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Über die Bildung von 1,1,2,3-Tetrachlor-2,3-diethoxycyclopropan bei phasentransferkatalysierten Dichlorcyclopropanierungen.

Research output: Journal contributions › Comments / Debate / Reports › Research

Standard

Über die Bildung von 1,1,2,3-Tetrachlor-2,3-diethoxycyclopropan bei phasentransferkatalysierten Dichlorcyclopropanierungen. / Rücker, Christoph.
In: Chemische Berichte, Vol. 118, No. 5, 01.05.1985, p. 2137-2139.

Research output: Journal contributions › Comments / Debate / Reports › Research

Harvard

Rücker, C 1985, 'Über die Bildung von 1,1,2,3-Tetrachlor-2,3-diethoxycyclopropan bei phasentransferkatalysierten Dichlorcyclopropanierungen.', Chemische Berichte, vol. 118, no. 5, pp. 2137-2139. https://doi.org/10.1002/cber.19851180534

APA

Rücker, C. (1985). Über die Bildung von 1,1,2,3-Tetrachlor-2,3-diethoxycyclopropan bei phasentransferkatalysierten Dichlorcyclopropanierungen. Chemische Berichte, 118(5), 2137-2139. https://doi.org/10.1002/cber.19851180534

Vancouver

Rücker C. Über die Bildung von 1,1,2,3-Tetrachlor-2,3-diethoxycyclopropan bei phasentransferkatalysierten Dichlorcyclopropanierungen. Chemische Berichte. 1985 May 1;118(5):2137-2139. doi: 10.1002/cber.19851180534

Bibtex

@article{3105e74112b945a08e722edbc9750dc5,
title = "{\"U}ber die Bildung von 1,1,2,3-Tetrachlor-2,3-diethoxycyclopropan bei phasentransferkatalysierten Dichlorcyclopropanierungen.",
abstract = "On the Formation of 1,1,2,3‐Tetrachloro‐2,3‐diethoxycyclopropane in Phase Transfer Catalysed Dichlorocyclopropanations When phase transfer catalysed dichlorocyclopropanations are performed in commercial chloroform as reagent/solvent (50% aq. NaOH/TEBA‐Cl, 40°C), the title compound 4 (a single stereoisomer assumed to be trans) is produced from the ethanol present in chloroform as a stabiliser. Formation of 4 can be avoided by pre‐extracting the chloroform with water. A reaction path for the formation of 4 is proposed. Copyright {\textcopyright} 1985 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim",
keywords = "Chemie",
author = "Christoph R{\"u}cker",
year = "1985",
month = may,
day = "1",
doi = "10.1002/cber.19851180534",
language = "Deutsch",
volume = "118",
pages = "2137--2139",
journal = "Chemische Berichte",
issn = "0009-2940",
publisher = "John Wiley & Sons Ltd.",
number = "5",

}

RIS

TY - JOUR

T1 - Über die Bildung von 1,1,2,3-Tetrachlor-2,3-diethoxycyclopropan bei phasentransferkatalysierten Dichlorcyclopropanierungen.

AU - Rücker, Christoph

PY - 1985/5/1

Y1 - 1985/5/1

N2 - On the Formation of 1,1,2,3‐Tetrachloro‐2,3‐diethoxycyclopropane in Phase Transfer Catalysed Dichlorocyclopropanations When phase transfer catalysed dichlorocyclopropanations are performed in commercial chloroform as reagent/solvent (50% aq. NaOH/TEBA‐Cl, 40°C), the title compound 4 (a single stereoisomer assumed to be trans) is produced from the ethanol present in chloroform as a stabiliser. Formation of 4 can be avoided by pre‐extracting the chloroform with water. A reaction path for the formation of 4 is proposed. Copyright © 1985 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim

AB - On the Formation of 1,1,2,3‐Tetrachloro‐2,3‐diethoxycyclopropane in Phase Transfer Catalysed Dichlorocyclopropanations When phase transfer catalysed dichlorocyclopropanations are performed in commercial chloroform as reagent/solvent (50% aq. NaOH/TEBA‐Cl, 40°C), the title compound 4 (a single stereoisomer assumed to be trans) is produced from the ethanol present in chloroform as a stabiliser. Formation of 4 can be avoided by pre‐extracting the chloroform with water. A reaction path for the formation of 4 is proposed. Copyright © 1985 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim

KW - Chemie

UR - http://www.scopus.com/inward/record.url?scp=84942720507&partnerID=8YFLogxK

UR - https://www.mendeley.com/catalogue/b7a037bf-132d-34a9-a48a-a21bbd3ff321/

U2 - 10.1002/cber.19851180534

DO - 10.1002/cber.19851180534

M3 - Kommentare / Debatten / Berichte

VL - 118

SP - 2137

EP - 2139

JO - Chemische Berichte

JF - Chemische Berichte

SN - 0009-2940

IS - 5

ER -

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Research output: Journal contributions › Journal articles › Research › peer-review

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Research output: Journal contributions › Journal articles › Research › peer-review

Other publications by the same author(s)

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Research output: Journal contributions › Journal articles › Research › peer-review

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Research output: Journal contributions › Journal articles › Research › peer-review

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Research output: Working paper › Project reports › Research

Comment on "nomenclature, Chemical Abstracts Service Numbers, Isomer Enumeration, Ring Strain, and Stereochemistry: What Does Any of This Have to Do with an International Chemical Disarmament and Nonproliferation Treaty?"

Rücker, C., Meringer, M. & Wassermann, A., 13.04.2021, In: Journal of Chemical Education. 98, 4, p. 1465-1467 3 p.

Research output: Journal contributions › Comments / Debate / Reports › Research

Octanol-Water Partition Coefficient Measurement by a Simple 1H NMR Method

Cumming, H. & Rücker, C., 30.09.2017, In: ACS Omega. 2, 9, p. 6244-6249 6 p.

Research output: Journal contributions › Journal articles › Research › peer-review

DOI

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