74046-14-3Relevant academic research and scientific papers
Synthesis and application of peripherally alkyl-functionalized dendritic pyrphos ligands: Homogeneous-supported catalysts for enantioselective hydrogenation
Yi, Bing,He, Hua-Ping,Fan, Qing-Hua
experimental part, p. 82 - 85 (2010/04/25)
A new series of dendritic ligands with a chiral diphosphine located at the focal point have been synthesized through coupling of (R,R)-3,4-bis(biphenylphosphino)pyrrolidine (pyrphos) with peripherally alkyl-functionalized benzoic acid dendrons. These ligands were employed in the Rh-catalyzed asymmetric hydrogenation of prochiral dehydroamino acids, exhibiting excellent catalytic activities and enantioselectivities. The second-generation dendritic catalyst could be recovered by simple liquid-liquid biphasic separation and reused four times without serious loss of its activity and selectivity.
Novel atropisomeric bisphosphine ligands with a bridge across the 5,5′-position of the biphenyl for asymmetric catalysis
Wei, Hao,Zhang, Yong Jian,Wang, Feijun,Zhang, Wanbin
, p. 482 - 488 (2008/09/19)
A new type of atropisomeric bisphosphine ligand 2 with a bridge across the 5,5′-position of the biphenyl has been developed. The axial chirality of this type of ligands can be retained by macrocyclic ring strain produced from 5,5′-linkage of the biphenyl
Synthesis of a novel spiro bisphosphinite ligand and its application in Rh-catalyzed asymmetric hydrogenation
Guo, Zhenqiu,Guan, Xiaoyu,Chen, Zhiyong
, p. 468 - 473 (2007/10/03)
A novel, chiral bisphosphinite ligand (R)-SpiroBIP has been synthesized. The rhodium complex of the ligand was found to be highly enantioselective in the asymmetric hydrogenation of α-dehydroamino acid derivatives.
H8-MonoPhos and its application in catalytic enantioselective hydrogenation of α-dehydroamino acids
Zeng, Qingle,Liu, Hui,Mi, Aiqiao,Jiang, Yaozhong,Li, Xingshu,Choi, Michael C.K,Chan, Albert S.C
, p. 8799 - 8803 (2007/10/03)
H8-MonoPhos, a new stable and readily soluble monodentate phosphoramidite ligand, has been facilely prepared from H8-BINOL. The ligand achieved up to 99.9% ee and 96.7% ee in hydrogenation of dehydroalanine and dehydrohomophenylalani
Acylase I catalysed hydrolysis of para-substituted (S)-phenylalanine derivatives from mixtures of the racemic ortho- and para-substituted isomers
Easton, Christopher J.,Harper, Jason B.
, p. 5269 - 5272 (2007/10/03)
para-Substituted (S)-phenylalanines may be obtained by treatment of the corresponding mixtures of ortho- and para-substituted N-acetyl-(RS)- phenylalanines with Acylase I from porcine kidney. The selectivity of the enzyme may be attributed to its evolution to digest peptide derivatives of (S)-phenylalanine and (S)-tyrosine.
