Discovery of 126456-43-7

But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! Read on for other articles about 120-93-4!, 126456-43-7

An article , which mentions 126456-43-7, molecular formula is C9H11NO. The compound – (1S,2R)-1-Amino-2,3-dihydro-1H-inden-2-ol played an important role in people’s production and life., 126456-43-7

Oxazoline-substituted prolinamide-based organocatalysts for the direct intermolecular aldol reaction between cyclohexanone and aromatic aldehydes

Oxazoline-substituted prolinamides catalyse the direct asymmetric aldol reaction between cyclohexanone and a range of aldehydes to give excellent conversions and enantioselectivities up to 84% under optimum conditions. Reactions were highly substrate-specific with electron-deficient aldehydes giving the highest yields and ee values. The absolute configuration of the 4-chlorobenzaldehyde-derived product was unequivocally established as (2S,1?R) by single-crystal X-ray analysis, and the stereochemistry of the product was shown to be determined principally by the stereochemistry of the proline fragment. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! Read on for other articles about 120-93-4!, 126456-43-7

Reference£º
Chiral nitrogen ligands in late transition metal-catalysed asymmetric synthesis¡ªI. Addressing the problem of ligand lability in rhodium-catalysed hydrosilations,
Nitrogen-Containing Ligands for Asymmetric Homogeneous and Heterogeneous Catalysis