Enantioselective catalytic lithiation using a chiral binaphthyl derivative as electron carrier

被引:3
|
作者
Martinez, Regina
Pastor, Isidro M. [1 ]
Yus, Miguel
机构
[1] Univ Alicante, Fac Ciencias, Dept Quim Organ, Apdo 99, Alicante 03080, Spain
关键词
Lithium metal; stereoselectivity; binaphthyl derivatives; arene catalyzed lithiation; FUNCTIONALIZED ORGANOLITHIUM COMPOUNDS; NON-DEPROTONATING METHODOLOGIES; HETEROCYCLES; SYNTHONS; LIGANDS;
D O I
10.3998/ark.5550190.p008.192
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The lithiation, of the secondary chloride 2, catalyzed by binaphthyl derivatives, i.e. BINAM 4, BINOL 5, BINAP 6, H8-BINAP 7, Tol-BINAP 8, 2,2'-bis(pyrrolidin-1-yl)-1,1'-binaphthalene 9, and 2,2'-dimethyl-1,1'-binaphthalene 11, in the presence of different ketones has been studied, yielding the corresponding alcohol derivatives 3 and 12-16 in moderate to good yields. Binaphthyl derivative 11 has revealed to be very active as catalyst in the lithiation process at room temperature, and has allowed the preparation of the alcohol derivatives with enantioselectivities up to 50%.
引用
收藏
页码:71 / 84
页数:14
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