Issue 5, 1984
From the journal:

Journal of the Chemical Society, Chemical Communications

β-Hydroxydecanoylthioester dehydraes. Steric course at substrate C–4 in the enzyme–catalysed allylic rearrangement

John M. Schwab  and  John B. Klassen  

Abstract

The pro-(4R)hydrogen is lost in the enzyme-catalysed rearrangement of the N-acetylcysteinamine thioseter of E-dec-2-enoic acid to the corresponding thioester of Z-dec-3-enoic acid.

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Article information

DOI
https://doi.org/10.1039/C39840000296
Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 296-297

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β-Hydroxydecanoylthioester dehydraes. Steric course at substrate C–4 in the enzyme–catalysed allylic rearrangement

J. M. Schwab and J. B. Klassen, J. Chem. Soc., Chem. Commun., 1984, 296 DOI: 10.1039/C39840000296

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