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A novel method for the synthesis of maxacalcitol
Russian Journal of General Chemistry ( IF 0.9 ) Pub Date : 2016-02-18 , DOI: 10.1134/s1070363216010278
W.-Q. Song , Y.-H. Wang , D.-N. Liu , W.-Z. Fang , Q. Lu

Maxacalcitol (1), a kind of active vitamin D drugs, was prepared from pregnenolone acetate (2) using a novel synthetic method including the combination of five-step organic transformations and one-step biological transformation. The new protocol was shorter, milder, and simpler than the reported approaches. The unoptimized overall yield was 0.178%. The structure of all intermediates and final product was confirmed by 1H NMR, 13C NMR and MS techniques.

中文翻译:

合成马沙骨化醇的新方法

马沙骨化醇(1),一种活性的维生素d药物,由孕烯醇酮乙酸酯(制备2使用新的合成方法,包括五步有机转化和一步生物转化的组合)。新协议比已报道的方法更短,更温和,更简单。未优化的总产率为0.178%。所有中间体和最终产物的结构通过1 H NMR,13 C NMR和MS技术确认。
更新日期:2016-02-18
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