A CONVENIENT SYNTHESIS OF CHIRAL N-BOC-AMINO ETHERS AS POTENTIAL PEPTIDE-BOND SURROGATE UNITS

被引:45
作者
HO, MF
CHUNG, JKK
TANG, N
机构
[1] Deparment of Medicinal Chemistry, School of Pharmacy State University of New York at Buffalo, Buffalo
关键词
D O I
10.1016/0040-4039(93)88092-W
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Boron trifluoride etherate and zinc triflate have been found ro be effective catalysts for the synthetic route to chiral N-Boc-amino ethers via a Lewis acid-catalyzed ring-opening of N-acyl aziridines, derived from chiral amino acids.
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页码:6513 / 6516
页数:4
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