Photochemical Rearrangement of 8- methyl Spiro [2.5] oct-7-en-4-one to 4-methyl Spiro [2.5] oct-4-en-6-one

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Abstract:

Irradiation of &methyl spiro [2.5] oct-7-en-4-one through its singlet excited state resulted in the formation of 4-methyl spirO [2.5] oct-4-en -6-one. We have used the cyclopropyl moiety in the molecule as a probe to study the operating mechanism in the photochemistry of ?, ?-unsaturated compounds. The results showed that this photoisomerization probably occurs through a concerted process.

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irradiation of &methyl; spiro [2.5] oct-7-en-4-one through its singlet excited state resulted in the formation of 4-methyl spiro [2.5] oct-4-en -6-one. we have used the cyclopropyl moiety in the molecule as a probe to study the operating mechanism in the photochemistry of ?, ?-unsaturated compounds. the results showed that this photoisomerization probably occurs through a concerted process.

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Journal title

volume 1  issue 1

pages  -

publication date 1989-12-01

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