0000000000563440

AUTHOR

Norbert Rumpf

showing 4 related works from this author

Monodisperse Oligo(2,5-dipropoxy-1,4-phenyleneethynylene)s

2002

Oligo(phenyleneethynylene)s 1 are rod-like compounds with undisturbed conjugation. In supplementation of the previously described members of this series 1a−e, with repeating units of up to n = 5, this work contains the preparation of higher oligomers 1f−i (n = 6, 7, 8, 10) through the use of the Sonogashira−Hagihara reaction. Both the absorption and the fluorescence bands showed convergence for increasing values of n, reaching limiting values at the effective conjugation length of nECL = 10. (© Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002)

ChemistryOrganic ChemistryDispersityPolymer chemistryLimitingPhysical and Theoretical ChemistryAbsorption (chemistry)Medicinal chemistryFluorescenceEuropean Journal of Organic Chemistry
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ChemInform Abstract: An Alternative Route to 2H-Naphtho[1,2-b]thiete and Its Cycloaddition Products.

2010

ChemistryOrganic chemistryGeneral MedicineCycloadditionChemInform
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An alternative route to 2H-naphtho[1,2-b]thiete and its cycloaddition products

1998

2-(1H-Benzotriazol-1-ylmethyl)-1-naphthalenol (1) can be transformed in high yields to the corresponding thiol 4. Flash vacuum pyrolysis of 4 leads to 2H-naphtho[1,2-b]thiete (5). The benzotriazolyl group proved to be a good leaving group; however, a subsequent nitrogen extrusion takes place under flash vacuum pyrolysis conditions and cyclopentadienecarbonitriles 6a,b are formed by a ring contraction (Scheme 1). Cycloaddition reactions of 5 and dienophiles or heterodienophiles yield the naphtho-condensed sulfur heterocycles 8, 10, 12 and 14 (Scheme 2).

chemistry.chemical_classificationchemistryFlash vacuum pyrolysisOrganic ChemistryThiolLeaving groupchemistry.chemical_elementSulfurMedicinal chemistryNitrogenCycloadditionJournal of Heterocyclic Chemistry
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Naphthothiete und ihre Anwendung in der Heterocyclen-Synthese

1995

Naphtothietes and Their Application to the Synthesis of Heterocycles The three isomeric naphthothietes 5, 11, and 16 were prepared according to the reaction sequences shown in Schemes 1–3. The final step was in each case a flash vacuum pyrolysis (FVP) of the corresponding mercaptonaphthalenemethanol 4, 9, and 15, respectively. The thiete rings in 5 and 11 can be opened by gentle heating; the ring opening of the isomer 16 possesses a much higher activation barrier. A MNDO calculation of the ΔHf values of 5, 11, and 16 and the open isomers 5′, 11′, and 16′ provides an explanation for the different behavior. Photochemical ring opening represents a useful alternative. The reaction Schemes 4, 6,…

chemistry.chemical_classificationDouble bondchemistryActivation barrierFlash vacuum pyrolysisStereochemistryOrganic ChemistryMNDOGeneral ChemistryPhysical and Theoretical ChemistryRing (chemistry)Medicinal chemistryCycloadditionLiebigs Annalen
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