Site-Selective Reactions with Peptide-Based Catalysts

被引:49
|
作者
Giuliano, Michael W. [1 ]
Miller, Scott J. [1 ]
机构
[1] Yale Univ, Dept Chem, 225 Prospect St, New Haven, CT 06520 USA
来源
SITE-SELECTIVE CATALYSIS | 2016年 / 372卷
关键词
Asymmetric synthesis; Catalysis; Natural products; Peptides; Site-selective reactions; ALA-D-LAC; CONFORMATION-ACTIVITY RELATIONSHIPS; POLYKETIDE NATURAL-PRODUCTS; KINETIC RESOLUTION; ASYMMETRIC PHOSPHORYLATION; ENANTIOSELECTIVE SYNTHESIS; RADICAL DEOXYGENATION; ERYTHROMYCIN-A; REENGINEERING VANCOMYCIN; REMOTE STEREOCONTROL;
D O I
10.1007/128_2015_653
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The problem of catalyst-controlled site-selectivity can potentially require a catalyst to overcome energetic barriers larger than those associated with enantioselective reactions. This challenge is a signature of substrates that present reactive sites that are not of equivalent reactivity. Herein we present a narrative of our laboratory's efforts to overcome this challenge using peptide-based catalysts. We highlight the interplay between understanding the inherent reactivity preferences of a given target molecule and the development of catalysts that can overcome intrinsic preferences embedded within a substrate.
引用
收藏
页码:157 / 201
页数:45
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