Pseudo-geminally-substituted [2.2]paracyclophanes as spacers for bisallenyl sulfoxides and sulfones

M. Lucian Birsa; Peter G. Jones; Samuel Braverman; Henning Hopf

doi:10.1055/s-2005-863715

Pseudo-geminally-substituted [2.2]paracyclophanes as spacers for bisallenyl sulfoxides and sulfones

M. Lucian Birsa, Peter G. Jones, Samuel Braverman, Henning Hopf

Department of Chemistry

Technical University of Braunschweig

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

2 Scopus citations

Abstract

The first pseudo-geminally-substituted bisallenic [2.2]paracyclophane system has been synthesized by the [2,3]sigmatropic rearrangement of propargylic sulfenates to the corresponding allenyl sulfoxides.

Original language	English
Pages (from-to)	640-642
Number of pages	3
Journal	Synlett
Issue number	4
DOIs	https://doi.org/10.1055/s-2005-863715
State	Published - 4 Mar 2005

Keywords

Allenes
Sigmatropic rearrangements
Sulfenates
Sulfones
[2.2]paracyclophanes

Access to Document

10.1055/s-2005-863715

Cite this

@article{3188d74410e249cab09256d1c9f82033,

title = "Pseudo-geminally-substituted [2.2]paracyclophanes as spacers for bisallenyl sulfoxides and sulfones",

abstract = "The first pseudo-geminally-substituted bisallenic [2.2]paracyclophane system has been synthesized by the [2,3]sigmatropic rearrangement of propargylic sulfenates to the corresponding allenyl sulfoxides.",

keywords = "Allenes, Sigmatropic rearrangements, Sulfenates, Sulfones, [2.2]paracyclophanes",

author = "{Lucian Birsa}, M. and Jones, {Peter G.} and Samuel Braverman and Henning Hopf",

year = "2005",

month = mar,

day = "4",

doi = "10.1055/s-2005-863715",

language = "אנגלית",

pages = "640--642",

journal = "Synlett",

issn = "0936-5214",

publisher = "Georg Thieme Verlag",

number = "4",

}

TY - JOUR

T1 - Pseudo-geminally-substituted [2.2]paracyclophanes as spacers for bisallenyl sulfoxides and sulfones

AU - Lucian Birsa, M.

AU - Jones, Peter G.

AU - Braverman, Samuel

AU - Hopf, Henning

PY - 2005/3/4

Y1 - 2005/3/4

N2 - The first pseudo-geminally-substituted bisallenic [2.2]paracyclophane system has been synthesized by the [2,3]sigmatropic rearrangement of propargylic sulfenates to the corresponding allenyl sulfoxides.

AB - The first pseudo-geminally-substituted bisallenic [2.2]paracyclophane system has been synthesized by the [2,3]sigmatropic rearrangement of propargylic sulfenates to the corresponding allenyl sulfoxides.

KW - Allenes

KW - Sigmatropic rearrangements

KW - Sulfenates

KW - Sulfones

KW - [2.2]paracyclophanes

UR - http://www.scopus.com/inward/record.url?scp=15544362423&partnerID=8YFLogxK

U2 - 10.1055/s-2005-863715

DO - 10.1055/s-2005-863715

M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???

AN - SCOPUS:15544362423

SN - 0936-5214

SP - 640

EP - 642

JO - Synlett

JF - Synlett

IS - 4

ER -

Pseudo-geminally-substituted [2.2]paracyclophanes as spacers for bisallenyl sulfoxides and sulfones

Abstract

Keywords

Access to Document

Other files and links

Fingerprint

Cite this