A new etherification reaction in the η4-dienyl-tricarbonyliron series: Access to the 2,5-disubstituted-1,4-dioxane core

J. P. Lellouche; C. Quirosa-Guillou

doi:10.1080/00397919508012659

A new etherification reaction in the η⁴-dienyl-tricarbonyliron series: Access to the 2,5-disubstituted-1,4-dioxane core

J. P. Lellouche, C. Quirosa-Guillou

Serv. des Molecules Marquees

Research output: Contribution to journal › Article › peer-review

4 Scopus citations

Abstract

The η⁴-dienyl tricarbonyliron complex 8 has been used as a valuable building block en route to the 2,5-disubstituted-1,4-dioxane 4. Particularly noteful is the new regioselective etherification reaction of 8 with the suitably protected secondary glycerol 11 through the non-isolated organometallic cation 13.

Original language	English
Pages (from-to)	977-993
Number of pages	17
Journal	Synthetic Communications
Volume	25
Issue number	7
DOIs	https://doi.org/10.1080/00397919508012659
State	Published - 1 Apr 1995
Externally published	Yes

Bibliographical note

Funding Information:
this work and the Servier Research Institute (Suresnes) for its financial support.

Funding

this work and the Servier Research Institute (Suresnes) for its financial support.

Funders	Funder number
Servier Research Institute

Access to Document

10.1080/00397919508012659

Cite this

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abstract = "The η4-dienyl tricarbonyliron complex 8 has been used as a valuable building block en route to the 2,5-disubstituted-1,4-dioxane 4. Particularly noteful is the new regioselective etherification reaction of 8 with the suitably protected secondary glycerol 11 through the non-isolated organometallic cation 13.",

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