A-Ring Synthons of 19-Nor Type Vitamin D Derivatives

被引:2
|
作者
Akagi, Yusuke [1 ]
Yasui, Koji [1 ]
Nagasawa, Kazuo [1 ]
机构
[1] Tokyo Univ Agr & Technol, Dept Biotechnol & Engn, Fuchu, Tokyo, Japan
关键词
19-Norvitamin D; A-ring synthon; Ring-closing metathesis; Suzuki-Miyaura reaction; 1-ALPHA; 25-DIHYDROXY-19-NORVITAMIN D-3; D ANALOGS; 25-DIHYDROXYVITAMIN D-3; PRACTICAL SYNTHESIS; PRECURSORS; THERAPY;
D O I
10.1016/j.jsbmb.2016.07.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Various 19-nor vitamin D analogs, which lack the methylene group at C19, exhibit significant vitamin D (VD)-related biological activities, but generally show a reduced calcemic side-effect compared with VD itself. Among them, paricalcitol is already used clinically for treatment and prevention of secondary hyperparathyroidism associated with chronic renal failure. Therefore, considerable synthetic efforts have been directed towards 19-nor VD analogs, focusing especially on A-ring synthons suitable for use in convergent synthetic strategies based on coupling of CD-ring synthons and A-ring synthons. For example, we have recently developed a new synthetic route to A-ring synthons from linear dienes based upon a ring-closing olefin metathesis strategy. Here, we review recent synthetic approaches to A-ring synthons for 19-nor VD derivatives. (c) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:64 / 68
页数:5
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