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

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

29 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
Externally published	Yes

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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",

language = "English",

volume = "3",

pages = "2074--2075",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "16",

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TY - JOUR

T1 - A facile tetrahydrothiophene-catalyzed ylide route to vinyloxiranes

AU - Li, Kai

AU - Deng, Xian Ming

AU - Tang, Yong

PY - 2003

Y1 - 2003

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%.

UR - https://www.scopus.com/pages/publications/0042066450

U2 - 10.1039/b304443b

DO - 10.1039/b304443b

M3 - Article

AN - SCOPUS:0042066450

SN - 1359-7345

VL - 3

SP - 2074

EP - 2075

JO - Chemical Communications

JF - Chemical Communications

IS - 16

ER -

A facile tetrahydrothiophene-catalyzed ylide route to vinyloxiranes

Abstract

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