Sulfur(vi) fluorides as tools in biomolecular and medicinal chemistry

被引:53
作者
Carneiro, Sabrina N. [1 ]
Khasnavis, Samuel R. [1 ]
Lee, Jisun [2 ]
Butler, Todd W. [2 ]
Majmudar, Jaimeen D. [3 ]
Am Ende, Christopher W. [2 ]
Ball, Nicholas D. [1 ]
机构
[1] Pomona Coll, Dept Chem, Claremont, CA 91711 USA
[2] Pfizer Worldwide Res, Dev, Groton, CT 06340 USA
[3] Pfizer Worldwide Res & Dev, Cambridge, MA 02139 USA
基金
美国国家卫生研究院;
关键词
SUFEX CLICK CHEMISTRY; AROMATIC SULFONYL FLUORIDES; PORCINE PANCREATIC ELASTASE; IRREVERSIBLE INHIBITORS; CATHEPSIN-G; REACTIVITY; SITE; FLUOROSULFATE; CHYMOTRYPSIN; CONVENIENT;
D O I
10.1039/d2ob01891h
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Recent advances in the synthesis of sulfur(vi)-fluorides has enabled incredible growth in their application in biomolecular chemistry. This review aims to serve as a primer highlighting synthetic strategies toward a diversity of S(vi) fluorides and their application in chemical biology, bioconjugation, and medicinal chemistry.
引用
收藏
页码:1356 / 1372
页数:17
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