Practical synthesis and biological screening of sulfonyl hydrazides

Author:

Macara João1,Caldeira Catarina1,Cunha José1ORCID,Coelho Jaime A. S.2ORCID,Silva Maria J. S. A.3ORCID,Krämer Konrad45,Grathwol Christoph W.45,Bräse Stefan45,Marques M. Manuel B.1ORCID

Affiliation:

1. LAQV@REQUIMTE, Departamento de Química, NOVA School of Science and Technology, Universidade Nova de Lisboa, Campus de Caparica, 2829-516 Caparica, Portugal

2. Centro de Química Estrutural, Faculdade de Ciências, Universidade de Lisboa, Campo Grande, Lisboa 1749-016, Portugal

3. Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Av. Prof. Gama Pinto, 1649-003, Lisboa, Portugal

4. Institute of Organic Chemistry, Organic Chemistry I, Fritz-Haber-Weg 6, 76131 Karlsruhe, Germany

5. Institute of Biological and Chemical Systems – Functional Molecular Systems (IBCS-FMS), Hermann-von-Helmholtz-Platz 1, D-76344 Eggenstein-Leopoldshafen, Germany

Abstract

A hypervalent iodine-mediated synthesis of sulfonyl hydrazides is described. The methodology relies on the umpolung reactivity of benziodoxolone reagents. Mechanistic studies and biological screening were performed.

Funder

Fundação para a Ciência e a Tecnologia

Laboratório Associado para a Química Verde

European Regional Development Fund

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

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