Nickel-catalyzed enantioselective hydrovinylation of silyl-protected allylic alcohols:An efficient access to homoallylic alcohols with a chiral quaternary center  被引量:1

Nickel-catalyzed enantioselective hydrovinylation of silyl-protected allylic alcohols:An efficient access to homoallylic alcohols with a chiral quaternary center

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作  者:ZHANG Qi,ZHU Shou-Fei,CAI Yan,WANG Li-Xin & ZHOU Qi-Lin State Key Laboratory and Institute of Elemento-organic Chemistry,Nankai University,Tianjin 300071,China 

出  处:《Science China Chemistry》2010年第9期1899-1906,共8页中国科学(化学英文版)

基  金:the National Natural Science Foundation of China;the National Basic Research Program of China (973 Program) (2006CB806106, 2010CB833300);the Ministry of Health (2009ZX09501-017);"111" Project of the Ministry of Education of China (B06005) for financial support

摘  要:Asymmetric hydrovinylation of silyl-protected allylic alcohols catalyzed by nickel complexes of chiral spiro phosphoramidite ligands was developed.A series of homoallylic alcohols with a chiral quaternary center were produced in high yields(up to 97%) and high enantioselectivities(up to 95% ee).The reaction provides an efficient method for preparing bifunctional compounds with a chiral quaternary carbon center.Asymmetric hydrovinylation of silyl-protected allylic alcohols catalyzed by nickel complexes of chiral spiro phosphoramidite ligands was developed.A series of homoallylic alcohols with a chiral quaternary center were produced in high yields(up to 97%) and high enantioselectivities(up to 95% ee).The reaction provides an efficient method for preparing bifunctional compounds with a chiral quaternary carbon center.

关 键 词:asymmetric hydrovinylation CHIRAL SPIRO phosphorus ligands functionalized olefins CHIRAL QUATERNARY CENTER 

分 类 号:O643.32[理学—物理化学]

 

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