Base-Mediated One-pot Synthesis of Oxygen-Based Heterocycles from 2-Hydroxyphenyl-Substituted para-Quinone Methides

Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2341

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DC Field	Value	Language
dc.contributor.author	Singh, Gurpreet	-
dc.contributor.author	Kumar, Suresh	-
dc.contributor.author	Chowdhury, Arjun	-
dc.contributor.author	Anand, R.V.	-
dc.date.accessioned	2020-11-27T09:42:16Z	-
dc.date.available	2020-11-27T09:42:16Z	-
dc.date.issued	2019	-
dc.identifier.citation	Journal of Organic Chemistry, 84(24),pp. 15978–15989.	en_US
dc.identifier.other	https://doi.org/10.1021/acs.joc.9b02455	-
dc.identifier.uri	https://pubs.acs.org/doi/abs/10.1021/acs.joc.9b02455	-
dc.identifier.uri	http://hdl.handle.net/123456789/2341	-
dc.description.abstract	One-pot synthesis of oxygen-containing heterocycles has been achieved through alkylation/acylation of 2-hydroxyphenyl-substituted para-quinone methides followed by an intramolecular 1,6-conjugate addition/cyclization and oxidation sequence. This protocol provides access to a wide range of oxygen-based heterocycles, such as 2,3-disubstituted benzo[b]furans, 2,3-dihydrobenzofurans and diaryl-substituted coumarin derivatives in moderate to good yields.	en_US
dc.language.iso	en	en_US
dc.publisher	American Chemical Society	en_US
dc.subject	Oxygen	en_US
dc.subject	Heterocycles	en_US
dc.subject	Synthesis	en_US
dc.title	Base-Mediated One-pot Synthesis of Oxygen-Based Heterocycles from 2-Hydroxyphenyl-Substituted para-Quinone Methides	en_US
dc.type	Article	en_US
Appears in Collections:	Research Articles

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