A Route to Bis(benzimidazole) Ligands with Built-In Asymmetry: Potential Models of Protein Binding Sites Having Histidines of Different Basicity-Reference-Cited by-同舟云学术

A Route to Bis(benzimidazole) Ligands with Built-In Asymmetry: Potential Models of Protein Binding Sites Having Histidines of Different Basicity

Published:1996-01-01 Issue:26 Volume:35 Page:7563-7571
ISSN:0020-1669
Container-title:Inorganic Chemistry
language:en
Short-container-title:Inorg. Chem.

Author:

Matthews Craig J.¹,Leese Troy A.¹,Clegg William¹,Elsegood Mark R. J.¹,Horsburgh Lynne¹,Lockhart Joyce C.¹

Affiliation:

1. Department of Chemistry, University of Newcastle Upon Tyne, Newcastle Upon Tyne NE1 7RU, U.K., and Zeneca Specialties, PO Box 42, Hexagon House, Blackley, Manchester M9 8ZS, U.K.

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ic960777m

Reference37 articles.

1. Bifunctional acid—base catalysis by imidazole groups in enzyme mimics

2. Use of Ligand Design to Provide Coordination Asymmetry in a Binuclear Metalloprotein Model System: Ligand Synthesis, Coordination Chemistry with Copper, and Demonstration of Site-Directed Reactivity

3. Synthesis and crystal structures of some bis-benzimidazoles, -benzothiazoles and -benzoxazoles by an alternative route: their complexation with copper(II) salts

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