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- W2071284207 endingPage "184" @default.
- W2071284207 startingPage "175" @default.
- W2071284207 abstract "Abstract The hydrolysis of a series of norbornane‐type carboxylic esters catalyzed by pig liver esterase (PLE) has been investigated. It was found that an exo ‐eer function ( syn to the C7 methylene group) is hydrolyzed with high preference. Enantioselective hydrolysis can be accomplished when a vicinal carbonyl‐containing function (eer, formyl, acetyl) is present in a trans position with respect to the exo eer. The regiospecificity of the enzymatic hydrolysis has been used for the separation of exo/endo mixtures of the cycloadducts derived from cyclopentadiene and alkene esters. The regiospecificity and enantioselectivity of the enzymatic hydrolysis of norbornane‐type esters were analyzed in terms of Tamm's substrate model and also by Griengl's method." @default.
- W2071284207 created "2016-06-24" @default.
- W2071284207 creator A5050333335 @default.
- W2071284207 creator A5054865401 @default.
- W2071284207 creator A5073179210 @default.
- W2071284207 date "1991-01-01" @default.
- W2071284207 modified "2023-10-09" @default.
- W2071284207 title "Enzymatic optical resolution of norbornanecarboxylic esters using pig liver esterase" @default.
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- W2071284207 doi "https://doi.org/10.1002/recl.19911100508" @default.
- W2071284207 hasPublicationYear "1991" @default.
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