The synthesis and stereochemistry of (22R)-20α,22- and (22S)-20α,22-dihydroxycholesterol
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Clinical Biochemistry,Pharmacology,Endocrinology,Molecular Biology,Biochemistry
Cited by 34 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Stereoselective synthesis of (22R)- and (22S)-castasterone/ponasterone A hybrid compounds and evaluation of their molting hormone activity;Steroids;2004-07
2. Stereoselective reactions of (20R)-3,20-dihydroxy-(3′,4′-dihydro-2′H-pyranyl)-5-pregnene derivatives form 27-nor-3,20,23,26-tetrahydroxy-cholesten-22-ones and related bromo ketones;Steroids;2004-01
3. Synthesis of a Castasterone/Ponasterone Hybrid Compound and Evaluation of Its Molting Hormone-Like Activity;Journal of Pesticide Science;2003
4. An improved synthesis of (20R,22R)-cholest-5-ene-3β,20,22-triol, an intermediate in steroid hormone formation and an activator of nuclear orphan receptor LXRα;Steroids;1999-06
5. Alternative Access to 20-Hydroxyecdysteroid Side Chain by Means of Samarium Iodide-promoted Radical Addition of Tetrahydrofuran to a 20-Keto Steroid;HETEROCYCLES;1998
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