Enzyme-mediated asymmetric hydrolysis of α-benzyloxycarboxylic esters
Y Kato, H Ohta, G Tsuchihashi
Index: Kato, Yasuo; Ohta, Hiromichi; Tsuchihashi, Gen-ichi Tetrahedron Letters, 1987 , vol. 28, # 12 p. 1303 - 1306
Full Text: HTML
Citation Number: 23
Abstract
Abstract Incubation of d1-α-benzyloxycarboxylic esters with grown cells of a bacterium, Corynebacterium equi IFO 3730, afforded the chiral esters of high optical purities via asymmetric hydrolysis. This reaction has been revealed to have a wide applicability to alkane-and arylalkane-carboxylic esters.
Related Articles:
[Ley, Steven V.; Diez, Elena; Dixon, Darren J.; Guy, Richard T.; Michel, Patrick; Nattrass, Gillian L.; Sheppard, Tom D. Organic and Biomolecular Chemistry, 2004 , vol. 2, # 24 p. 3608 - 3617]
Process research of (R)-cyclohexyl lactic acid and related building blocks: a comparative study
[Storz, Thomas; Dittmar, Peter; Fauquex, Pierre Francois; Marschal, Philippe; Lottenbach, Willy Urs; Steiner, Heinz Organic Process Research and Development, 2003 , vol. 7, # 4 p. 559 - 570]
[Yamano, Toru; Kikumoto, Fumio; Yamamoto, Shozo; Miwa, Katsuhiko; Kawada, Mitsuru; Ito, Tatsuya; Ikemoto, Tomomi; Tomimatsu, Kiminori; Mizuno, Yukio Chemistry Letters, 2000 , # 5 p. 448 - 449]
Stereoselective hetero-Claisen rearrangement of camphor derived oxazoline-N-oxides
[Dalko, Peter I.; Langlois, Yves Tetrahedron Letters, 1998 , vol. 39, # 15 p. 2107 - 2110]
Stereoselective hetero-Claisen rearrangement of camphor derived oxazoline-N-oxides
[Dalko, Peter I.; Langlois, Yves Tetrahedron Letters, 1998 , vol. 39, # 15 p. 2107 - 2110]