STEREOSELECTION IN THE REACTION OF ACID HALIDES AND VINYLOGOUS URETHANES

被引：5
作者：
SCHLESSINGER, RH [1 ]
TATA, JR [1 ]
SPRINGER, JP [1 ]
机构：
[1] MERCK SHARP & DOHME RES LABS, RAHWAY, NJ 07065 USA
来源：
TETRAHEDRON LETTERS | 1987年 / 28卷 / 45期
关键词：
D O I：
10.1016/S0040-4039(00)96744-3
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Acid halides which carry either an α-phenyl or α-alkoxy residue show fascinatingly high and useful diastereoselection on condensation with the vinylogous urethane derived ketene acetal enamine 3. Optically active halides of this type undergo reaction with 3 accompanied by very high diastereofacial selectivity. © 1987.
引用
收藏
页码：5423 / 5426
页数：4
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