A recyclable fluorous organocatalyst for Diels-Alder reactions

Qianli Chu; Wei Zhang; Dennis P. Curran

doi:10.1016/j.tetlet.2006.10.101

A recyclable fluorous organocatalyst for Diels-Alder reactions

Qianli Chu
, Wei Zhang
, Dennis P. Curran

Chemistry

University of Pittsburgh

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

Abstract

Chiral fluorous imidazolidinone catalyst 2 provides consistently high enantioselectivities in Diels-Alder reactions of dienes and α,β-unsaturated aldehydes. The catalyst can be readily separated from the reaction products by fluorous solid-phase extraction, and recovered in excellent purity for direct reuse.

Original language	English
Pages (from-to)	9287-9290
Number of pages	4
Journal	Tetrahedron Letters
Volume	47
Issue number	52
DOIs	https://doi.org/10.1016/j.tetlet.2006.10.101
State	Published - Dec 25 2006

ASJC Scopus Subject Areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/j.tetlet.2006.10.101

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title = "A recyclable fluorous organocatalyst for Diels-Alder reactions",

abstract = "Chiral fluorous imidazolidinone catalyst 2 provides consistently high enantioselectivities in Diels-Alder reactions of dienes and α,β-unsaturated aldehydes. The catalyst can be readily separated from the reaction products by fluorous solid-phase extraction, and recovered in excellent purity for direct reuse.",

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AB - Chiral fluorous imidazolidinone catalyst 2 provides consistently high enantioselectivities in Diels-Alder reactions of dienes and α,β-unsaturated aldehydes. The catalyst can be readily separated from the reaction products by fluorous solid-phase extraction, and recovered in excellent purity for direct reuse.

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UR - https://www.scopus.com/pages/publications/33751194087#tab=citedBy

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M3 - Article

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EP - 9290

JO - Tetrahedron Letters

JF - Tetrahedron Letters

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A recyclable fluorous organocatalyst for Diels-Alder reactions

Abstract

ASJC Scopus Subject Areas

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