Stereoselective synthesis of configurationally stable functionalized ethano-bridged Tröger bases

Michon, Christophe; Sharma, Ankit; Bernardinelli, Gérald Hugues; Francotte, Eric; Lacour, Jérôme

doi:10.1039/b925065d

Scientific article

English

Stereoselective synthesis of configurationally stable functionalized ethano-bridged Tröger bases

ContributorsMichon, Christophe; Sharma, Ankit; Bernardinelli, Gérald Hugues; Francotte, Eric; Lacour, Jérôme

Published inChemical communications, vol. 46, no. 13, p. 2206-2208

Publication date2010

Abstract

New functionalized ethano-bridged Tröger bases are readily prepared using a simple alkylation/rearrangement sequence which affords configurationally stable derivatives as single stereoisomers (de > 96%).

Affiliation

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

Citation (ISO format)

MICHON, Christophe et al. Stereoselective synthesis of configurationally stable functionalized ethano-bridged Tröger bases. In: Chemical communications, 2010, vol. 46, n° 13, p. 2206–2208. doi: 10.1039/b925065d

Article (Published version)

Identifiers

PID : unige:5474
DOI : 10.1039/b925065d

ISSN of the journal1359-7345

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Stereoselective synthesis of configurationally stable functionalized ethano-bridged Tröger bases

New functionalized ethano-bridged Tröger bases are readily prepared using a simple alkylation/rearrangement sequence which affords configurationally stable derivatives as single stereoisomers (de > 96%).

Technical informations