Issue 14, 1974

Quenching of the excited singlet penta-1,3-dienes by Me3SnH: evidence against the allylmethylene configuration of the relaxed S1 state

Abstract

The 1,4 concerted addition of Me3SnH to the singlet excited penta-1,3-dienes yields cis- and trans- adducts according to a stereochemistry which is incompatible with an allylmethylene relaxed configuration and suggests a doubly state.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1974, 529-530

Quenching of the excited singlet penta-1,3-dienes by Me3SnH: evidence against the allylmethylene configuration of the relaxed S1 state

M. Bigwood and S. Boué, J. Chem. Soc., Chem. Commun., 1974, 529 DOI: 10.1039/C39740000529

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