“…This is observed in the reversible ring opening and ring closing of the dissymmetric cage compounds (Scheme 13) formed from substituted cyclopentadienones 318 . The synthesis of cage compounds related to this and others has been reviewed 319 . Irradiation of adducts 490 and 491 at 260 nm, where the benzenoid moiety absorbs, results in efficient (φ can be as high as 0.5) conversion to the corresponding naphthalene derivatives 320 .…”
Section: Cyclobutane Ring Opening Reactionsmentioning
Introduction
Cycloaddition Reactions Involving Alkenes
Cycloaddition Reactions Involving Dienes and Trienes
Cycloadditions of Enones and Related Compounds
Photochemistry of Ketones
Cage Compounds
Cyclobutane Ring Opening Reactions
“…This is observed in the reversible ring opening and ring closing of the dissymmetric cage compounds (Scheme 13) formed from substituted cyclopentadienones 318 . The synthesis of cage compounds related to this and others has been reviewed 319 . Irradiation of adducts 490 and 491 at 260 nm, where the benzenoid moiety absorbs, results in efficient (φ can be as high as 0.5) conversion to the corresponding naphthalene derivatives 320 .…”
Section: Cyclobutane Ring Opening Reactionsmentioning
Introduction
Cycloaddition Reactions Involving Alkenes
Cycloaddition Reactions Involving Dienes and Trienes
Cycloadditions of Enones and Related Compounds
Photochemistry of Ketones
Cage Compounds
Cyclobutane Ring Opening Reactions
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