Diels - Alder reactions of epoxybutene derivatives and subsequent synthetic manipulations of the cycloadducts

Marion A Franks; John A. Hyatt; Mark E. Welker

doi:10.1021/op010219d

Diels - Alder reactions of epoxybutene derivatives and subsequent synthetic manipulations of the cycloadducts

Marion A Franks
, John A. Hyatt
, Mark E. Welker

Chemistry

Wake Forest University
Eastman Chemical Company

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

4 Scopus citations

Abstract

Diels - Alder reactions between cyclopentadiene, cyclohexadiene, and a number of epoxybutene derivatives are reported. The endo diastereomer from the Diels - Alder reaction of cyclopentadiene with 2,5-dihydrofuran was functionalized by additional oxidative transformations.

Original language	English
Pages (from-to)	514-518
Number of pages	5
Journal	Organic Process Research and Development
Volume	5
Issue number	5
DOIs	https://doi.org/10.1021/op010219d
State	Published - Sep 1 2001

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10.1021/op010219d

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title = "Diels - Alder reactions of epoxybutene derivatives and subsequent synthetic manipulations of the cycloadducts",

abstract = "Diels - Alder reactions between cyclopentadiene, cyclohexadiene, and a number of epoxybutene derivatives are reported. The endo diastereomer from the Diels - Alder reaction of cyclopentadiene with 2,5-dihydrofuran was functionalized by additional oxidative transformations.",

author = "Franks, \{Marion A\} and Hyatt, \{John A.\} and Welker, \{Mark E.\}",

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AU - Franks, Marion A

AU - Hyatt, John A.

AU - Welker, Mark E.

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N2 - Diels - Alder reactions between cyclopentadiene, cyclohexadiene, and a number of epoxybutene derivatives are reported. The endo diastereomer from the Diels - Alder reaction of cyclopentadiene with 2,5-dihydrofuran was functionalized by additional oxidative transformations.

AB - Diels - Alder reactions between cyclopentadiene, cyclohexadiene, and a number of epoxybutene derivatives are reported. The endo diastereomer from the Diels - Alder reaction of cyclopentadiene with 2,5-dihydrofuran was functionalized by additional oxidative transformations.

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Diels - Alder reactions of epoxybutene derivatives and subsequent synthetic manipulations of the cycloadducts

Abstract

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