Uno Brice E, Dicken Rachel D, Redfern Louis R, Stern Charlotte M, Krzywicki Greg G, Scheidt Karl A
Department of Chemistry , Center for Molecular Innovation and Drug Discovery , Northwestern University , 2145 Sheridan Rd , Evanston , IL 60208 , USA . Email:
Chem Sci. 2018 Jan 10;9(6):1634-1639. doi: 10.1039/c7sc05205g. eCollection 2018 Feb 14.
The direct enantioselective chiral calcium(ii)·phosphate complex (Ca[CPA])-catalyzed conjugate addition of unprotected alkyl amines to maleimides was developed. This mild catalytic system represents a significant advance towards the general convergent asymmetric amination of α,β-unsaturated electrophiles, providing medicinally relevant chiral aminosuccinimide products in high yields and enantioselectivities. Furthermore, the catalyst can be reused directly from a previously chromatographed reaction and still maintain both high yield and selectivity.
开发了直接对映选择性手性钙(II)·磷酸盐配合物(Ca[CPA])催化的未保护烷基胺与马来酰亚胺的共轭加成反应。这种温和的催化体系代表了α,β-不饱和亲电试剂通用收敛不对称胺化反应的重大进展,能以高收率和对映选择性提供具有药用价值的手性氨基琥珀酰亚胺产物。此外,该催化剂可直接从先前经柱色谱分离的反应中重复使用,且仍能保持高收率和选择性。