SYNTHESIS OF 3-ω-EPOXIDO FARNESYL INDOLES, INTERMEDIATES IN THE BIOGENESIS OF SESQUITERPENIC INDOLE ALKALOIDS

DOI: 10.1016/S0040-4039(00)98704-5

Source and publish data:

Tetrahedron Letters p. 3985 - 3988 (1985)

Update date:2022-08-03

Topics:

Authors:

Mirand, Catherine

Maindreville, Michele Doee de

Levy, Jean

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Article abstract of DOI:10.1016/S0040-4039(00)98704-5

Epoxides 1a,b, the probable bioprecursors of a serie of indoloterpene alkaloids, were synthesized from indole and farnesyl bromides through application of the Van Tamelen regiospecific epoxidation process to the derived N-acylindolines 14a,b.

Full text of DOI:10.1016/S0040-4039(00)98704-5

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