A facile tetrahydrothiophene-catalyzed ylide route to vinyloxiranes

Kai Li; Xian Ming Deng; Yong Tang

doi:10.1039/b304443b

A facile tetrahydrothiophene-catalyzed ylide route to vinyloxiranes

Kai Li, Xian Ming Deng, Yong Tang

Multifunctional Equipment Integration

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28 Scopus citations

Abstract

Access to vinyloxiranes using aldehydes and allylic bromides in the presence of 1-5 mol% tetrahydrothiophene is reported. Both aliphatic and aromatic aldehydes work well in this reaction and the catalyst loading could be reduced as low as 0.5 mol%.

Original language	English
Pages (from-to)	2074-2075
Number of pages	2
Journal	Chemical Communications
Volume	3
Issue number	16
DOIs	https://doi.org/10.1039/b304443b
State	Published - 2003

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10.1039/b304443b

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title = "A facile tetrahydrothiophene-catalyzed ylide route to vinyloxiranes",

abstract = "Access to vinyloxiranes using aldehydes and allylic bromides in the presence of 1-5 mol% tetrahydrothiophene is reported. Both aliphatic and aromatic aldehydes work well in this reaction and the catalyst loading could be reduced as low as 0.5 mol%.",

author = "Kai Li and Deng, {Xian Ming} and Yong Tang",

year = "2003",

doi = "10.1039/b304443b",

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AU - Li, Kai

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N2 - Access to vinyloxiranes using aldehydes and allylic bromides in the presence of 1-5 mol% tetrahydrothiophene is reported. Both aliphatic and aromatic aldehydes work well in this reaction and the catalyst loading could be reduced as low as 0.5 mol%.

AB - Access to vinyloxiranes using aldehydes and allylic bromides in the presence of 1-5 mol% tetrahydrothiophene is reported. Both aliphatic and aromatic aldehydes work well in this reaction and the catalyst loading could be reduced as low as 0.5 mol%.

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U2 - 10.1039/b304443b

DO - 10.1039/b304443b

M3 - Article

AN - SCOPUS:0042066450

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JO - Chemical Communications

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A facile tetrahydrothiophene-catalyzed ylide route to vinyloxiranes

Abstract

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