Unprecedented access to functionalized pyrrolo[2,1-a]isoquinolines from the domino reaction of isoquinolinium ylides and electrophilic benzannulated heterocycles

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DC Field	Value	Language
dc.contributor.author	Babu, S A	-
dc.contributor.author	Rajalekshmi, A R	-
dc.contributor.author	Nitha, P R	-
dc.contributor.author	Omanakuttan, V K	-
dc.contributor.author	Rahul, P	-
dc.contributor.author	Varughese, S	-
dc.contributor.author	John, J	-
dc.date.accessioned	2021-10-27T08:21:27Z	-
dc.date.available	2021-10-27T08:21:27Z	-
dc.date.issued	2021	-
dc.identifier.citation	Organic & Biomolecular Chemistry; 19(8):1807-1817	en_US
dc.identifier.uri	https://pubs.rsc.org/en/content/articlelanding/2021/ob/d1ob00005e#!divAbstract	-
dc.identifier.uri	http://hdl.handle.net/123456789/3843	-
dc.description.abstract	We have come across an unexpected reaction between electrophilic indoles and isoquinolinium methylides for accessing functionalized pyrrolo[2,1-a]isoquinolines. The reaction was found in general to yield the products in good yields. We also observed the formation of S–S-bridged bis-pyrrolo[2,1-a]isoquinolines from the reaction of 3-nitro benzothiophene and isoquinolinium methylides.	en_US
dc.language.iso	en	en_US
dc.publisher	Royal Society of Chemistry	en_US
dc.title	Unprecedented access to functionalized pyrrolo[2,1-a]isoquinolines from the domino reaction of isoquinolinium ylides and electrophilic benzannulated heterocycles	en_US
dc.type	Article	en_US
Appears in Collections:	2021

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