Friedel-Crafts alkylation of benzene and toluene with olefinic C-6 hydrocarbons and esters

KD Black; FD Gunstone

doi:10.1016/0009-3084(95)02517-0

Friedel-Crafts alkylation of benzene and toluene with olefinic C-6 hydrocarbons and esters

KD Black
, FD Gunstone

SAMS UHI

Producción científica: Article › revisión exhaustiva

4 Citas (Scopus)

Resumen

To assist our study of the reaction of toluene and other aromatic compounds with methyl oleate and other olefinic esters, benzene and toluene have been alkylated under Friedel-Crafts conditions with hex-1-ene, hex-3-ene, methyl hex-3-enoate and methyl hex-3-enedioate. The products were isolated and identified by NMR and mass spectrometric procedures.

Idioma original	English
Páginas (desde-hasta)	79-86
Número de páginas	8
Publicación	Chemistry and Physics of Lipids
Volumen	79
N.º	1
DOI	https://doi.org/10.1016/0009-3084(95)02517-0
Estado	Published - 25 ene 1996

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@article{c93600f8a610482eb467240dc5b3ca54,

title = "Friedel-Crafts alkylation of benzene and toluene with olefinic C-6 hydrocarbons and esters",

abstract = "To assist our study of the reaction of toluene and other aromatic compounds with methyl oleate and other olefinic esters, benzene and toluene have been alkylated under Friedel-Crafts conditions with hex-1-ene, hex-3-ene, methyl hex-3-enoate and methyl hex-3-enedioate. The products were isolated and identified by NMR and mass spectrometric procedures.",

author = "KD Black and FD Gunstone",

year = "1996",

month = jan,

day = "25",

doi = "10.1016/0009-3084(95)02517-0",

language = "English",

volume = "79",

pages = "79--86",

journal = "Chemistry and Physics of Lipids",

issn = "0009-3084",

publisher = "Elsevier Ireland Ltd",

number = "1",

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TY - JOUR

T1 - Friedel-Crafts alkylation of benzene and toluene with olefinic C-6 hydrocarbons and esters

AU - Black, KD

AU - Gunstone, FD

PY - 1996/1/25

Y1 - 1996/1/25

N2 - To assist our study of the reaction of toluene and other aromatic compounds with methyl oleate and other olefinic esters, benzene and toluene have been alkylated under Friedel-Crafts conditions with hex-1-ene, hex-3-ene, methyl hex-3-enoate and methyl hex-3-enedioate. The products were isolated and identified by NMR and mass spectrometric procedures.

AB - To assist our study of the reaction of toluene and other aromatic compounds with methyl oleate and other olefinic esters, benzene and toluene have been alkylated under Friedel-Crafts conditions with hex-1-ene, hex-3-ene, methyl hex-3-enoate and methyl hex-3-enedioate. The products were isolated and identified by NMR and mass spectrometric procedures.

U2 - 10.1016/0009-3084(95)02517-0

DO - 10.1016/0009-3084(95)02517-0

M3 - Article

SN - 0009-3084

VL - 79

SP - 79

EP - 86

JO - Chemistry and Physics of Lipids

JF - Chemistry and Physics of Lipids

IS - 1

ER -

Friedel-Crafts alkylation of benzene and toluene with olefinic C-6 hydrocarbons and esters

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