173547-32-5Relevant academic research and scientific papers
Asymmetric multifunctional organocatalytic Michael addition of nitroalkanes to α,β-unsaturated ketones
Li, Pengfei,Wang, Yongcan,Liang, Xinmiao,Ye, Jinxing
supporting information; experimental part, p. 3302 - 3304 (2009/02/04)
Cinchona alkaloid derived primary amine thioureas organocatalyzed Michael addition of nitroalkanes to enones in good yield and up to 98% ee and offered a new way to construct quaternary stereocenters from enones and nitroalkanes. The Royal Society of Chem
Asymmetric conjugate addition of nitroalkanes to enones with a chiral α-aminophosphonate catalyst
Malmgren, Marcus,Granander, Johan,Amedjkouh, Mohamed
, p. 1934 - 1940 (2008/12/22)
Chiral diethyl (2R)-tetrahydropyrro-2-ylphosphonate is an effective catalyst for the Michael addition of nitroalkanes to α,β-unsaturated ketones. This study revealed that the hydrate salt of this α-aminophosphonate was found to be a better catalytic speci
Clemmensen Reduction. XI. Fragmentation Reactions of Some 3-Acetylcycloalkanones
Bailey, Karen E.,Davis, Brian R.
, p. 1827 - 1834 (2007/10/03)
Clemmensen reduction of a series of 3-acetylcycloalkanones yields, as the major product, an acyclic unsaturated ketone, the product of fragmentation.Some normal carbonyl-methylene reduction also occurs.A mechanistic rationale for the fragmentation is advanced.
