On the specificity of reactions catalysed by the antibody H11

Tools

Khalaf, Abedawn I. and Linaza, Sabin and Pitt, Andrew R. and Stimson, William H. and Suckling, Colin J. (2000) On the specificity of reactions catalysed by the antibody H11. Tetrahedron, 56 (3). pp. 489-495. ISSN 0040-4020 (https://doi.org/10.1016/S0040-4020(99)01037-6)

Full text not available in this repository.Request a copy

Abstract

The substrate specificity and the stereochem. course of the reactions catalyzed by the antibody H11 (which was raised to a protein conjugated deriv. of the adduct of 1-acetoxy-buta-1,3-diene 1) have been investigated. The antibody shows high selectivity for acetoxybutadiene which it hydrolyzes to the corresponding dienol, the major diene component of the cycloaddn. reactions obsd. However, it tolerates a range of N-alkylmaleimides. The stereochem. course of cycloaddn. is shown to produce a significant enantiomeric excess of the 3aR,4S,7aR-endo-diastereoisomer by anal. with Mosher's ester derivs. This study also revealed that H11 is capable of slowly catalyzing the hydrolysis of N-alkylmaleimide substrates. The implications for the mechanism of action of H11 are discussed. [on SciFinder(R)]

ORCID iDs

Khalaf, Abedawn I. ORCID logoORCID: https://orcid.org/0000-0001-9162-7527, Linaza, Sabin, Pitt, Andrew R., Stimson, William H. and Suckling, Colin J.;
  • Item type:Article
    ID code:712
    Dates:
    Date
    Event
    14 January 2000
    Published
    Notes:M1 - Copyright (C) 2011 American Chemical Society (ACS). All Rights Reserved. CAPLUS AN 2000:97446(Journal)
    Subjects:Science > Chemistry
    Department:Faculty of Science > Pure and Applied Chemistry
    Depositing user: Strathprints Administrator
    Date deposited:02 May 2006
    Last modified:11 Nov 2024 08:15
    URI:https://strathprints.strath.ac.uk/id/eprint/712
CORE (COnnecting REpositories)