179804-03-6Relevant articles and documents
Selectivity in 1,3-Dipolar cycloadditions of β-substituted captodative olefins - An experimental and DFT transition state study
Herrera, Rafael,Mendoza, Jorge A.,Morales, Miguel A.,Mendez, Francisco,Jimenez-Vazquez, Hugo A.,Delgado, Francisco,Tamariz, Joaquin
, p. 2352 - 2364 (2008/02/08)
Captodative olefins 1-acetylvinyl carboxylates substituted with alkyl groups at the β position, 12, strongly modified the regioselectivity of 1,3-dipolar cycloadditions with respect to the behavior observed for their unsubstituted analogs, 1. When the rea
Highly stereoselective palladium-catalyzed coupling reactions of captodative olefins acetylvinyl arenecarboxylates
Villar, Lourdes,Bullock, Joseph P.,Khan, Matheen M.,Nagarajan, Arumugam,Bates, Roderick W.,Bott, Simon G.,Zepeda, Gerardo,Delgado, Francisco,Tamariz, Joaquin
, p. 9 - 17 (2007/10/03)
The palladium-catalyzed reaction of the captodative olefin 3-(p-nitrobenzoyloxy)-3-buten-2-one (1a) with aryl and vinyl halides gave coupled products 4-aryl-and 4-vinyl-3-(p-nitrobenzoyloxy)-3-buten-2-ones, 4 and 6 respectively, with high Z stereoselectio