Highly enantioselective formal aza-Diels-Alder reactions with acylhydrazones and Danishefsky's diene promoted by a silicon Lewis acid
Silicon Lewis acid 3 is effective for the promotion of highly enantioselective cycloaddition reactions of acylhydrazones with Danishefsky's diene (formal aza-Diels-Alder reactions). The reactions are conducted at ambient temperature for 15 min, and produc
Lee, Sharon K.,Tambar, Uttam K.,Perl, Nicholas R.,Leighton, James L.
experimental part
p. 4769 - 4774
(2010/08/07)
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