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

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