Highly Enantiospecific Borylation for Chiral α-Amino Tertiary Boronic Esters

被引:19
作者
Qi, Qingqing [1 ]
Yang, Xuena [1 ]
Fu, Xiaoping [1 ]
Xu, Shiqing [1 ]
Negishi, Ei-ichi [1 ]
机构
[1] Purdue Univ, Herbert C Brown Labs Chem, 560 Oval Dr, W Lafayette, IN 47907 USA
关键词
alpha-aminoboronates; asymmetric synthesis; borylation; quaternary centers; rotamer; CROSS-COUPLING REACTIONS; ASYMMETRIC-SYNTHESIS; ENANTIOSELECTIVE SYNTHESIS; LITHIATION-SUBSTITUTION; STEREOSELECTIVE-SYNTHESIS; PINACOLBORYL ADDITION; ACID-DERIVATIVES; HYDROBORATION; ARYL; SECONDARY;
D O I
10.1002/anie.201809389
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Herein we report a highly efficient and enantiospecific borylation method to synthesize a wide range of enantiopure (>99% ee) alpha-amino tertiary boronic esters. The configurationally stable alpha-N-Boc substituted tertiary organo-lithium species and pinacolborane (HBpin) underwent enantiospecific borylation at 78 degrees C with the formation of a new stereogenic C-B bond. This reaction has a broad scope, enabling the synthesis of various a-amino tertiary boronic esters in excellent yields and, importantly, with universally excellent enantiospecificity (>99% es) and complete retention of configuration.
引用
收藏
页码:15138 / 15142
页数:5
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