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Volumn 47, Issue 13, 2008, Pages 2497-2501

Iron-catalyzed enantioselective hydrosilylation of ketones

Author keywords

Alcohols; Asymmetric catalysis; Homogeneous catalysis; Hydrosilylation; Iron

Indexed keywords

BENZENE; CATALYSIS; CATALYSTS; CHEMICAL REACTIONS; ENANTIOSELECTIVITY; HYDROSILYLATION; ORGANIC COMPOUNDS;

EID: 42449118890     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200705624     Document Type: Article
Times cited : (234)

References (57)
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    • Notably, the Fe catalyst presented herein leads to higher enantioselectivities for several substrates compared to previously reported copper catalysts. For example 2-chloroacetophenone resulted in 31%ee; see B. H. Lipshutz, K. Noson, W. Chrisman, J. Am. Chem. Soc. 2001, 123, 12917-12918.
    • Notably, the Fe catalyst presented herein leads to higher enantioselectivities for several substrates compared to previously reported copper catalysts. For example 2-chloroacetophenone resulted in 31%ee; see B. H. Lipshutz, K. Noson, W. Chrisman, J. Am. Chem. Soc. 2001, 123, 12917-12918.
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    • According to GC-MS analysis of the crude reaction mixture 1
    • According to GC-MS analysis of the crude reaction mixture 1,4-reduction is observed.
    • 4-reduction is observed


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