Synthesis of Chiral Saturated Heterocycles Bearing Quaternary Centers via Enantioselective β-C(sp3)-H Activation of Lactams

被引:1
作者
Lu, Peng [1 ]
Burgenson, William R. [1 ]
Simmons, Bryan J. [2 ]
Liu, Shuang [2 ]
Yeung, Kap-Sun [3 ]
Qiao, Jennifer X. [3 ]
Yu, Jin-Quan [1 ]
机构
[1] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
[2] Bristol Myers Squibb, Res & Dev, San Diego, CA 92121 USA
[3] Bristol Myers Squibb, Res & Dev, Cambridge, MA 02141 USA
关键词
CONSTRUCTION; THALIDOMIDE;
D O I
10.1021/jacs.4c15834
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of catalytic methods for the synthesis of enantiopure saturated heterocycles has been a long-standing challenge in asymmetric catalysis. We describe the first highly enantioselective palladium-catalyzed beta-C(sp3)-H arylation and olefination of lactams for the preparation of various chiral N-heterocycles bearing quaternary carbon centers. The presence of strongly electron-withdrawing groups on the chiral bifunctional MPAThio ligand is crucial to the reactivity of weakly coordinating lactams. The resulting enantioenriched lactams are readily converted to a family of chiral piperidines and imides that are highly desirable in drug discovery.
引用
收藏
页码:1427 / 1433
页数:7
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