Recoverable chiral sulfoxides for asymmetric synthesis: application to stereoselective carbonyl reduction and the asymmetric synthesis of allylic alcohols

Author(s):  
Roger J. Butlin ◽  
Ian D. Linney ◽  
Mary F. Mahon ◽  
Heather Tye ◽  
Martin Wills
1994 ◽  
Vol 35 (29) ◽  
pp. 5297-5300 ◽  
Author(s):  
Guy Solladié ◽  
Nathalie Huser ◽  
José Luis Garcia-Ruano ◽  
Javier Adrio ◽  
M.Carmen Carreño ◽  
...  

2008 ◽  
Vol 75 (2) ◽  
pp. 551-556 ◽  
Author(s):  
Ai-Tao Li ◽  
Jian-Dong Zhang ◽  
Jian-He Xu ◽  
Wen-Ya Lu ◽  
Guo-Qiang Lin

ABSTRACT A new and efficient sulfide monooxygenase-producing strain, ECU0066, was isolated and identified as a Rhodococcus sp. that could transform phenylmethyl sulfide (PMS) to (S)-sulfoxide with 99% enantiomeric excess via two steps of enantioselective oxidations. Its enzyme activity could be effectively induced by adding PMS or phenylmethyl sulfoxide (PMSO) directly to a rich medium at the early log phase (6 h) of fermentation, resulting in over 10-times-higher production of the enzyme. This bacterial strain also displayed fairly good activity and enantioselectivity toward seven other sulfides, indicating a good potential for practical application in asymmetric synthesis of chiral sulfoxides.


ChemInform ◽  
2010 ◽  
Vol 25 (34) ◽  
pp. no-no
Author(s):  
I. D. LINNEY ◽  
H. TYE ◽  
M. WILLS ◽  
R. J. BUTLIN

2018 ◽  
Vol 455 ◽  
pp. 78-87 ◽  
Author(s):  
Chenyue Li ◽  
Changxuan Ke ◽  
Ruirui Han ◽  
Guoli Fan ◽  
Lan Yang ◽  
...  

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