Lewis Base/3d Transition-Metal Cooperatively Catalyzed Asymmetric Reactions

被引:6
作者
Song, Jin [1 ]
Gong, Liu-Zhu [2 ,3 ]
机构
[1] Anhui Univ, Inst Phys Sci & Informat Technol, Key Lab Environm Friendly Polymer Mat Anhui Prov, Hefei 230601, Peoples R China
[2] Univ Sci & Technol China, Hefei Natl Res Ctr Phys Sci Microscale, Hefei 230026, Peoples R China
[3] Univ Sci & Technol China, Dept Chem, Hefei 230026, Peoples R China
基金
中国国家自然科学基金;
关键词
Lewis bases; 3d transition metals; cooperative catalysis; asymmetric catalysis; stereodivergent synthesis; N-HETEROCYCLIC CARBENE; SYNERGISTIC CATALYSIS; ALPHA-ALLYLATION; ANNULATION; ESTERS; NHC; ENANTIOSELECTIVITY; BENZOTETRAMISOLE; ALKYLATION; ACTIVATION;
D O I
10.1055/a-2192-9185
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Lewis base/transition-metal cooperatively catalyzed asymmetric transformations have attracted extensive attention as they offer complementary catalytic systems within the realm of cooperative catalysis. Recently, the synergistic use of Lewis bases in combination with earth-abundant 3d metals has emerged as a fascinating prospect, presenting an opportunity to move away from the reliance on noble metals and to explore novel catalytic processes. In this Account, we highlight our recent achievements regarding the chemistry and synthetic utility of isothiourea (ITU) activated C1-ammonium enolates and N -heterocyclic carbene (NHC)-bound homoenolate equivalents in conjunction with 3d transition-metal activated electrophiles. The remarkable success in the stereoselective construction of carbon-carbon and carbon- heteroatom bonds has led to significant contributions to stereodivergent synthesis.
引用
收藏
页码:1621 / 1628
页数:8
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