Homocoupling of alkyl-, alkenyl-, and arylboronic acids

J. R. Falck, Suchismita Mohapatra, Muralidhar Bondlela, Sylesh K. Venkataraman

Research output: Contribution to journalArticle

51 Citations (Scopus)

Abstract

Alkyl-, alkenyl-, and arylboronic acids undergo Ag2O/CrCl2 mediated homocoupling in moderate to good yields under mild conditions. The general utility of this methodology is illustrated by an intramolecular annulation between sp and sp3 centers.

Original languageEnglish (US)
Pages (from-to)8149-8151
Number of pages3
JournalTetrahedron Letters
Volume43
Issue number45
DOIs
StatePublished - Nov 4 2002

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Acids

Keywords

  • Annulation
  • Boron
  • Chromium
  • Coupling reactions
  • Dimerisation

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Homocoupling of alkyl-, alkenyl-, and arylboronic acids. / Falck, J. R.; Mohapatra, Suchismita; Bondlela, Muralidhar; Venkataraman, Sylesh K.

In: Tetrahedron Letters, Vol. 43, No. 45, 04.11.2002, p. 8149-8151.

Research output: Contribution to journalArticle

Falck, JR, Mohapatra, S, Bondlela, M & Venkataraman, SK 2002, 'Homocoupling of alkyl-, alkenyl-, and arylboronic acids', Tetrahedron Letters, vol. 43, no. 45, pp. 8149-8151. https://doi.org/10.1016/S0040-4039(02)01897-X
Falck, J. R. ; Mohapatra, Suchismita ; Bondlela, Muralidhar ; Venkataraman, Sylesh K. / Homocoupling of alkyl-, alkenyl-, and arylboronic acids. In: Tetrahedron Letters. 2002 ; Vol. 43, No. 45. pp. 8149-8151.
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