1619923-81-7Relevant articles and documents
Proline-catalyzed asymmetric Diels-Alder reactions of an o-quinodimethane
Shirakawa, Hidenori,Sano, Hiroshi
, p. 4095 - 4097 (2014/07/22)
Catalytic asymmetric Diels-Alder reaction of α-amino-o-quinodimethane with α,β-unsaturated aldehydes was achieved with high diastereo- and enantioselectivities in the presence of l-proline, which acts as a promoter to generate the quinodimethane from the corresponding precursor as well as a chiral catalyst for the enantioselective Diels-Alder reaction.