1169855-38-2Relevant academic research and scientific papers
1,3-dipolar cycloaddition on baylis-hillman adducts: Novel synthesis of pyrrolidines, spiropyrrolidines, and spiropyrrolizidines
Bakthadoss, Manickam,Sivakumar, Nagappan,Devaraj, Anthonisamy,Sharada, Duddu S.
experimental part, p. 2136 - 2146 (2011/08/05)
A facile regio- and stereoselective synthesis of functionalized pyrrolidines, spiropyrrolidines, and spiropyrrolizidines using the Baylis-Hillman adducts derived from nitroolefins via intermolecular [3+2]-cycloaddition reaction is reported. Georg Thieme Verlag Stuttgart ? New York.
First synthesis of bromo and chloro derivatives of baylis-hillman adducts derived from nitroolefins: Application towards the synthesis of a dendrimer core
Bakthadoss, Manickam,Sivakumar, Nagappan,Devaraj, Anthonisamy
experimental part, p. 611 - 618 (2011/04/15)
For the first time Baylis-Hillman adducts derived from nitroolefins have been conveniently transformed into a novel class of building blocks, 1-[(E)-3-bromo-2-nitroprop-1-enyl]arenes and 1-[(E)-3-chloro-2-nitroprop-1-enyl] arenes, in very good yields via
