UV-laser photochemistry: Retro-cleavage in the benzophenone-sensitized photolysis of Δ3-1,3,4-oxadiazolines into diazoalkanes

DOI: 10.1016/S0040-4039(00)94648-3

Source and publish data:

Tetrahedron Letters p. 863 - 866 (1990)

Update date:2022-08-04

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Authors:

Adam, Waldemar

Finzel, Ralf

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Article abstract of DOI:10.1016/S0040-4039(00)94648-3

Triplet-sensitized photolysis of 2-methoxy-2,5,5-trimethyl-Δ³-1,3,4-oxadiazoline (1a) led to the retro-cleavage products diazoalkane 2a and the ester 3a, for which the triplet diazenyl diradical 6a is postulated as precursor.

Full text of DOI:10.1016/S0040-4039(00)94648-3

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