Organic synthesis with α-chlorosulphides. Conversion of phenols into γ-lactones using methyl-2-chloro-2-(alkyl or arylthio)carboxylates

Michael Kennedy; Anita R. Maguire; M. Anthony McKervey

doi:10.1016/S0040-4039(00)84094-0

Organic synthesis with α-chlorosulphides. Conversion of phenols into γ-lactones using methyl-2-chloro-2-(alkyl or arylthio)carboxylates

Michael Kennedy
, Anita R. Maguire
, M. Anthony McKervey

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

Abstract

Aromatic γ-lactones can be synthesised from 4-substituted phenols in a single step by zinc chloride-catalysed alkylation with methyl-2-chloro-2-(butylthio or phenylthio)propionate or acetate.

Original language	English
Pages (from-to)	761-764
Number of pages	4
Journal	Tetrahedron Letters
Volume	27
Issue number	6
DOIs	https://doi.org/10.1016/S0040-4039(00)84094-0
Publication status	Published - 1986

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@article{839a26d8636345f589e10f6b92063ce3,

title = "Organic synthesis with α-chlorosulphides. Conversion of phenols into γ-lactones using methyl-2-chloro-2-(alkyl or arylthio)carboxylates",

abstract = "Aromatic γ-lactones can be synthesised from 4-substituted phenols in a single step by zinc chloride-catalysed alkylation with methyl-2-chloro-2-(butylthio or phenylthio)propionate or acetate.",

author = "Michael Kennedy and Maguire, \{Anita R.\} and McKervey, \{M. Anthony\}",

year = "1986",

doi = "10.1016/S0040-4039(00)84094-0",

language = "English",

volume = "27",

pages = "761--764",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Ltd",

number = "6",

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T1 - Organic synthesis with α-chlorosulphides. Conversion of phenols into γ-lactones using methyl-2-chloro-2-(alkyl or arylthio)carboxylates

AU - Kennedy, Michael

AU - Maguire, Anita R.

AU - McKervey, M. Anthony

PY - 1986

Y1 - 1986

N2 - Aromatic γ-lactones can be synthesised from 4-substituted phenols in a single step by zinc chloride-catalysed alkylation with methyl-2-chloro-2-(butylthio or phenylthio)propionate or acetate.

AB - Aromatic γ-lactones can be synthesised from 4-substituted phenols in a single step by zinc chloride-catalysed alkylation with methyl-2-chloro-2-(butylthio or phenylthio)propionate or acetate.

UR - https://www.scopus.com/pages/publications/85004254081

U2 - 10.1016/S0040-4039(00)84094-0

DO - 10.1016/S0040-4039(00)84094-0

M3 - Article

AN - SCOPUS:85004254081

SN - 0040-4039

VL - 27

SP - 761

EP - 764

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 6

ER -

Organic synthesis with α-chlorosulphides. Conversion of phenols into γ-lactones using methyl-2-chloro-2-(alkyl or arylthio)carboxylates

Abstract

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