Substrate controlled, regioselective carbopalladation for the one-pot synthesis of C4-substituted tetrahydroisoquinoline analogues

Author:

Krishna Reddy Singarajanahalli Mundarinti12345,Suresh Pavithira12345,Thamotharan Subbiah67238ORCID,Nanubolu Jagadeesh Babu910115,Suresh Surisetti1210115ORCID,Selva Ganesan Subramaniapillai12345ORCID

Affiliation:

1. Department of Chemistry

2. School of Chemical and Biotechnology

3. SASTRA Deemed University

4. Thanjavur-613401

5. India

6. Biomolecular Crystallography Laboratory

7. Department of Bioinformatics

8. Thanjavur 613401

9. Centre for X-ray Crystallography

10. CSIR-Indian Institute of Chemical Technology

11. Hyderabad-500007

12. Organic Synthesis & Process Chemistry

Abstract

6-Exo-trig cyclization reaction through regioselective carbopalladation was demonstrated with N-(2-halobenzyl)-N-allylamines to furnish the corresponding C4-substituted tetrahydroisoquinoline derivatives.

Funder

Council of Scientific and Industrial Research, India

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

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