Enantioselective Synthesis of α-Hydroxy and α-Amino Phosphonates via Catalytic Asymmetric Hydrogenation
摘要:
[GRAPHICS]Cationic rhodium catalysts of the C-2 symmetric DuPHOS (1) and BPE (2) ligands have demonstrated the ability to asymmetrically hydrogenate a novel series of enol phosphonates (3) in good to excellent enantiomeric excess under mild conditions. Initial studies toward the catalytic asymmetric hydrogenation of enamido phosphonates (6 and 7) using the DuPHOS-Rh+ catalysts are also reported.
Kinetic resolution of hydroxyalkanephosphonates catalyzed by Candida antarctica lipase B in organic media
作者:Yonghui Zhang、Chengye Yuan、Zuyi Li
DOI:10.1016/s0040-4020(02)00229-6
日期:2002.4
A series of hydroxyalkanephosphonates were studied as substrates for CALB catalyzed acetylation with emphasis on enantioselectivity and chemical structure of substrates. Some hydroxyalkanephosphonates could be resolved successfully to give both (R)- and (S)-isomers with high enantiomeric excess.
Synthesis of an Optically Active Al(salalen) Complex and Its Application to Catalytic Hydrophosphonylation of Aldehydes and Aldimines
作者:Bunnai Saito、Hiromichi Egami、Tsutomu Katsuki
DOI:10.1021/ja0651005
日期:2007.2.1
serve as an efficient catalyst for hydrophosphonylation of aldehydes and aldimines, giving the corresponding alpha-hydroxy and alpha-amino phosphonates with high enantioselectivity, respectively. The scope of the hydrophosphonylation was wide, and both aliphatic and aromatic aldehydes and aldimines were successfully used as substrates for the reaction. The potent catalysis of the complex is attributed to
Kinetic resolution of racemic α-hydroxyphosphonates by asymmetric esterification using achiral carboxylic acids with pivalic anhydride and a chiral acyl-transfer catalyst
作者:Isamu Shiina、Keisuke Ono、Takayoshi Nakahara
DOI:10.1039/c3cc44293d
日期:——
A practical protocol is developed to directly provide chiral alpha-acyloxyphosphonates and alpha-hydroxyphosphonates from (+/-)-alpha-hydroxyphosphonates utilizing the transacylation process to generate the mixed anhydrides from acid components and pivalic anhydride in the presence of organocatalysts (s-value = 33-518).