N-Alkylation and Aminohydroxylation of 2-Azidobenzenesulfonamide Gives a Pyrrolobenzothiadiazepine Precursor Whereas Attempted N-Alkylation of 2-Azidobenzamide Gives Benzotriazinones and Quinazolinones-Reference-Cited by-同舟云学术

N-Alkylation and Aminohydroxylation of 2-Azidobenzenesulfonamide Gives a Pyrrolobenzothiadiazepine Precursor Whereas Attempted N-Alkylation of 2-Azidobenzamide Gives Benzotriazinones and Quinazolinones

Published:2017-03-31 Issue:3 Volume:2 Page:1222-1231
ISSN:2470-1343
Container-title:ACS Omega
language:en
Short-container-title:ACS Omega

Author:

Hamasharif Muslih S.¹,Smith Oliver E. P.¹,Curran Collette J.¹,Hemming Karl¹^ORCID

Affiliation:

1. Department of Chemistry, University of Huddersfield, Queensgate, Huddersfield, West Yorkshire HD1 3DH, United Kingdom

Funder

University of Huddersfield

Kurdistan Regional Government

Publisher

American Chemical Society (ACS)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.acs.org/doi/pdf/10.1021/acsomega.7b00211

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4. Effect of hairpin loop structure on reactivity, sequence preference and adduct orientation of a DNA-interactive pyrrolo[2,1-c][1,4]benzodiazepine (PBD) antitumour agent

5. Pyrrolobenzodiazepines (PBDs) Do Not Bind to DNA G-Quadruplexes

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