1195790-88-5Relevant articles and documents
Asymmetric organocatalytic double-conjugate addition of malononitrile to dienones: Efficient synthesis of optically active cyclohexanones
Li, Xue-Ming,Wang, Bo,Zhang, Jun-Min,Yan, Ming
supporting information; experimental part, p. 374 - 377 (2011/04/15)
9-Amino-9-deoxyepiquinine efficiently catalyzed the double-conjugate addition of malononitrile to dienones. A number of 1,1,2,6-tetrasubstituted cyclohexanones were prepared in good yields, diastereoselectivities, and excellent enantioselectivities.
Double cascade reactions based on the Barbas dienamine platform: Highly stereoselective synthesis of functionalized cyclohexanes for cardiovascular agents
Ramachary, Dhevalapally B.,Reddy, Y. Vijayendar,Prakash, B. Veda
, p. XX719-726 (2008/09/16)
The amino acid proline catalyzed the three- and five-component cascade olefination-Diels-Alder-epimerization and olefination-Diels-Alder-epimerization- olefination-hydrogenation reactions of readily available precursors enones 1a-i, arylaldehydes 2a-k, al
