SYNTHESIS AND DIELS-ALDER REACTIONS OF 5,5-DICYANOCYCLOPENTADIENE: REGIOSELECTIVE SYNTHESIS OF 1,5-DISUBSTITUTED-1,3-CYCLOHEXADIENES

DOI: 10.1016/S0040-4039(00)98312-6

Source and publish data:

Tetrahedron Letters p. 1691 - 1694 (1985)

Update date:2022-08-05

Topics:

Authors:

Dmitrienko, Gary I.

Savard, Marc E.

Friesen, Richard W.

Thandi, Mibbo S.

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Article abstract of DOI:10.1016/S0040-4039(00)98312-6

5,5-Dicyanocyclopentadiene, readily prepared in three steps from commercially available cis-1,4-dichloro-2-butene, undergoes Diels-Alder reactions with a number of dienophiles to give 5-substituted 7,7-dicyanobicyclo<2.2.1>hept-2-enes with high endo-selec

Full text of DOI:10.1016/S0040-4039(00)98312-6

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