Highly efficient Meinwald rearrangement reactions of epoxides catalyzed by copper tetrafluoroborate

Mathew W. C. Robinson; Kathryn S. Pillinger; Andrew E. Graham

doi:10.1016/j.tetlet.2006.06.055

Highly efficient Meinwald rearrangement reactions of epoxides catalyzed by copper tetrafluoroborate

Mathew W. C. Robinson, Kathryn S. Pillinger, Andrew E. Graham^*

^*Corresponding author for this work

Faculty of Computing, Engineering and Science

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

54 Citations (Scopus)

Abstract

Epoxides undergo a highly efficient and selective rearrangement in the presence of catalytic quantities of copper tetrafluoroborate to give carbonyl compounds in excellent yields. The low toxicity and ease of handling of this reagent make it an attractive alternative to the more corrosive Lewis acids frequently employed.

Original language	English
Pages (from-to)	5919-5921
Number of pages	3
Journal	Tetrahedron Letters
Volume	47
Issue number	33
DOIs	https://doi.org/10.1016/j.tetlet.2006.06.055
Publication status	Published - 14 Aug 2006

Keywords

Copper tetrafluoroborate
Lewis acid catalyst
Meinwald rearrangement

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10.1016/j.tetlet.2006.06.055Licence: CC BY-NC-ND

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title = "Highly efficient Meinwald rearrangement reactions of epoxides catalyzed by copper tetrafluoroborate",

abstract = "Epoxides undergo a highly efficient and selective rearrangement in the presence of catalytic quantities of copper tetrafluoroborate to give carbonyl compounds in excellent yields. The low toxicity and ease of handling of this reagent make it an attractive alternative to the more corrosive Lewis acids frequently employed. ",

keywords = "Copper tetrafluoroborate, Lewis acid catalyst, Meinwald rearrangement",

author = "Robinson, {Mathew W. C.} and Pillinger, {Kathryn S.} and Graham, {Andrew E.}",

year = "2006",

month = aug,

day = "14",

doi = "10.1016/j.tetlet.2006.06.055",

language = "English",

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journal = "Tetrahedron Letters",

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T1 - Highly efficient Meinwald rearrangement reactions of epoxides catalyzed by copper tetrafluoroborate

AU - Robinson, Mathew W. C.

AU - Pillinger, Kathryn S.

AU - Graham, Andrew E.

PY - 2006/8/14

Y1 - 2006/8/14

N2 - Epoxides undergo a highly efficient and selective rearrangement in the presence of catalytic quantities of copper tetrafluoroborate to give carbonyl compounds in excellent yields. The low toxicity and ease of handling of this reagent make it an attractive alternative to the more corrosive Lewis acids frequently employed.

AB - Epoxides undergo a highly efficient and selective rearrangement in the presence of catalytic quantities of copper tetrafluoroborate to give carbonyl compounds in excellent yields. The low toxicity and ease of handling of this reagent make it an attractive alternative to the more corrosive Lewis acids frequently employed.

KW - Copper tetrafluoroborate

KW - Lewis acid catalyst

KW - Meinwald rearrangement

U2 - 10.1016/j.tetlet.2006.06.055

DO - 10.1016/j.tetlet.2006.06.055

M3 - Article

AN - SCOPUS:33745698155

VL - 47

SP - 5919

EP - 5921

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 33

ER -

Highly efficient Meinwald rearrangement reactions of epoxides catalyzed by copper tetrafluoroborate

Abstract

Keywords

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