Synthesis of tetrahydrofurocarbozolones via intramolecular Diels-Alder reactions

DOI: 10.1016/S0040-4039(00)73719-1

Source and publish data:

Tetrahedron Letters p. 6237 - 6240 (1993)

Update date:2022-08-03

Topics: Synthesis Intramolecular Diels-Alder Reactions

Authors:

Madalengoitia

Macdonald

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Article abstract of DOI:10.1016/S0040-4039(00)73719-1

10-Aryl-3a,4,10,10a-tetrahydrofuro[3,4-b]carbazol-1-ones were synthesized by an intramolecular Diels-Alder reaction. Exo/endo product ratios were found to be sensitive to both solvent and temperature. The synthesis of isoelliptitoxin 2, a hybrid molecule

Full text of DOI:10.1016/S0040-4039(00)73719-1

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