64030-44-0Relevant articles and documents
Chiral azo-heterocyclic carbene precursor compound with bicyclic framework and preparation method thereof
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Paragraph 0082; 0083; 0084; 0085; 0090; 0092; 0093, (2019/01/22)
The invention discloses a chiral azo-heterocyclic carbene precursor compound with a bicyclic framework and a preparation method thereof. A series of the chiral azo-heterocyclic carbene precursor compound with the bicyclic framework is obtained by taking c
Transfer hydrogenation reactions catalyzed by chiral half-sandwich Ruthenium complexes derived from Proline
Pandia Kumar, Arun Kumar,Samuelson, Ashoka G
, p. 1405 - 1415 (2016/09/19)
Chiral ruthenium half-sandwich complexes were prepared using a chelating diamine made from proline with a phenyl, ethyl, or benzyl group, instead of hydrogen on one of the coordinating arms. Three of these complexes were obtained as single diastereoisomers and their configuration identified by X-ray crystallography. The complexes are recyclable catalysts for the reduction of ketones to chiral alcohols in water. A ruthenium hydride species is identified as the active species by NMR spectroscopy and isotopic labelling experiments. Maximum enantio-selectivity was attained when a phenyl group was directly attached to the primary amine on the diamine ligand derived from proline. [Figure not available: see fulltext.]
Chiral amine catalyzed enantio- and diastereoselective Michael reaction in brine
Singh, Sarbjit,Chimni, Swapandeep Singh
, p. 1068 - 1079 (2012/11/06)
Simple pyrrolidine-based chiral amines were synthesized and used for the Michael addition of different ketones to a variety of nitro-olefins in brine. The effect of different surfactants and acids on the yields and stereochemical outcome of the Michael ad
