164334-44-5Relevant academic research and scientific papers
Highly Stereocontrolled Sequential Asymmetric Michael Addition Reactions with Cinnamate Esters - Generation of Three and Four Contiguous Stereogenic Centers on Seven-Carbon Acyclic Motifs
Hanessian, Stephen,Gomtsiyan, Arthur
, p. 7509 - 7512 (1994)
The reaction of allyl and crotyl bicyclic chiral phosphonamide anions with two cinnamate esters leads to a sequential Michael reaction with excellent diastereoselectivity.The option to quench enolates with methyl iodide greatly enhances the versatility of
