A new Claisen sequence for the synthesis of 3-substituted-2-oxindoles

Kevin I. Booker-Milburn; Michael Fedouloff; Sandra J. Paknoham; John B. Strachan; James L. Melville; Martyn Voyle

A new Claisen sequence for the synthesis of 3-substituted-2-oxindoles

Kevin I. Booker-Milburn^*
, Michael Fedouloff
, Sandra J. Paknoham
, John B. Strachan
, James L. Melville
, Martyn Voyle

^*Corresponding author for this work

Research output: Contribution to journal › Article (Academic Journal) › peer-review

60 Citations (Scopus)

Abstract

Treatment of 3-methoxycarbonylindole with N-chlorosuccinimide followed by a range of alkenols yields 3-allylated-2-oxindoles in good yield, via a novel addition-Claisen rearrangement sequence. (C) 2000 Elsevier Science Ltd.

Translated title of the contribution	A New Claisen Sequence for the Synthesis of 3-Substituted-2-Oxindoles
Original language	English
Pages (from-to)	4657-4661
Number of pages	5
Journal	Tetrahedron Letters
Volume	41
Issue number	23
Publication status	Published - 12 Jun 2000

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@article{b45190d7b1014e93af0143ccfee88ffa,

title = "A new Claisen sequence for the synthesis of 3-substituted-2-oxindoles",

abstract = "Treatment of 3-methoxycarbonylindole with N-chlorosuccinimide followed by a range of alkenols yields 3-allylated-2-oxindoles in good yield, via a novel addition-Claisen rearrangement sequence. (C) 2000 Elsevier Science Ltd.",

author = "Booker-Milburn, \{Kevin I.\} and Michael Fedouloff and Paknoham, \{Sandra J.\} and Strachan, \{John B.\} and Melville, \{James L.\} and Martyn Voyle",

year = "2000",

month = jun,

day = "12",

language = "English",

volume = "41",

pages = "4657--4661",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "23",

}

TY - JOUR

T1 - A new Claisen sequence for the synthesis of 3-substituted-2-oxindoles

AU - Booker-Milburn, Kevin I.

AU - Fedouloff, Michael

AU - Paknoham, Sandra J.

AU - Strachan, John B.

AU - Melville, James L.

AU - Voyle, Martyn

PY - 2000/6/12

Y1 - 2000/6/12

N2 - Treatment of 3-methoxycarbonylindole with N-chlorosuccinimide followed by a range of alkenols yields 3-allylated-2-oxindoles in good yield, via a novel addition-Claisen rearrangement sequence. (C) 2000 Elsevier Science Ltd.

AB - Treatment of 3-methoxycarbonylindole with N-chlorosuccinimide followed by a range of alkenols yields 3-allylated-2-oxindoles in good yield, via a novel addition-Claisen rearrangement sequence. (C) 2000 Elsevier Science Ltd.

UR - https://www.scopus.com/pages/publications/0034640982

M3 - Article (Academic Journal)

SN - 0040-4039

VL - 41

SP - 4657

EP - 4661

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 23

ER -

A new Claisen sequence for the synthesis of 3-substituted-2-oxindoles

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