This review is a detailed account of authors' work in the field of biomimetic cyclization of geraniol-like dienes. The very high regio- and enantioselectivity achieved made these elegant reactions a viable tool for the synthesis of monocyclic building blocks used in the synthesis of valued terpenoids, like the precious aroma and perfume constituents' ionones and irones.

Biomimetic cyclization of geraniol derivatives, a useful tool in the total synthesis of bioactive monocyclic terpenoids

Luparia, Marco;Porta, Alessio
Conceptualization
;
Zanoni, Giuseppe
Conceptualization
;
Vidari, Giovanni
Conceptualization
2011

Abstract

This review is a detailed account of authors' work in the field of biomimetic cyclization of geraniol-like dienes. The very high regio- and enantioselectivity achieved made these elegant reactions a viable tool for the synthesis of monocyclic building blocks used in the synthesis of valued terpenoids, like the precious aroma and perfume constituents' ionones and irones.
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11571/1212656
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