Mechanism of Site-Directed Protein Cross-Linking. Protein-Directed Selectivity in Reactions of Hemoglobin with Aryl Trimesates
Author:
Affiliation:
1. Lash Miller Laboratories, Department of Chemistry, University of Toronto, Toronto, Ontario, Canada M5S 3H6
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo991514n
Reference21 articles.
1. Kluger, R.Chemical cross-linking and protein function; Creighton, T. E., Ed.; IRL Press: Oxford, U.K., 1997; pp 185−214.
2. Trimesoyltris(3,5-dibromosalicylate): specificity of reactions of a trifunctional acylating agent with hemoglobin
3. Bornadiene thermolysis. A new entry into the trimethyltropilidene labyrinth
4. Changing a protein into a generalized acylating reagent. Reaction of nucleophiles with 3,5-dibromosalicyl trimesyl-((Lys-.beta.-82)-(Lys-.beta.-82))-hemoglobin
5. Alternative aspirins as antisickling agents: acetyl-3,5-dibromosalicylic acid.
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