591250-21-4Relevant articles and documents
Synthesis of 2-amino-3,4-dihydroquinazolines and imidazo[2,1-b]quinazoline- 2-ones
Mishra, Amita,Batra, Sanjay
scheme or table, p. 3077 - 3088 (2009/12/28)
A straightforward method for the synthesis of 2-amino-3,4- dihydroquinazolines from Baylis-Hillman derivatives is disclosed. The protocol involves sequential SN2 reaction of a primary amine on the Baylis-Hillman acetate derived from 2-nitrobenzaldehyde, c
Synthesis of substituted 3-methylene-2-pyridones from Baylis-Hillman derivatives and its application for the generation of 2-pyridone substituted spiroisoxazolines
Singh, Virender,Yadav, Gaya P.,Maulik, Prakas R.,Batra, Sanjay
, p. 2979 - 2991 (2008/09/19)
The synthesis of substituted 3-methylene-2-pyridones via SN2 displacement reaction of nucleophiles bearing a keto group on the acetyl derivative of Baylis-Hillman adducts of acrylonitrile followed by TFA/H2SO4-mediated int
Synthesis of 3-substituted quinolines via transition-metal-catalyzed reductive cyclization of o-nitro baylis-hillman acetates
O'Dell, David K.,Nicholas, Kenneth M.
, p. 6427 - 6430 (2007/10/03)
Reductive cyclization of o-nitro-substituted Baylis-Hillman acetates by carbon monoxide, catalyzed by [Cp*Fe(CO)2]2, gives moderate to good yields of 3-substituted quinolines.
