Radical diazidation of alkenes: Cu/Fe/Mn catalysis and electrochemical support

Ahmed, Nisar ORCID: https://orcid.org/0000-0002-7954-5251, Khatoon, Saira and Shirinfar, Bahareh 2018. Radical diazidation of alkenes: Cu/Fe/Mn catalysis and electrochemical support. ChemElectroChem 5 (9) , pp. 1245-1248. 10.1002/celc.201800160

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Abstract

The synthetic routes for C‐N3 bond formation through a radical mechanism with the use of transition metals provide efficient diazide products, which can be further applied in many transformations to synthesize various valuable nitrogen‐containing compounds of pharmaceutical interest. The reported methods evidence stoichiometric heavy metals and toxic reagents (as N3‐source) and generally exhibit a limited substrate scope. However, the electrochemical diazidations are found to be environmentally friendly and very simple, while also providing a highly efficient way to synthesize 1,2‐diazide derivatives. Moreover, they provide a smart alternative for easy access to 1,2‐diamines, which can be used for future modern syntheses.

Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	Chemistry
Publisher:	Wiley-Blackwell
ISSN:	2196-0216
Date of First Compliant Deposit:	26 March 2018
Date of Acceptance:	7 March 2018
Last Modified:	28 Nov 2024 05:30
URI:	https://orca.cardiff.ac.uk/id/eprint/110234

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