Enzymatic Desymmetrization of Dimethyl Cylcohex-4-ene-cis-1,2-dicarboxylate to (1S,2R)-2-(Methoxycarbonyl)cyclohex-4-ene-1-carboxylic Acid
Author:
Affiliation:
1. Process Research and Development, Bristol-Myers Squibb, New Brunswick, New Jersey 08903, U.S.A.
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/op8002954
Reference24 articles.
1. aCherney, R. J.; Carter, P.; Duncia, J. V.; Gardner, D. S.; Santella, J. B.PCT Int. Appl. WO/2004/071460 A2, 2004.
2. bCarter, P. H.; Cherney, R. J.; Batt, D. G.; Duncia, J. V.; Gardner, D. S.; Ko, S.; Srivastava, A. S.; Yang, M. G.PCT Int. Appl.WO/2005/021500 A1, 2005.
3. An efficient synthesis of a key intermediate for optically active 5,6--carbapenem antibiotics
4. Enzym-katalysierte asymmetrische Synthese, IV. Synthese homochiraler Bausteine für die enantioselektive Totalsynthese von Cyclopentanoiden mit Esterase-katalysierter asymmetrischer Schlüsselreaktion
5. Synthesis of carbapenems with a sulfonyl group in the C-6 side-chain and their biological activity.
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