Unprecedented access to functionalized pyrrolo[2,1-a]isoquinolines from the domino reaction of isoquinolinium ylides and electrophilic benzannulated heterocycles
Author:
Affiliation:
1. Chemical Sciences and Technology Division
2. CSIR-National Institute for Interdisciplinary Science and Technology (CSIR-NIIST)
3. Thiruvananthapuram 695019
4. India
5. Academy of Scientific and Innovative Research (AcSIR)
Abstract
The reaction between electrophilic benzannulated heterocycles and isoquinolinium methylides results in a domino dipolar cycloaddition-ring opening transformation, generating functionalized pyrrolo[2,1-a]isoquinolines and S–S-bridged bis-pyrrolo[2,1-a]isoquinolines.
Funder
Council of Scientific and Industrial Research
University Grants Commission
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2021/OB/D1OB00005E
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5. Tandem Reactions of Electrophilic Indoles toward Indolizines and Their Subsequent Transformations through Pd(II)-Mediated C–H Functionalization to Access Polyring-Fused N-Heterocycles;ACS Omega;2024-03-30
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