摘要
The photoinduced intramolecular meta-cycloaddition of bichromophores 1a-1d gave diastereoselectively two types of adducts 2a-2d and 3a-3d respectively. The observed stereochemistry of cycloaddition is rationalized in terms of hydrogen bond effect induced by the 4hydroxy group in the 5-phenylpent-1-ene skeleton.
The photoinduced intramolecular meta-cycloaddition of bichromophores 1a-1d gave diastereoselectively two types of adducts 2a-2d and 3a-3d respectively. The observed stereochemistry of cycloaddition is rationalized in terms of hydrogen bond effect induced by the 4hydroxy group in the 5-phenylpent-1-ene skeleton.