902463-86-9Relevant academic research and scientific papers
Radical-induced cyclopentannulation of Henry (nitroaldol)-derived intermediates
Luzzio, Frederick A.,Ott, Joel P.,Duveau, Damien Y.
, p. 5027 - 5030 (2007/10/03)
Tributyltin hydride-mediated cyclizations of 1-nitro-2-acetoxy-5-hexenes 7a-g having multiple substitutions on carbons 1 and 6 result in 2,3-substituted-1-acetoxycyclopentanes 1a-g. The substrates were prepared by nitroaldol reactions of silyloxyaldehydes
