1246300-53-7Relevant articles and documents
Utilizing the asymmetric amino-cope rearrangement as a novel approach to enantiomerically enriched 3-substituted aldehydes
Allin, Steven M.,Horro-Pita, Catarina,Essat, Munira,Aspinall, Ian,Shah, Pritom
, p. 2696 - 2711 (2010)
We report the asymmetric amino-Cope rearrangement of some novel 3-amino-1,5-diene substrates to yield enantiomerically enriched 3-alkyl and 3-aryl aldehyde products. We have developed a system that gives excellent and comparable levels of product enantiomeric excess (ee) for both alkyl-and aryl-substituted products. Our results have implications for the control of the mechanistic pathway of the amino-Cope rearrangement and thus its potential utility in asymmetric synthesis.
