Total synthesis of (±)-Vertine with Z-selective RCM as a key step

Chausset-Boissarie, Laetitia; Arvai, Roman; Cumming, Graham R.; Besnard, Céline; Kundig, Ernst Peter

doi:10.1039/c0cc01885f

Scientific article

English

Total synthesis of (±)-Vertine with Z-selective RCM as a key step

ContributorsChausset-Boissarie, Laetitia; Arvai, Roman; Cumming, Graham R.; Besnard, Céline; Kundig, Ernst Peter

Published inChemical communications, vol. 46, no. 34, p. 6264-6266

Publication date2010

Abstract

A concise total synthesis of the strained pentacyclic alkaloid (±)-Vertine has been achieved in eleven steps with the key steps being pelletierine condensation, Suzuki–Miyaura coupling, and ring-closing metathesis.

Affiliation entities

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

Citation (ISO format)

CHAUSSET-BOISSARIE, Laetitia et al. Total synthesis of (±)-Vertine with Z-selective RCM as a key step. In: Chemical communications, 2010, vol. 46, n° 34, p. 6264–6266. doi: 10.1039/c0cc01885f

Article (Published version)

Identifiers

PID : unige:11663
DOI : 10.1039/c0cc01885f

Additional URL for this publicationhttp://xlink.rsc.org/?DOI=c0cc01885f

Journal ISSN1359-7345

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Total synthesis of (±)-Vertine with Z-selective RCM as a key step

A concise total synthesis of the strained pentacyclic alkaloid (±)-Vertine has been achieved in eleven steps with the key steps being pelletierine condensation, Suzuki–Miyaura coupling, and ring-closing metathesis.

Technical informations