Accessing Highly Functionalized Cyclopentanoids: Via a Cascade Palladation Approach: Unprecedented Benzylic C-H Activation Towards Cyclopentenoindanes

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DC Field	Value	Language
dc.contributor.author	Santhini, P V	-
dc.contributor.author	Smrithy, A S	-
dc.contributor.author	Irfana Jesin, C P	-
dc.contributor.author	Sunil Varughese	-
dc.contributor.author	Jubi John	-
dc.contributor.author	Radhakrishnan, K V	-
dc.date.accessioned	2018-06-01T07:16:19Z	-
dc.date.available	2018-06-01T07:16:19Z	-
dc.date.issued	2018-02-23	-
dc.identifier.citation	Chemical Communications, 54(24):2982-2985	en_US
dc.identifier.uri	http://10.10.100.66:8080/xmlui/handle/123456789/3075	-
dc.description.abstract	A Pd-catalyzed synthesis of 3,4,5-trisubstituted cyclopentenes from diazabicyclic olefins and o-iodobenzoates has been developed. The hitherto unknown cascade process involves three stages: carbopalladation, oxypalladation and a Tsuji–Trost reaction. We have also developed a facile route involving a novel benzylic C–H activation towards cyclopentenoindane moieties.	en_US
dc.language.iso	en	en_US
dc.publisher	The Royal Society of Chemistry	en_US
dc.title	Accessing Highly Functionalized Cyclopentanoids: Via a Cascade Palladation Approach: Unprecedented Benzylic C-H Activation Towards Cyclopentenoindanes	en_US
dc.type	Article	en_US
Appears in Collections:	2018

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