Preparation and NMR spectra of four isomeric diformyl[2.2]paracyclophanes (cyclophanes 66)

Four isomeric dialdehydes 4, readily available from cycloaddition of propiolic aldehyde (2) to 1,2,4,5-hexatetraene (1), were separated by chromatography and recrystallization, and were characterized by their spectroscopic data. The individual isomers can now be easily identified from their 1H NMR s...

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Main Authors: Ina Dix, Henning Hopf, Thota B. N. Satyanarayana, Ludger Ernst
Format: Article
Language:English
Published: Beilstein-Institut 2010-09-01
Series:Beilstein Journal of Organic Chemistry
Subjects:
Online Access:https://doi.org/10.3762/bjoc.6.104
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author Ina Dix
Henning Hopf
Thota B. N. Satyanarayana
Ludger Ernst
author_facet Ina Dix
Henning Hopf
Thota B. N. Satyanarayana
Ludger Ernst
author_sort Ina Dix
collection DOAJ
description Four isomeric dialdehydes 4, readily available from cycloaddition of propiolic aldehyde (2) to 1,2,4,5-hexatetraene (1), were separated by chromatography and recrystallization, and were characterized by their spectroscopic data. The individual isomers can now be easily identified from their 1H NMR spectra even if only one of them is present.
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spelling doaj.art-c9e7848249f0492e8bca68a964aab7ca2022-12-21T22:50:05ZengBeilstein-InstitutBeilstein Journal of Organic Chemistry1860-53972010-09-016193293710.3762/bjoc.6.1041860-5397-6-104Preparation and NMR spectra of four isomeric diformyl[2.2]paracyclophanes (cyclophanes 66)Ina Dix0Henning Hopf1Thota B. N. Satyanarayana2Ludger Ernst3Institut für Organische Chemie, Technische Universität Braunschweig, Hagenring 30, D-38106 Braunschweig, GermanyInstitut für Organische Chemie, Technische Universität Braunschweig, Hagenring 30, D-38106 Braunschweig, GermanyInstitut für Organische Chemie, Technische Universität Braunschweig, Hagenring 30, D-38106 Braunschweig, GermanyNMR-Laboratorium der Chemischen Institute, Technische Universität Braunschweig, Hagenring 30, D-38106 Braunschweig, GermanyFour isomeric dialdehydes 4, readily available from cycloaddition of propiolic aldehyde (2) to 1,2,4,5-hexatetraene (1), were separated by chromatography and recrystallization, and were characterized by their spectroscopic data. The individual isomers can now be easily identified from their 1H NMR spectra even if only one of them is present.https://doi.org/10.3762/bjoc.6.104cyclophanesdiformyl[2.2]paracyclophaneslayered compoundsNMR spectroscopystructure assignment
spellingShingle Ina Dix
Henning Hopf
Thota B. N. Satyanarayana
Ludger Ernst
Preparation and NMR spectra of four isomeric diformyl[2.2]paracyclophanes (cyclophanes 66)
Beilstein Journal of Organic Chemistry
cyclophanes
diformyl[2.2]paracyclophanes
layered compounds
NMR spectroscopy
structure assignment
title Preparation and NMR spectra of four isomeric diformyl[2.2]paracyclophanes (cyclophanes 66)
title_full Preparation and NMR spectra of four isomeric diformyl[2.2]paracyclophanes (cyclophanes 66)
title_fullStr Preparation and NMR spectra of four isomeric diformyl[2.2]paracyclophanes (cyclophanes 66)
title_full_unstemmed Preparation and NMR spectra of four isomeric diformyl[2.2]paracyclophanes (cyclophanes 66)
title_short Preparation and NMR spectra of four isomeric diformyl[2.2]paracyclophanes (cyclophanes 66)
title_sort preparation and nmr spectra of four isomeric diformyl 2 2 paracyclophanes cyclophanes 66
topic cyclophanes
diformyl[2.2]paracyclophanes
layered compounds
NMR spectroscopy
structure assignment
url https://doi.org/10.3762/bjoc.6.104
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