First Synthesis of 2-Vinylindole and its Diels-Alder Reactions with CC-Dienophiles

DOI: 10.1002/hlca.19880710517

Source and publish data:

Helvetica Chimica Acta p. 1060 - 1064 (1988)

Update date:2022-08-11

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Authors:

Pindur, Ulf

Eitel, Manfred

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Article abstract of DOI:10.1002/hlca.19880710517

By means of an intramolecular Wittig process, 2-vinylindole (2) was prepared.The indole 2 functions as a heterocyclic, donor-activated 1,3-diene and undergoes <4+2> cycloaddition reactions with dimethyl acetylenedicarboxylate, N-phenylmaleimide, and p-ben

Full text of DOI:10.1002/hlca.19880710517

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