Syntheses of thiazole-containing macroheterocycles related to porphycene

The syntheses of 2,2′-bithiazole-containing and related expanded macrocycles 13 - 16 were accomplished by the McMurry coupling reaction of the corresponding [2,2′-bithiazole]-5,5′-dicarbaldehyde 6c and 2,2′-(1,4-phenylene)bis[thiazole-5-carbaldehyde] 7, readily available by a two-step reaction seque...

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Hauptverfasser: Nußbaumer, Thomas (VerfasserIn) , Neidlein, Richard (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 2000
In: Helvetica chimica acta
Year: 2000, Jahrgang: 83, Heft: 6, Pages: 1161-1167
ISSN:1522-2675
DOI:10.1002/1522-2675(20000607)83:6<1161::AID-HLCA1161>3.0.CO;2-2
Online-Zugang:Verlag, kostenfrei registrierungspflichtig, Volltext: http://dx.doi.org/10.1002/1522-2675(20000607)83:6<1161::AID-HLCA1161>3.0.CO;2-2
Verlag, kostenfrei registrierungspflichtig, Volltext: http://onlinelibrary.wiley.com/doi/10.1002/1522-2675(20000607)83:6<1161::AID-HLCA1161>3.0.CO;2-2/abstract
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Verfasserangaben:by Thomas Nussbaumer and Richard Neidlein
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Zusammenfassung:The syntheses of 2,2′-bithiazole-containing and related expanded macrocycles 13 - 16 were accomplished by the McMurry coupling reaction of the corresponding [2,2′-bithiazole]-5,5′-dicarbaldehyde 6c and 2,2′-(1,4-phenylene)bis[thiazole-5-carbaldehyde] 7, readily available by a two-step reaction sequence. The success of the dimerization strongly depends on the steric repulsion of the substituents vicinal to the CHO group.
Beschreibung:Gesehen am 28.04.2017
Beschreibung:Online Resource
ISSN:1522-2675
DOI:10.1002/1522-2675(20000607)83:6<1161::AID-HLCA1161>3.0.CO;2-2