Substituent effect on regioselectivity in the di-pi-methane rearrangement: synthesis of disubstituted benzobarrelene derivatives and their photochemistry


Unaldi N., Balci M.

TETRAHEDRON LETTERS, vol.42, no.47, pp.8365-8367, 2001 (Journal Indexed in SCI) identifier identifier

  • Publication Type: Article / Article
  • Volume: 42 Issue: 47
  • Publication Date: 2001
  • Doi Number: 10.1016/s0040-4039(01)01770-1
  • Title of Journal : TETRAHEDRON LETTERS
  • Page Numbers: pp.8365-8367

Abstract

2,3- and 2,5-Dicyanobenzobarrelenes 5 and 6 have been synthesized and subjected to triplet-sensitized photoisomerization. 2,3-Dicyanobenzobarrelene 5 gave two di-pi -methane rearrangement products 7 and 8 and a [2 pi +2 pi] -cycloaddition product 9. However, 2,5-dicyanobenzobarrelene 6 formed a single di-Tc-methane product 13. The formation of these products is discussed in terms of the radical stabilizing effect of the substituents and the destabilizing effect on the formation of the cyclopropane ring, (C) 2001 Elsevier Science Ltd. All rights reserved.