The ring-closing olefin metathesis (RCM) of 2,2¢-divinylbiphenyls, using a second-generation RCM ruthenium-based catalyst, leads to differently substituted phenanthrenes in quantitative yield under very mild reaction conditions, independent of both nature and position of the groups present on the biphenyl moiety.

Ring-Closing Olefin Metathesis of 2,2'-Divinylbiphenyls: A Novel and General Approach to Phenanthrenes

Fabbri D
2004

Abstract

The ring-closing olefin metathesis (RCM) of 2,2¢-divinylbiphenyls, using a second-generation RCM ruthenium-based catalyst, leads to differently substituted phenanthrenes in quantitative yield under very mild reaction conditions, independent of both nature and position of the groups present on the biphenyl moiety.
2004
Istituto di Chimica Biomolecolare - ICB - Sede Pozzuoli
ORGANIC-SYNTHESIS
DERIVATIVES
CATALYSTS
PHOTOCYCLIZATION
ALDEHYDES
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/164952
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