Tricarbonylchromium complexes with methoxy substituted benzocyclobutenone and benzocyclobutenedione ligands

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Krishna Gopal Dongol
  • Jörn Krüger
  • Matthias Schnebel
  • Beate Voigt
  • Rudolf Wartchow
  • Holger Butenschön

Organisationseinheiten

Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Seiten (von - bis)150-157
Seitenumfang8
FachzeitschriftInorganica chimica acta
Jahrgang296
Ausgabenummer1
PublikationsstatusVeröffentlicht - 9 Dez. 1999

Abstract

The syntheses of methoxy substituted benzocyclobutenone and benzocyclobutenedione tricarbonylchromium complexes rac-4 and rac-10 are reported, rac-4 is preferentially obtained by a [2 + 2] cycloaddition of 3-methoxy-1,2-dehydrobenzene with diethoxyethene followed by complexation and acetal hydrolysis, whereas rac-10 is prepared by acetalization of the ligand followed by complexation and hydrolysis, rac-4 is stereoselectively reduced to the benzocyclobutenol complex with LiAlH4 in high yield. However, the anion driven ring opening-cycloaddition sequence furnished only poor selectivity. Vinyl Grignard addition to the 3-methoxybenzocyclobutenedione complex rac-10 gave the 1-vinyl adduct, which was characterized by an X-ray structure analysis.

ASJC Scopus Sachgebiete

Zitieren

Tricarbonylchromium complexes with methoxy substituted benzocyclobutenone and benzocyclobutenedione ligands. / Dongol, Krishna Gopal; Krüger, Jörn; Schnebel, Matthias et al.
in: Inorganica chimica acta, Jahrgang 296, Nr. 1, 09.12.1999, S. 150-157.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Dongol KG, Krüger J, Schnebel M, Voigt B, Wartchow R, Butenschön H. Tricarbonylchromium complexes with methoxy substituted benzocyclobutenone and benzocyclobutenedione ligands. Inorganica chimica acta. 1999 Dez 9;296(1):150-157. doi: 10.1016/s0020-1693(99)00353-9
Dongol, Krishna Gopal ; Krüger, Jörn ; Schnebel, Matthias et al. / Tricarbonylchromium complexes with methoxy substituted benzocyclobutenone and benzocyclobutenedione ligands. in: Inorganica chimica acta. 1999 ; Jahrgang 296, Nr. 1. S. 150-157.
Download
@article{542f55477cf6462dab65e93035ac1167,
title = "Tricarbonylchromium complexes with methoxy substituted benzocyclobutenone and benzocyclobutenedione ligands",
abstract = "The syntheses of methoxy substituted benzocyclobutenone and benzocyclobutenedione tricarbonylchromium complexes rac-4 and rac-10 are reported, rac-4 is preferentially obtained by a [2 + 2] cycloaddition of 3-methoxy-1,2-dehydrobenzene with diethoxyethene followed by complexation and acetal hydrolysis, whereas rac-10 is prepared by acetalization of the ligand followed by complexation and hydrolysis, rac-4 is stereoselectively reduced to the benzocyclobutenol complex with LiAlH4 in high yield. However, the anion driven ring opening-cycloaddition sequence furnished only poor selectivity. Vinyl Grignard addition to the 3-methoxybenzocyclobutenedione complex rac-10 gave the 1-vinyl adduct, which was characterized by an X-ray structure analysis.",
keywords = "Benzocyclobutenedione ligand, Benzocyclobutenone ligand, Crystal structures, Tricarbonylchromium complexes",
author = "Dongol, {Krishna Gopal} and J{\"o}rn Kr{\"u}ger and Matthias Schnebel and Beate Voigt and Rudolf Wartchow and Holger Butensch{\"o}n",
note = "Funding information: This work was generously supported by the Volkswagen-Stiftung and the Fonds der Chemischen Industrie. K.G. Dongol is indebted to the Gottlieb Daimler und Carl Benz-Stiftung for a doctoral fellowship. Donations of chemicals and solvents from BASF AG, Chemetall GmbH, Degussa-H{\"u}ls AG, and Phenolchemie GmbH are gratefully acknowledged.",
year = "1999",
month = dec,
day = "9",
doi = "10.1016/s0020-1693(99)00353-9",
language = "English",
volume = "296",
pages = "150--157",
journal = "Inorganica chimica acta",
issn = "0020-1693",
publisher = "Elsevier BV",
number = "1",

}

Download

TY - JOUR

T1 - Tricarbonylchromium complexes with methoxy substituted benzocyclobutenone and benzocyclobutenedione ligands

AU - Dongol, Krishna Gopal

AU - Krüger, Jörn

AU - Schnebel, Matthias

AU - Voigt, Beate

AU - Wartchow, Rudolf

AU - Butenschön, Holger

N1 - Funding information: This work was generously supported by the Volkswagen-Stiftung and the Fonds der Chemischen Industrie. K.G. Dongol is indebted to the Gottlieb Daimler und Carl Benz-Stiftung for a doctoral fellowship. Donations of chemicals and solvents from BASF AG, Chemetall GmbH, Degussa-Hüls AG, and Phenolchemie GmbH are gratefully acknowledged.

PY - 1999/12/9

Y1 - 1999/12/9

N2 - The syntheses of methoxy substituted benzocyclobutenone and benzocyclobutenedione tricarbonylchromium complexes rac-4 and rac-10 are reported, rac-4 is preferentially obtained by a [2 + 2] cycloaddition of 3-methoxy-1,2-dehydrobenzene with diethoxyethene followed by complexation and acetal hydrolysis, whereas rac-10 is prepared by acetalization of the ligand followed by complexation and hydrolysis, rac-4 is stereoselectively reduced to the benzocyclobutenol complex with LiAlH4 in high yield. However, the anion driven ring opening-cycloaddition sequence furnished only poor selectivity. Vinyl Grignard addition to the 3-methoxybenzocyclobutenedione complex rac-10 gave the 1-vinyl adduct, which was characterized by an X-ray structure analysis.

AB - The syntheses of methoxy substituted benzocyclobutenone and benzocyclobutenedione tricarbonylchromium complexes rac-4 and rac-10 are reported, rac-4 is preferentially obtained by a [2 + 2] cycloaddition of 3-methoxy-1,2-dehydrobenzene with diethoxyethene followed by complexation and acetal hydrolysis, whereas rac-10 is prepared by acetalization of the ligand followed by complexation and hydrolysis, rac-4 is stereoselectively reduced to the benzocyclobutenol complex with LiAlH4 in high yield. However, the anion driven ring opening-cycloaddition sequence furnished only poor selectivity. Vinyl Grignard addition to the 3-methoxybenzocyclobutenedione complex rac-10 gave the 1-vinyl adduct, which was characterized by an X-ray structure analysis.

KW - Benzocyclobutenedione ligand

KW - Benzocyclobutenone ligand

KW - Crystal structures

KW - Tricarbonylchromium complexes

UR - http://www.scopus.com/inward/record.url?scp=0000224071&partnerID=8YFLogxK

U2 - 10.1016/s0020-1693(99)00353-9

DO - 10.1016/s0020-1693(99)00353-9

M3 - Article

AN - SCOPUS:0000224071

VL - 296

SP - 150

EP - 157

JO - Inorganica chimica acta

JF - Inorganica chimica acta

SN - 0020-1693

IS - 1

ER -

Von denselben Autoren