Ring expansion of an antiaromatic beryllole: synthesis of novel five-, seven- and nine-membered beryllacycles

Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/18016

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DC Field	Value	Language
dc.contributor.author	Roy, Dipak Kumar	en_US
dc.date.accessioned	2026-03-12T10:55:39Z	-
dc.date.available	2026-03-12T10:55:39Z	-
dc.date.issued	2026	-
dc.identifier.citation	Tröster, T., Saha, K., Roy, D. K., Dewhurst, R. D., & Braunschweig, H. (2026). Ring expansion of an antiaromatic beryllole: synthesis of novel five-, seven- and nine-membered beryllacycles. Chemical Communications. https://doi.org/10.1039/d5cc05783c	en_US
dc.identifier.issn	1359-7345	-
dc.identifier.other	EID(2-s2.0-105030491573)	-
dc.identifier.uri	https://dx.doi.org/10.1039/d5cc05783c	-
dc.identifier.uri	https://dspace.iiti.ac.in:8080/jspui/handle/123456789/18016	-
dc.description.abstract	This study investigates the reactivity of a beryllole and presents the first comparison between this antiaromatic species and its boron analogue, borole. The reaction of a beryllole with small molecules and unsaturated substrates led to ring expansion reactions or the insertion of atoms into the beryllole ring and the formation of five-, seven- or nine-membered beryllium-containing heterocyclic rings. This journal is © The Royal Society of Chemistry, 2026	en_US
dc.language.iso	en	en_US
dc.publisher	Royal Society of Chemistry	en_US
dc.source	Chemical Communications	en_US
dc.title	Ring expansion of an antiaromatic beryllole: synthesis of novel five-, seven- and nine-membered beryllacycles	en_US
dc.type	Journal Article	en_US
Appears in Collections:	Department of Chemistry

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