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REGIOSELECTIVE AND STEREOSELECTIVE TRITIATION OF THE JUVENOID ANALOG W-328

被引：3
作者：
ELBERT, T
CERNY, B
WIMMER, Z
SERGENT, L
机构：
[1] ACAD SCI CZECH REPUBLIC, INST ORGAN CHEM & BIOCHEM, CS-16610 PRAGUE 6, CZECHOSLOVAKIA
[2] CENS, SERV MOLEC MARQUEES, F-91191 GIF SUR YVETTE, FRANCE
来源：
COLLECTION OF CZECHOSLOVAK CHEMICAL COMMUNICATIONS | 1993年 / 58卷 / 05期
关键词：
D O I：
10.1135/cccc19931164
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
The juvenoid analog 2-(4-(2-(ethoxycarbamato)ethoxy)benzyl)-1-cyclohexanone ethylene acetal (I) (W 328) was labelled by H-3 in the benzyl position by the CESG method. H-3 NMR revealed the stereoselectivity of the labelling. The results are compared with the data published in the literature and discussed in the terms of stereoelectronic requirements.
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页码：1164 / 1168
页数：5
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