Diverse structural assemblies of U-shaped hydrazinyl-sulfonamides: experimental and theoretical analysis of non-covalent interactions stabilizing solid state conformations-Reference-Cited by-同舟云学术

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Diverse structural assemblies of U-shaped hydrazinyl-sulfonamides: experimental and theoretical analysis of non-covalent interactions stabilizing solid state conformations

Published:2019 Issue:11 Volume:21 Page:1780-1793
ISSN:1466-8033
Container-title:CrystEngComm
language:en
Short-container-title:CrystEngComm

Author:

Andleeb Hina¹²³⁴,Khan Imtiaz¹²³⁴⁵^ORCID,Franconetti Antonio⁶⁷⁸⁹^ORCID,Tahir Muhammad Nawaz¹⁰¹¹¹²⁴,Simpson Jim¹¹³¹⁴¹⁵^ORCID,Hameed Shahid¹²³⁴^ORCID,Frontera Antonio⁶⁷⁸⁹^ORCID

Affiliation:

1. Department of Chemistry

2. Quaid-i-Azam University

3. Islamabad-45320

4. Pakistan

5. School of Chemistry & Manchester Institute of Biotechnology

6. Departament de Química

7. Universitat de les Illes Balears

8. 07122 Palma de Mallorca (Baleares)

9. Spain

10. Department of Physics

11. University of Sargodha

12. Sargodha

13. University of Otago

14. Dunedin

15. New Zealand

Abstract

The preparation and structures of five new U-shaped hydrazinyl-sulfonamides are reported.

Funder

Higher Education Commision, Pakistan

University of Otago

Secretaría de Estado de Investigación, Desarrollo e Innovación

Publisher

Royal Society of Chemistry (RSC)

Subject

Condensed Matter Physics,General Materials Science,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/CE/C8CE01917G

Reference105 articles.

1. Divergent C–H Functionalizations Directed by Sulfonamide Pharmacophores: Late-Stage Diversification as a Tool for Drug Discovery

2. Synthesis, Antioxidant, and Antiacetylcholinesterase Activities of Sulfonamide Derivatives of Dopamine-Related Compounds

3. Novel biphenyl bis -sulfonamides as acetyl and butyrylcholinesterase inhibitors: Synthesis, biological evaluation and molecular modeling studies

4. Carbonic anhydrases: novel therapeutic applications for inhibitors and activators

5. Multiple Binding Modes of Inhibitors to Carbonic Anhydrases: How to Design Specific Drugs Targeting 15 Different Isoforms?

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