Synthetic Advances in the C–H Activation of Rigid Scaffold Molecules

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DC Field	Value	Language
dc.contributor.author	Grover, Nitika	-
dc.date.accessioned	2024-08-10T04:07:06Z	-
dc.date.available	2024-08-10T04:07:06Z	-
dc.date.issued	2020	-
dc.identifier.uri	https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0040-1707884	-
dc.identifier.uri	http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/15183	-
dc.description.abstract	The remarkable structural and electronic properties of rigid non-conjugated hydrocarbons afford attractive opportunities to design molecular building blocks for both medicinal and material applications. The bridgehead positions provide the possibility to append diverse functional groups at specific angles and in specific orientations. The current review summarizes the synthetic development in CH functionalization of three rigid scaffolds namely: (a) cubane, (b) bicyclo[1.1.1]pentane (BCP), (c) adamantane.	en_US
dc.language.iso	en	en_US
dc.publisher	Thieme	en_US
dc.subject	Chemistry	en_US
dc.subject	Cubane	en_US
dc.subject	Bicyclo[1.1.1]pentane	en_US
dc.subject	Adamantane	en_US
dc.subject	Rigid scaffolds	en_US
dc.subject	CH-functionalization	en_US
dc.title	Synthetic Advances in the C–H Activation of Rigid Scaffold Molecules	en_US
dc.type	Article	en_US
Appears in Collections:	Department of Chemistry

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