The synthesis of (±)-cavernosine

Jefford, Charles; Jaggi, Danielle; Bernardinelli, Gérald Hugues; Boukouvalas, John

doi:10.1016/S0040-4039(01)83856-9

Scientific article

English

The synthesis of (±)-cavernosine

ContributorsJefford, Charles; Jaggi, Danielle; Bernardinelli, Gérald Hugues; Boukouvalas, John

Published inTetrahedron letters, vol. 28, no. 35, p. 4041-4044

Publication date1987

Abstract

The title compound and its epimer were synthesized in three and two steps from dihydro-β-ionone and 2-trimethylsiloxyfuran in 38 and 63% overall yields respectively. Their relative configurations were confirmed by X-ray of an intermediate.

Affiliation

Faculté des sciences / Section de chimie et biochimie / Département de chimie organique

Citation (ISO format)

JEFFORD, Charles et al. The synthesis of (±)-cavernosine. In: Tetrahedron letters, 1987, vol. 28, n° 35, p. 4041–4044. doi: 10.1016/S0040-4039(01)83856-9

Article (Published version)

Identifiers

PID : unige:166820
DOI : 10.1016/S0040-4039(01)83856-9

Commercial URLhttps://linkinghub.elsevier.com/retrieve/pii/S0040403901838569

ISSN of the journal0040-4039

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The synthesis of (±)-cavernosine

The title compound and its epimer were synthesized in three and two steps from dihydro-β-ionone and 2-trimethylsiloxyfuran in 38 and 63% overall yields respectively. Their relative configurations were confirmed by X-ray of an intermediate.

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