Synthesis of α-onoceradiene-like terpene dimers by intermolecular metathesis processes

María C. De La Torre; Antonio M. Deometrio; Elsa Álvaro; Isabel García; Miguel A. Sierra

doi:10.1021/ol052680m

Synthesis of α-onoceradiene-like terpene dimers by intermolecular metathesis processes

María C. De La Torre^*, Antonio M. Deometrio, Elsa Álvaro, Isabel García, Miguel A. Sierra

^*Corresponding author for this work

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Abstract

New α-onoceradiene analogues having a terpene homodimer skeleton are accessible from Weinreb's amide 2 derived from commercial (R)-(+)-sclareolide using an intermolecular metathesis reaction as the key step to build the linker joining both terpene moieties.

Original language	English (US)
Pages (from-to)	593-596
Number of pages	4
Journal	Organic Letters
Volume	8
Issue number	4
DOIs	https://doi.org/10.1021/ol052680m
State	Published - Feb 16 2006

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/ol052680m

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title = "Synthesis of α-onoceradiene-like terpene dimers by intermolecular metathesis processes",

abstract = "New α-onoceradiene analogues having a terpene homodimer skeleton are accessible from Weinreb's amide 2 derived from commercial (R)-(+)-sclareolide using an intermolecular metathesis reaction as the key step to build the linker joining both terpene moieties.",

author = "{De La Torre}, {Mar{\'i}a C.} and Deometrio, {Antonio M.} and Elsa {\'A}lvaro and Isabel Garc{\'i}a and Sierra, {Miguel A.}",

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T1 - Synthesis of α-onoceradiene-like terpene dimers by intermolecular metathesis processes

AU - De La Torre, María C.

AU - Deometrio, Antonio M.

AU - Álvaro, Elsa

AU - García, Isabel

AU - Sierra, Miguel A.

PY - 2006/2/16

Y1 - 2006/2/16

N2 - New α-onoceradiene analogues having a terpene homodimer skeleton are accessible from Weinreb's amide 2 derived from commercial (R)-(+)-sclareolide using an intermolecular metathesis reaction as the key step to build the linker joining both terpene moieties.

AB - New α-onoceradiene analogues having a terpene homodimer skeleton are accessible from Weinreb's amide 2 derived from commercial (R)-(+)-sclareolide using an intermolecular metathesis reaction as the key step to build the linker joining both terpene moieties.

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Synthesis of α-onoceradiene-like terpene dimers by intermolecular metathesis processes

Abstract

ASJC Scopus subject areas

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