Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Andrés Villalpando"'
Publikováno v:
Acta Crystallographica Section E, Vol 66, Iss 6, Pp o1353-o1353 (2010)
The title compound, C22H17NO, is a novel Schiff base synthesized via a condensation reaction between 9-anthracenecarboxaldehyde and 2-amino-p-cresol. The asymmetric unit contains two independent molecules that are joined by an O—H...OH hydrogen bon
Externí odkaz:
https://doaj.org/article/1240cee9d0d447d5a41eb40f1fd6b986
Publikováno v:
Chemical Communications. 51:15075-15078
We describe a strategy to chlorinate stereocomplementary acyclic aliphatic 1,3-diols using a mixture of triphosgene and pyridine. While 1,3-anti diols readily led to 1,3-anti dichlorides, 1,3-syn diols must be converted to 1,3-syn diol monosilylether
Publikováno v:
Organic Letters. 14:3676-3679
Activation of primary aliphatic alcohols with triphosgene and triethylamine mixtures afforded either alkyl chloride or diethylcarbamate products, and the switch in selectivity appeared to be driven by sterics. The reaction conditions to achieve this
Publikováno v:
Journal of Chemical Crystallography. 41:1342-1347
The Schiff base 2-(9-anthrylmethylideneamino)-5-methylphenol has been prepared in good yield (55%) from commercially available starting materials. The photophysical properties of this compound and its precursor have been determined. The room temperat
Publikováno v:
The Journal of organic chemistry. 78(8)
Unactivated α-branched primary and secondary aliphatic alcohols have been successfully transformed into their corresponding alkyl chlorides in high yields upon treatment with a mixture of triphosgene and pyridine in dichloromethane at reflux. These
Publikováno v:
ChemInform. 43
Diols bearing a primary and a tertiary hydroxyl group such as (Ia) and (Ib) are selectively chlorinated at the primary function.
The synthesis, X-ray structure analysis, and photophysical characterization of 3,3′-diacetylstilbene
Publikováno v:
Journal of Molecular Structure.
3,3′-Diacetylstilbene was produced in modest yield (26%) from a palladium(II) acetate-catalyzed coupling reaction between triethoxyvinylsilane and the triazene 1-{3-[(E)-morpholin-4-yldiazenyl]phenyl}ethanone. X-ray analysis of crystals of 3,3′-d
Publikováno v:
Acta Crystallographica Section E, Vol 66, Iss 6, Pp o1353-o1353 (2010)
Acta Crystallographica Section E: Structure Reports
Acta Crystallographica Section E: Structure Reports
The title compound, C22H17NO, is a novel Schiff base synthesized via a condensation reaction between 9-anthracenecarboxaldehyde and 2-amino-p-cresol. The asymmetric unit contains two independent molecules that are joined by an O—H...OH hydrogen bon