An intramolecular 1,5-chalcogen bond on the conformational preference of carbonyl thiocarbamate species-Reference-Cited by-同舟云学术

An intramolecular 1,5-chalcogen bond on the conformational preference of carbonyl thiocarbamate species

Published:2020 Issue:14 Volume:44 Page:5243-5253
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Channar Pervaiz Ali¹²³⁴^ORCID,Saeed Aamer¹²³⁴^ORCID,Larik Fayaz Ali¹²³⁴^ORCID,Flörke Ulrich⁵⁶⁷⁸⁹,El-Seedi Hesham¹⁰¹¹¹²¹³¹⁴^ORCID,Rodríguez Pirani Lucas S.¹⁵¹⁶¹⁷¹⁸¹⁹,Erben Mauricio F.¹⁵¹⁶¹⁷¹⁸¹⁹^ORCID

Affiliation:

1. Department of Chemistry

2. Quaid-I-Azam University

3. Islamabad 45320

4. Pakistan

5. Department Chemie

6. Fakultät für Naturwissenschaften

7. Universität Paderborn

8. D-33098 Paderborn

9. Germany

10. International Research Center for Food Nutrition and Safety

11. Jiangsu University

12. Zhenjiang 212013

13. China

14. Al-Rayan Research and Innovation Center

15. CEQUINOR (UNLP, CONICET-CCT La Plata)

16. Departamento de Química

17. Facultad de Ciencias Exactas

18. Universidad Nacional de La Plata

19. La Plata

Abstract

Two closely related carbamothioates were prepared by the reaction of benzoyl isothiocyanates and methanol. The crystal structures show the occurrence of 1,5-O⋯O intramolecular short distance that determines the conformational preference.

Funder

Universidad Nacional de La Plata

Fondo para la Investigación Científica y Tecnológica

Consejo Nacional de Investigaciones Científicas y Técnicas

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2020/NJ/C9NJ06417F

Reference52 articles.

1. Synthesis and Antifungal Activities of Alkyl N-(1,2,3-Thiadiazole-4-Carbonyl) Carbamates and S-Alkyl N-(1,2,3-Thiadiazole-4-Carbonyl) Carbamothioates