Stereoselective Anti-Markovnikov Geminal Diamination and Dioxygenation of Vinylarenes Mediated by the Bromonium Ion

Balaji, Pandur Venkatesan and Chandrasekaran, Srinivasan (2016) Stereoselective Anti-Markovnikov Geminal Diamination and Dioxygenation of Vinylarenes Mediated by the Bromonium Ion. In: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY (14). pp. 2547-2554.

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Abstract

A straightforward method is reported for the stereoselective anti-Markovnikov geminal diamination and stoichiometric geminal dioxygenation of vinylarenes mediated by a bromonium ion. The role of the substituent on the nucleophile and the nucleophilicity of the heteroatom in the competing geminal and vicinal addition pathways has been described. The stereoselectivity of the geminal dioxygenation is dependent on the ring size of the product and the position of the substituent that induces the stereoselectivity. The migration of the phenyl group through a semi-pinacol rearrangement during the geminal addition process was confirmed by the results of deuterium labelling studies.

Item Type:	Journal Article
Publication:	EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Publisher:	WILEY-V C H VERLAG GMBH
Additional Information:	Copy right for this article belongs to the WILEY-V C H VERLAG GMBH, POSTFACH 101161, 69451 WEINHEIM, GERMANY
Keywords:	Synthetic methods; Nitrogen heterocycles; Regioselectivity; Rearrangement; Difunctionalization
Department/Centre:	Division of Chemical Sciences > Organic Chemistry
Date Deposited:	30 Jun 2016 05:12
Last Modified:	30 Jun 2016 05:12
URI:	http://eprints.iisc.ac.in/id/eprint/54098

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