PHOTOCYCLOADDITION OF N-METHYLTHIOPHTHALIMIDE WITH ALKYNES

DOI: 10.1016/S0040-4039(00)98974-3

Source and publish data:

Tetrahedron Letters p. 2249 - 2252 (1985)

Update date:2022-08-11

Topics:

Authors:

Coyle, J. D.

Rapley, P. A.

Kamphuis, J.

Bos, H. J. T.

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Article abstract of DOI:10.1016/S0040-4039(00)98974-3

N-Methylthiophthalimide undergoes photochemical cycloaddition reactions with diphenylacetylene, hex-3-yne and bis(methylthio)acetylene to form spiro-thietes; in solution the spiro-thiete from the bis(methylthio)alkyne is in equilibrium with its ring-opened isomer.

Full text of DOI:10.1016/S0040-4039(00)98974-3

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Product name:Spiro[1H-isoindole-1,2'-[2H]thiet]-3(2H)-one, 2-methyl-3',4'-diphenyl-

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