Inside Cover: Organocatalytic Enantioselective Morita–Baylis–Hillman Reaction of Maleimides with Isatins (Asian J. Org. Chem. 7/2013)
Inside Cover: Organocatalytic Enantioselective Morita–Baylis–Hillman Reaction of Maleimides with...
Chauhan, Pankaj; Chimni, Swapandeep Singh
2013-07-01 00:00:00
Organocatalysis Maleimides are known to be very good electrophiles, dienophiles, and dipolarophiles. In their Full Paper on page 586 ff., Pankaj Chauhan and Swapandeep Singh Chimni demonstrate that maleimide derivatives can be used as nucleophilic partners in an efficient organocatalytic Morita‐Baylis‐Hillman reaction with isatins catalyzed by β‐isocupreidine. This reaction gives chiral 3‐substituted‐3‐hydroxyoxindoles in high yield and excellent enantioselectivity.
http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.pngAsian Journal of Organic ChemistryWileyhttp://www.deepdyve.com/lp/wiley/inside-cover-organocatalytic-enantioselective-morita-baylis-hillman-sZ0Jy1pRdA
Inside Cover: Organocatalytic Enantioselective Morita–Baylis–Hillman Reaction of Maleimides with Isatins (Asian J. Org. Chem. 7/2013)
Organocatalysis Maleimides are known to be very good electrophiles, dienophiles, and dipolarophiles. In their Full Paper on page 586 ff., Pankaj Chauhan and Swapandeep Singh Chimni demonstrate that maleimide derivatives can be used as nucleophilic partners in an efficient organocatalytic Morita‐Baylis‐Hillman reaction with isatins catalyzed by β‐isocupreidine. This reaction gives chiral 3‐substituted‐3‐hydroxyoxindoles in high yield and excellent enantioselectivity.
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