Synthesis 2014; 46(13): 1739-1750
DOI: 10.1055/s-0033-1341239
paper
© Georg Thieme Verlag Stuttgart · New York

Nucleophilic Addition of Lewis Acid Complexed α-Amino Carbanions to Arynes: Synthesis of 1-Aryl-N-methyl-1,2,3,4-tetrahydroisoquinolines

Authors

  • Kamal Nain Singh*

    Department of Chemistry and Centre of Advanced Studies in Chemistry, Panjab University, Chandigarh 160014, India   Fax: +91(172)2545074   Email: kns@pu.ac.in
  • Paramjit Singh

    Department of Chemistry and Centre of Advanced Studies in Chemistry, Panjab University, Chandigarh 160014, India   Fax: +91(172)2545074   Email: kns@pu.ac.in
  • Esha Sharma

    Department of Chemistry and Centre of Advanced Studies in Chemistry, Panjab University, Chandigarh 160014, India   Fax: +91(172)2545074   Email: kns@pu.ac.in
  • Yadwinder Singh Deol

    Department of Chemistry and Centre of Advanced Studies in Chemistry, Panjab University, Chandigarh 160014, India   Fax: +91(172)2545074   Email: kns@pu.ac.in
Further Information

Publication History

Received: 13 February 2014

Accepted after revision: 28 March 2014

Publication Date:
12 May 2014 (online)


Graphical Abstract

Abstract

The direct C-1 arylation of N-methyl-1,2,3,4-tetrahydroisoquinolines via coupling of α-amino carbanions derived from Lewis acid complexed tetrahydroisoquinolines and in situ generated arynes is described. This process provides an easy access to the title compounds and a new synthetic route to (±)-cryptostyline alkaloids.

Supporting Information