3-Hexanoyl-1-tosylindole. A highly stereospecific preparation of 3-alkyl-substituted indoles

Soad Mohialdin-Khaffaf; Krishna C. Persaud; Robin G. Pritchard

3-Hexanoyl-1-tosylindole. A highly stereospecific preparation of 3-alkyl-substituted indoles

Soad Mohialdin-Khaffaf, Krishna C. Persaud, Robin G. Pritchard

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

Abstract

The title molecule, 1-(1-tosyl-3-indolyl)-1-hexanone, C21H23NO3S, is configured so that the indole moiety eclipses one sulfonyl O atom and the toluene ring the other. As expected, the hexanoyl O atom is almost coplanar with the delocalized indole system.

Original language	English
Pages (from-to)	2607-2609
Number of pages	2
Journal	Acta Crystallographica Section C: Crystal Structure Communications
Volume	52
Issue number	10
Publication status	Published - 15 Oct 1996

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title = "3-Hexanoyl-1-tosylindole. A highly stereospecific preparation of 3-alkyl-substituted indoles",

abstract = "The title molecule, 1-(1-tosyl-3-indolyl)-1-hexanone, C21H23NO3S, is configured so that the indole moiety eclipses one sulfonyl O atom and the toluene ring the other. As expected, the hexanoyl O atom is almost coplanar with the delocalized indole system.",

author = "Soad Mohialdin-Khaffaf and Persaud, {Krishna C.} and Pritchard, {Robin G.}",

note = "Times Cited: 1 10",

year = "1996",

month = oct,

day = "15",

language = "English",

volume = "52",

pages = "2607--2609",

journal = "Acta Crystallographica Section C: Crystal Structure Communications",

issn = "0108-2701",

publisher = "International Union of Crystallography",

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TY - JOUR

T1 - 3-Hexanoyl-1-tosylindole. A highly stereospecific preparation of 3-alkyl-substituted indoles

AU - Mohialdin-Khaffaf, Soad

AU - Persaud, Krishna C.

AU - Pritchard, Robin G.

N1 - Times Cited: 1 10

PY - 1996/10/15

Y1 - 1996/10/15

N2 - The title molecule, 1-(1-tosyl-3-indolyl)-1-hexanone, C21H23NO3S, is configured so that the indole moiety eclipses one sulfonyl O atom and the toluene ring the other. As expected, the hexanoyl O atom is almost coplanar with the delocalized indole system.

AB - The title molecule, 1-(1-tosyl-3-indolyl)-1-hexanone, C21H23NO3S, is configured so that the indole moiety eclipses one sulfonyl O atom and the toluene ring the other. As expected, the hexanoyl O atom is almost coplanar with the delocalized indole system.

M3 - Article

SN - 0108-2701

VL - 52

SP - 2607

EP - 2609

JO - Acta Crystallographica Section C: Crystal Structure Communications

JF - Acta Crystallographica Section C: Crystal Structure Communications

IS - 10

ER -

3-Hexanoyl-1-tosylindole. A highly stereospecific preparation of 3-alkyl-substituted indoles

Abstract

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