An Efficient Route to Chiral α- and β-Hydroxyalkanephosphonates
作者:Oscar Pàmies、Jan-E. Bäckvall
DOI:10.1021/jo026888m
日期:2003.6.1
Enzymatic kinetic resolution of alpha- and beta-hydroxyphosphonates in combination with ruthenium-catalyzed alcohol isomerization led to a successful dynamic kinetic resolution. A variety of racemic hydroxyphosphonates were efficiently transformed to the corresponding enantiomerically pure acetates (ee up to 99% and yield up to 87%).
Biocatalytic separation of α-hydroxyphosphonates with lipase of Burkholderia cepacia
作者:O. O. Kolodyazhnaya、O. I. Kolodyazhnyi
DOI:10.1134/s1070363210080244
日期:2010.8
Nonenzymatic kinetic resolution of racemic α-hydroxyalkanephosphonates with chiral copper catalyst
作者:Yosuke Demizu、Atsushi Moriyama、Osamu Onomura
DOI:10.1016/j.tetlet.2009.07.003
日期:2009.9
Kinetic resolution of alpha-hydroxyalkanephosphonates was efficiently performed by benzoylation in the presence of copper(II) triflate and (R,R)-Ph-BOX as a catalyst with excellent s value of up to 286. (C) 2009 Elsevier Ltd. All rights reserved.