Stereospecific Stille Cross-Couplings Using Mn(II)Cl2

被引:11
|
作者
Dakarapu, Rambabu [1 ]
Falck, John R. [1 ]
机构
[1] Univ Texas Southwestern Med Ctr Dallas, Dept Biochem, Div Chem, Dallas, TX 75390 USA
来源
JOURNAL OF ORGANIC CHEMISTRY | 2018年 / 83卷 / 03期
关键词
TIN-LITHIUM EXCHANGE; ASYMMETRIC-SYNTHESIS; GRIGNARD-REAGENTS; ORGANOSTANNANES; STEREOCENTERS; MANGANESE(II); CONSTRUCTION; ALKYLATION; MECHANISMS; COPPER(I);
D O I
10.1021/acs.joc.7b02780
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Cross-coupling reactions are a staple in organic synthesis, especially for C-C bond formation with sp-and sp(2)-carbon electrophiles. In recent years, the range of accessible C-C bonds has been extended to stereogenic centers which expedites access to greater molecular complexity. However, these reactions predominantly depend upon late transition metal (LTM) catalysts whose cost, toxicity, and/or environmental impact have come under increasing scrutiny and governmental regulation. Here, we report Mn (II) Cl-2 complexes valone, or with assistance from copper, catalyze the stereospecific cross-coupling of alpha-alkoxyalkylstannanes with organic electrophiles with complete retention of configuration.
引用
收藏
页码:1241 / 1251
页数:11
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