Tandem ring expansion/aldol cyclization of bicyclo[5.4.01, 7]undecanediones Academic Article uri icon

Overview

MeSH Major

  • Magnetic Resonance Imaging
  • Muscle, Skeletal
  • Muscular Diseases
  • Oxygen

abstract

  • Diazomethane ring expansion of 3 followed by deketalization, led to the formation of bicyclodione intermediates 6 and 8. These intermediates underwent internal aldol cyclization to give the tricyclic adducts 7 and 9 in a 1:1 ratio, respectively. © 2001 Elsevier Science Ltd. All rights reserved.

publication date

  • January 2002

Research

keywords

  • Academic Article

Identity

Digital Object Identifier (DOI)

  • 10.1016/S0040-4039(01)02072-X

Additional Document Info

start page

  • 33

end page

  • 35

volume

  • 43

number

  • 1