The Hydrogen Bond Environments of 1H-Tetrazole and Tetrazolate Rings: The Structural Basis for Tetrazole–Carboxylic Acid Bioisosterism-Reference-Cited by-同舟云学术

The Hydrogen Bond Environments of 1H-Tetrazole and Tetrazolate Rings: The Structural Basis for Tetrazole–Carboxylic Acid Bioisosterism

Published:2012-02-21 Issue:3 Volume:52 Page:857-866
ISSN:1549-9596
Container-title:Journal of Chemical Information and Modeling
language:en
Short-container-title:J. Chem. Inf. Model.

Author:

Allen Frank H.¹,Groom Colin R.¹,Liebeschuetz John W.¹,Bardwell David A.¹,Olsson Tjelvar S.G.¹,Wood Peter A.¹

Affiliation:

1. Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, United Kingdom

Publisher

American Chemical Society (ACS)

Subject

Library and Information Sciences,Computer Science Applications,General Chemical Engineering,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ci200521k

Reference47 articles.

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3. Isosterism and molecular modification in drug design

4. Use of crystallographic data in searching for isosteric replacements: Composite crystal-field environments of nitro and carbonyl groups

5. RECAPRetrosynthetic Combinatorial Analysis Procedure: A Powerful New Technique for Identifying Privileged Molecular Fragments with Useful Applications in Combinatorial Chemistry

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