Annulative Morita–Baylis–Hillman reaction to synthesise chiral dibenzocycloheptanes

Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/4836

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DC Field	Value	Language
dc.contributor.author	Mondal, Atanu	-
dc.contributor.author	Shivangi	-
dc.contributor.author	Tung, Pinku	-
dc.contributor.author	Waguldea, Siddhant V.	-
dc.contributor.author	Ramasastry, S. S. V.	-
dc.date.accessioned	2023-08-18T10:58:12Z	-
dc.date.available	2023-08-18T10:58:12Z	-
dc.date.issued	2021	-
dc.identifier.citation	Chemical Communications, 57(73), 9260–9263.	en_US
dc.identifier.uri	https://pubs.rsc.org/en/content/articlelanding/2021/CC/D1CC02765D	-
dc.identifier.uri	http://hdl.handle.net/123456789/4836	-
dc.description	Only IISER Mohali authors are available in the record	en_US
dc.description.abstract	We describe the first metal-free and organocatalytic strategy to access highly functionalised dibenzocycloheptanes via a phosphine-promoted annulative Morita–Baylis–Hillman (MBH) reaction. The method is manipulated to access to chiral dibenzocycloheptanes as well. This work represents a rare entry for the construction of seven-membered carbocycles via the MBH route. The realisation of several bioactive molecules possessing the dibenzocycloheptane core makes this an attractive strategy.	en_US
dc.language.iso	en_US	en_US
dc.publisher	Publishing	en_US
dc.subject	Morita–Baylis–Hillman	en_US
dc.subject	dibenzocycloheptanes	en_US
dc.title	Annulative Morita–Baylis–Hillman reaction to synthesise chiral dibenzocycloheptanes	en_US
dc.type	Article	en_US
Appears in Collections:	Research Articles

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