REACTIVITY OF PHENYL(TOLYLSULFONYL)ACETYLENE TOWARDS DIENES AND HOMO-DIENES: CYCLOADDITIONS VERSUS FRAGMENTATION-ADDITION REACTIONS

DOI: 10.1016/S0040-4039(00)80222-1

Source and publish data:

Tetrahedron Letters p. 831 - 834 (1988)

Update date:2022-07-30

Topics:

Authors:

Lucchi, Ottorino De

Licini, Guilia

Pasquato, Lucia

Senta, Marina

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Article abstract of DOI:10.1016/S0040-4039(00)80222-1

Depending upon the diene, phenyl(tolylsulfonyl)acetylene (1a) affords the (4+2), the (2+2)-cycloadducts or products derived by 1,4-addition of the two fragments formed from homolytic cleavage of the carbon-sulfur bond.

Full text of DOI:10.1016/S0040-4039(00)80222-1

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