Chemoenzymatic enantioselective synthesis of baclofen
1994 ◽
Vol 72
(11)
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pp. 2312-2317
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Keyword(s):
We report two different chemoenzymatic enantioselective syntheses of baclofen based on the distinction between enantiotopic ester groups in compounds bearing a prochiral centre. In the first approach, the key step is the highly stereoselective enzymatic hydrolysis of dimethyl 3-(4-chlorophenyl)glutarate by chymotrypsin in an aqueous medium. In the second approach, the key step is the enzyme-catalyzed esterification of 2-(4-chloropheny 1)-1,3-propanediol by acetic anhydride in the presence of a lipase in an organic medium.
1993 ◽
Vol 41
(9)
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pp. 1521-1523
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1974 ◽
Vol 76
(1)
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pp. 7-13
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Keyword(s):
2010 ◽
Vol 160-162
◽
pp. 1358-1361
Keyword(s):
2018 ◽
Vol 15
(2)
◽
pp. 221-229
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2019 ◽
Vol 15
(3)
◽
pp. 296-303
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