GENERATION AND CYCLOADDITIONS OF 2-(N-ACYLAMINO)-1-THIA-1,3-DIENES. PART II. RATIONALIZATION OF REACTIVITY USING AN FMO APPROACH.

DOI: 10.1016/S0040-4020(01)85801-4

Source and publish data:

Tetrahedron p. 7879 - 7898 (1989)

Update date:2022-09-26

Topics:

Authors:

Barnish, Ian T.

Fishwick, Colin W. G.

Hill, David R.

Szantay, Csaba

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Article abstract of DOI:10.1016/S0040-4020(01)85801-4

2-(N-Acylamino)-1-thia-1,3-dienes undergo regiospecific and stereoselective Diels-Alder cycloaddition to electron deficient, non-activated, and electron rich alkenes to give usefully functionalised dihydrothiopyrans in good yields.

Full text of DOI:10.1016/S0040-4020(01)85801-4

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