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DOI10.1126/science.aaz7381
Biocatalytic synthesis of planar chiral macrocycles
Gagnon C.; Godin É.; Minozzi C.; Sosoe J.; Pochet C.; Collins S.K.
发表日期2020
ISSN0036-8075
起始页码917
结束页码921
卷号367期号:6480
英文摘要Macrocycles can restrict the rotation of substituents through steric repulsions, locking in conformations that provide or enhance the activities of pharmaceuticals, agrochemicals, aroma chemicals, and materials. In many cases, the arrangement of substituents in the macrocycle imparts an element of planar chirality. The difficulty in predicting when planar chirality will arise, as well as the limited number of synthetic methods to impart selectivity, have led to planar chirality being regarded as an irritant. We report a strategy for enantio- and atroposelective biocatalytic synthesis of planar chiral macrocycles. The macrocycles can be formed with high enantioselectivity from simple building blocks and are decorated with functionality that allows one to further modify the macrocycles with diverse structural features. © 2020 American Association for the Advancement of Science. All rights reserved.
关键词biochemical compositionbiochemistrycatalystenzymeenzyme activitymolecular analysisarticlebiocatalystchiralityenantioselectivitysynthesis
语种英语
来源机构Science
文献类型期刊论文
条目标识符http://gcip.llas.ac.cn/handle/2XKMVOVA/133700
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GB/T 7714
Gagnon C.,Godin É.,Minozzi C.,et al. Biocatalytic synthesis of planar chiral macrocycles[J]. Science,2020,367(6480).
APA Gagnon C.,Godin É.,Minozzi C.,Sosoe J.,Pochet C.,&Collins S.K..(2020).Biocatalytic synthesis of planar chiral macrocycles.,367(6480).
MLA Gagnon C.,et al."Biocatalytic synthesis of planar chiral macrocycles".367.6480(2020).
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