Catalytic ethenylation reaction of phenol using SnCl4

Katsumi Kobayashi; Masahiko Yamaguchi

doi:10.1021/ol006888d

Catalytic ethenylation reaction of phenol using SnCl₄

Katsumi Kobayashi, Masahiko Yamaguchi

PHA - Molecular Pharmaceutical Science

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

18 Citations (Scopus)

Abstract

equation presented Ethenylation reaction of phenol with silylethyne at the o-position is catalyzed by the SnCl₄-BuLi reagent. While turn over numbers (TONs) in the reactions of m-or p-substituted phenols are 3 to 4, those for o-substituted phenols are 8 to 9.

Original language	English
Pages (from-to)	241-242
Number of pages	2
Journal	Organic letters
Volume	3
Issue number	2
DOIs	https://doi.org/10.1021/ol006888d
Publication status	Published - 2001 Jan 25

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/ol006888d

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title = "Catalytic ethenylation reaction of phenol using SnCl4",

abstract = "equation presented Ethenylation reaction of phenol with silylethyne at the o-position is catalyzed by the SnCl4-BuLi reagent. While turn over numbers (TONs) in the reactions of m-or p-substituted phenols are 3 to 4, those for o-substituted phenols are 8 to 9.",

author = "Katsumi Kobayashi and Masahiko Yamaguchi",

year = "2001",

month = jan,

day = "25",

doi = "10.1021/ol006888d",

language = "English",

volume = "3",

pages = "241--242",

journal = "Organic Letters",

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publisher = "American Chemical Society",

number = "2",

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T1 - Catalytic ethenylation reaction of phenol using SnCl4

AU - Kobayashi, Katsumi

AU - Yamaguchi, Masahiko

PY - 2001/1/25

Y1 - 2001/1/25

N2 - equation presented Ethenylation reaction of phenol with silylethyne at the o-position is catalyzed by the SnCl4-BuLi reagent. While turn over numbers (TONs) in the reactions of m-or p-substituted phenols are 3 to 4, those for o-substituted phenols are 8 to 9.

AB - equation presented Ethenylation reaction of phenol with silylethyne at the o-position is catalyzed by the SnCl4-BuLi reagent. While turn over numbers (TONs) in the reactions of m-or p-substituted phenols are 3 to 4, those for o-substituted phenols are 8 to 9.

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UR - http://www.scopus.com/inward/citedby.url?scp=0012687590&partnerID=8YFLogxK

U2 - 10.1021/ol006888d

DO - 10.1021/ol006888d

M3 - Article

C2 - 11430044

AN - SCOPUS:0012687590

SN - 1523-7060

VL - 3

SP - 241

EP - 242

JO - Organic Letters

JF - Organic Letters

IS - 2

ER -

Catalytic ethenylation reaction of phenol using SnCl₄

Abstract

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