Intramolecular meta photocycloaddition of conformationally restrained 5-phenylpent-1-enes. Part II: Steric and electronic effects caused by 4-mono- and 4-disubstitution

Author:

Barentsen Helma M.,Sieval Alex B.,Cornelisse Jan

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference41 articles.

1. Barentsen, H.M.; Talman, E.G.; Piet, D.P. and Cornelisse, J., Tetrahedron, in press.

2. Substituent effects on the intramolecular photochemical reactions of phenyl–ethenyl non-conjugated bichromophoric systems

3. The second letter, x or y, denotes the stereochemistry of the substituted carbon: x when the substituent on the β-carbon atoms is endo, y when it is exo. When two substituents are present on the β-carbon atom, the structure is indicated with x if the oxygen-containing substituent is endo.

4. The meta photocycloaddition of arenes to alkenes

5. Factors affecting ease of ring formation. The effect of anchoring substitution on the rate of an intramolecular diels-alder reaction with furan-diene

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