130146-97-3Relevant academic research and scientific papers
Inverse electron demand Diels-Alder reactions of N-sulfonyl α,β-unsaturated imines: A general approach to implementation of the 4π participation of 1-aza-1,3-butadienes in Diels-Alder reactions
Boger, Dale L.,Corbett, Wendy L.,Curran, Timothy T.,Kasper
, p. 1713 - 1729 (2007/10/02)
Full details of a study of the inverse electron demand Diels-Alder reactions of W-sulfonyl-1 -aza-1,3-tmtadienes are described. The α,β-unsaturated N-sulfonylimines proved accessible through clean, homolytic rearrangement of in situ generated oxime O-sulf
Diels-Alder Reactions of 1-Aza-1,3-butadienes: Room Temperature, Endo-Selective LUMOdiene-Controlled Cycloaddition Reactions of N-Sulfonyl-4-(ethoxycarbonyl)-1-aza-1,3-butadiene
Boger, Dale L.,Curran, Timothy T.
, p. 5439 - 5442 (2007/10/02)
The room temperature, endo-selective LUMOdiene-controlled Diels-Alder reactions of N-(phenylsulfonyl)- and N-(methylsulfonyl)-4-(ethoxycarbonyl)-1-aza-1,3-butadiene (3-4) are described, and the results represent a demonstration of the cyc
