Access to Naphthalene Derivatives from 2-Alkeny1-pheny1- substituted para-quinone methodes

Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/1909

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DC Field	Value	Language
dc.contributor.author	Prasad, Divyanshu Baranwal Shambhu	-
dc.date.accessioned	2022-12-17T04:58:56Z	-
dc.date.available	2022-12-17T04:58:56Z	-
dc.date.issued	2022-04	-
dc.identifier.uri	http://hdl.handle.net/123456789/1909	-
dc.description.abstract	A base-mediated and Lewis acid catalyzed one-pot reaction between 2-alkenylphenyl- substituted p-quinone methides and bromo-malonates has been developed to access a wide range of naphthalene derivatives. Basically, this transformation involves two different steps, i.e., (i) base-mediated cyclopropanation of 2-alkenylphenyl-substituted p-quinone methides with bromo-malonates (ii) Lewis acid catalyzed intramolecular annulation of cyclopropenyl- alkenes to form the naphthalene derivatives.	en_US
dc.language.iso	en_US	en_US
dc.publisher	IISER Mohali	en_US
dc.subject	substituted para-quinone	en_US
dc.subject	Naphthalene Derivatives	en_US
dc.subject	2-Alkeny1-pheny1	en_US
dc.title	Access to Naphthalene Derivatives from 2-Alkeny1-pheny1- substituted para-quinone methodes	en_US
dc.type	Thesis	en_US
Appears in Collections:	MS-17

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