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Synthesis 2003(14): 2115-2134
DOI: 10.1055/s-2003-42082
DOI: 10.1055/s-2003-42082
REVIEW
© Georg Thieme Verlag Stuttgart · New York
Cyclisations Involving Attack of Carbo- and Heteronucleophiles on Carbon-Carbon π-Bonds Activated by Organopalladium Complexes
Weitere Informationen
Received
10 February 2003
Publikationsdatum:
24. September 2003 (online)
Publikationsverlauf
Publikationsdatum:
24. September 2003 (online)
Abstract
In the late 1980’s, a new process based on an intramolecular palladium-mediated cyclisation coupled with a carbon-carbon bond forming reaction appeared in the literature. Since the first report, many novel ring systems have been synthesized using this methodology. The aim of this present review article is to summarise a number of synthetic applications of this new process developed over the last fifteen years.
1 Introduction
2 Carbocycles
2.1 Cyclisation Unactivated Olefins
2.2 Cyclisation of Unactivated Alkynes
3 Heterocycles
3.1 Oxygen Heterocycles
3.2 Nitrogen Heterocycles
4 Conclusion
Key words
catalysis - palladium - carbocycles - heterocycles - cyclisation
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References
A similar duality (Heck reaction versus cyclisation reaction) depending on the strengh of the nucleophile was also observed in a palladium mediated cyclisation of olefins (see Scheme [8] ).