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MgBr2-promoted enantioselective aryl addition of ArTi(OiPr)3 to ketones catalyzed by a titanium(iv) catalyst of N,N′-sulfonylated (1R,2R)-cyclohexane-1,2-diamine†
Chao-Chi Shu,Shuangliu Zhou,Han-Mou Gau
RSC Advances Pub Date : 11/10/2015 00:00:00 , DOI:10.1039/C5RA18871G
Abstract

MgBr2-promoted asymmetric addition of ArTi(OiPr)3 to ketones catalyzed by a titanium catalyst of N,N′-sulfonylated (1R,2R)-cyclohexane-1,2-diamines is reported, and results showed that the chiral N,N′-sulfonylated cyclohexane-1,2-diamines with electron-withdrawing groups could effectively catalyze asymmetric addition of ArTi(OiPr)3 to ketones to afford desired tertiary alcohols in good yields with good to excellent enantioselectivities of up to 95% ee.

Graphical abstract: MgBr2-promoted enantioselective aryl addition of ArTi(OiPr)3 to ketones catalyzed by a titanium(iv) catalyst of N,N′-sulfonylated (1R,2R)-cyclohexane-1,2-diamine
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