New reactions of cyclic sulfoxides under Pummerer conditions

R A  Aitken; L  Hill; P  Lightfoot; Neil James Wilson

doi:10.1039/A904882K

New reactions of cyclic sulfoxides under Pummerer conditions

R A Aitken, L Hill, P Lightfoot, Neil James Wilson

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

Abstract

Reaction of the dihydrotetrathiafulvalene monosulfoxide 3 with TFAA results both in deoxygenation to give 1 and rearrangement to give the isomer 8, whose X-ray structure is presented; the corresponding disulfoxide 4 similarly rearranges to give 20.

Original language	English
Pages (from-to)	1673-1674
Number of pages	2
Journal	Chemical Communications
Issue number	17
DOIs	https://doi.org/10.1039/A904882K
Publication status	Published - 7 Sept 1999

Keywords

DIHYDROTETRATHIAFULVALENES

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title = "New reactions of cyclic sulfoxides under Pummerer conditions",

abstract = "Reaction of the dihydrotetrathiafulvalene monosulfoxide 3 with TFAA results both in deoxygenation to give 1 and rearrangement to give the isomer 8, whose X-ray structure is presented; the corresponding disulfoxide 4 similarly rearranges to give 20.",

keywords = "DIHYDROTETRATHIAFULVALENES",

author = "Aitken, {R A} and L Hill and P Lightfoot and Wilson, {Neil James}",

year = "1999",

month = sep,

day = "7",

doi = "10.1039/A904882K",

language = "English",

pages = "1673--1674",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

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T1 - New reactions of cyclic sulfoxides under Pummerer conditions

AU - Aitken, R A

AU - Hill, L

AU - Lightfoot, P

AU - Wilson, Neil James

PY - 1999/9/7

Y1 - 1999/9/7

N2 - Reaction of the dihydrotetrathiafulvalene monosulfoxide 3 with TFAA results both in deoxygenation to give 1 and rearrangement to give the isomer 8, whose X-ray structure is presented; the corresponding disulfoxide 4 similarly rearranges to give 20.

AB - Reaction of the dihydrotetrathiafulvalene monosulfoxide 3 with TFAA results both in deoxygenation to give 1 and rearrangement to give the isomer 8, whose X-ray structure is presented; the corresponding disulfoxide 4 similarly rearranges to give 20.

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U2 - 10.1039/A904882K

DO - 10.1039/A904882K

M3 - Article

SN - 1359-7345

SP - 1673

EP - 1674

JO - Chemical Communications

JF - Chemical Communications

IS - 17

ER -

New reactions of cyclic sulfoxides under Pummerer conditions

Abstract

Keywords

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