National Institute of Health Sciences, Kamiyoga, Setagaya-ku, Tokyo 158-8501, Japan, and Chemical Analytical Center, Chiba University, Inage-ku, Chiba 263-8522, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo010375i

Reference22 articles.

1. The vitamin D endocrine system and its therapeutic potential

2. Novel nonsecosteroidal vitamin D mimics exert VDR-modulating activities with less calcium mobilization than 1,25-dihydroxyvitamin D3

3. A novel and practical route to A-ring enyne synthon for 1α,25-dihydroxyvitamin D3 analogs: Synthesis of A-ring diastereomers of 1α,25-dihydroxyvitamin D3 and 2-methyl-1,25-dihydroxyvitamin D3

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