Issue 8, 2021

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

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.

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

Supplementary files

Article information

Article type
Paper
Submitted
02 Jan 2021
Accepted
25 Jan 2021
First published
25 Jan 2021

Org. Biomol. Chem., 2021,19, 1807-1817

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

S. A. Babu, R. A. R., N. P. R., V. K. Omanakuttan, R. P., S. Varughese and J. John, Org. Biomol. Chem., 2021, 19, 1807 DOI: 10.1039/D1OB00005E

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