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Asymmetric catalysis with short-chain peptides
被引:65
|作者:
Lewandowski, Bartosz
[1
]
Wennemers, Helma
[1
]
机构:
[1] ETH, Organ Chem Lab, CH-8093 Zurich, Switzerland
基金:
瑞士国家科学基金会;
关键词:
CONJUGATE ADDITION-REACTIONS;
1,4-ADDITION REACTIONS;
ENAMINE CATALYSIS;
EPOXIDATION;
ALDEHYDES;
EFFICIENT;
NITROOLEFINS;
TRIPEPTIDES;
SPACE;
D O I:
10.1016/j.cbpa.2014.09.011
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Within this review article we describe recent developments in asymmetric catalysis with peptides. Numerous peptides have been established in the past two decades that catalyze a wide variety of transformations with high stereoselectivities and yields, as well as broad substrate scope. We highlight here catalytically active peptides, which have addressed challenges that had thus far remained elusive in asymmetric catalysis: enantioselective synthesis of atropoisomers and quaternary stereogenic centers, regioselective transformations of polyfunctional substrates, chemoselective transformations, catalysis in-flow and reactions in aqueous environments.
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页码:40 / 46
页数:7
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