A Practical and Facile Route for the Preparation of 18-Norandrostan-17-ones from Androstan-17-ones Using SmI2-Promoted Cyclization and Dehydroxylation-Reference-Cited by-同舟云学术

A Practical and Facile Route for the Preparation of 18-Norandrostan-17-ones from Androstan-17-ones Using SmI2-Promoted Cyclization and Dehydroxylation

Published:2000-05-02 Issue:11 Volume:65 Page:3555-3557
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Jiang Xin¹,Wang Cunde¹,Hu Yuefei¹,Hu Hongwen¹,Covey Douglas F.²

Affiliation:

1. Department of Chemistry, Nanjing University, Nanjing 210093, People's Republic of China

2. Department of Molecular Biology and Pharmacology, Washington University School of Medicine, St. Louis, Missouri 63110

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo991906u

Reference25 articles.

1. Enantioselective total synthesis of a protosterol, 3.beta.,20-dihydroxyprotost-24-ene

2. Steroid Total Synthesis—Hydrochrysene Approach. VII.1 Metal-in-Ammonia Reduction of the Aromatic Nucleus. dl-Epiandrosterone and the Lumi Epimer

3. SYNTHESIS OF 18,19-DINOR STEROIDS

4. SYNTHESIS OF 17,18-BISNORSTEROIDS

5. Steroid Total Synthesis—Hydrochrysene Approach. XIV.1 The Synthesis of dl-18-Norepiandrosterone and dl-18-Nortestosterone2

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