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

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