1050366-71-6Relevant academic research and scientific papers
Baylis-Hillman acetates in carbocyclic synthesis: A convenient protocol for synthesis of densely substituted indenes
Basavaiah, Deevi,Reddy, Bhavanam Sekhara,Lingam, Harathi
, p. 1994 - 2003 (2013)
A simple and facile strategy for synthesis of densely substituted indenes have been developed from Baylis-Hillman acetates in a two step protocol, that is, (1) via treatment with DABCO and then reaction with alkyl 3-oxobutanoates in the presence of K2CO3 (2) followed by the intramolecular Friedel-Crafts cyclization of the resulting keto-diesters using titanium tetrachloride.
P2O5-promoted efficient and diastereoselective synthesis of substituted 5-methylene-dihydropyran-2,6-diones and 3-methylene-3,4-dihydropyran-2-ones
Singh, Vijay,Madapa, Sudharshan,Batra, Sanjay
, p. 2113 - 2124 (2008/09/21)
A simple, efficient, and diastereoselective synthesis of 5-methylene-dihydropyran-2,6-diones and 3-methylene-3,4-dihydropyran-2-ones from substrates afforded by the SN2 reaction between the acetyl derivatives of the Baylis-Hillman adducts and methylacetoa
