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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 113 (1982), S. 781-792 
    ISSN: 1434-4475
    Keywords: Active methylene group ; Ketone ; 1,2,4-Oxadiazole ; Vinyl dimethylcarbamate ; 5-Vinyl-oxadiazole
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Aliphatic amidoximesR—C (NH2)=NOH react with diketene to yield 5-acetonyl-3-alkyl-1,2,4-oxadiazoles, which are susceptible to a wide variety of reactions at the keto-group as well as at the methylene-group. Their transformations into 1-methyl-2-oxadiazolyl-vinylN,N-dimethylcarbamates, 2-chloro-1-oxadiazolylpropenes, 1-oxadiazolyl-2-(1,2,4-triazol-1-yl)propenes, 1,1-dichloro-1-oxadiazolylacetones and 3-hydroxy-2-oxadiazolyl-crotonic amides are described as well as their reactions with diazonium salts, with sodium nitrite and with carbon disulfide. Further products obtained are carbamates of of 1-oxadiazolyl-2-oxo-propane-1-oximes, 2-chloro-2-oxadiazolylvinyl phosphates and an oxadiazolyl pyrimidine.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 113 (1982), S. 793-803 
    ISSN: 1434-4475
    Keywords: Ketone ; 1,2,4-Oxadiazole ; 1,3,4-Oxadiazole ; 1,2,4-Thiadiazole ; Vinyl phosphate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract 3-Acetonyl-1,2,4-oxadiazoles and 2-acetonyl-1,3,4-oxadiazoles are accessible starting with the ketal of acetoacetamide oxime and the ketal of acetoacetic acid hydrazide, respectively. 5-Acetonyl-1,2,4-thiadiazoles are obtained from 5-chloro-1,2,4-thiadiazoles andtert.-butyl acetoacetate. These Acetonyl-azoles are starting materials for three series of azolylvinyl phosphates and phosphonates.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 114 (1983), S. 373-376 
    ISSN: 1434-4475
    Keywords: Enolate ; Isoxazole ; Ketone ; Mononuclear rearrangement ; 1,2,4-Oxadiazole
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract 3-Acetonyl-1,2,4-oxadiazoles on treatment with strong bases rearrange via their enolates by simultaneous cleavage of one N-O-bond and forming of another N-O-bond to 3-acylamino-isoxazoles.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1980 (1980), S. 1392-1401 
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Simple Synthesis of 4-(Heteroarylmethyl)phenols and Their AcylationCondensation of 4-hydroxybenzaldehyde (1) with ethyl acetoacetate (2a) or acetylacetone (2b) gives 3a and 3b, respectively, which on hydrogenation afford the 2-(4-hydroxybenzyl)-1,3-dicarbonyl compounds 4a and 4b, respectively. These react with hydrazines or hydroxylamine to give the 4-(4-pyrazolylmethyl)phenols 5 and the 4-(4-isoxazolylmethyl)phenol 6, respectively. Reaction of 4a with acetamidine affords 5-(4-hydroxybenzyl)-2,6-dimethyl-4-pyrimidinol (7a). On acylation with methyl isocyanate, 5a and 7a are esterified at the phenolic hydroxy group, whereas acyl chlorides react at the pyrazole OH group. In the case of 4-(3,5-dimethyl-4-pyrazolyl-methyl)phenol (5a) priority of O- or N-acylation depends on the base used.
    Notes: 4-Hydroxybenzaldehyd (1) wird mit Acetessigester (2a) oder Acetylaceton (2b) zu 3a bzw. 3b kondensiert, die zu den 2-(4-Hydroxybenzyl)-1,3-dicarbonylverbindungen 4a bzw. 4b hydriert werden. Diese liefern mit Hydrazinen oder Hydroxylamin die 4-(4-Pyazolylmethyl)phenole 5 bzw. das 4-(4-Isoxazolylmethyl)phenol 6. Aus 4a und Acetamidin wird 5-(4-Hydroxybenzyl)-2,6-dimethyl-4-pyrimidinol (7a) erhalten. Bei der Acylierung mit Methylisocyanat reagieren 5 sowie 7a unter Veresterung der phenolischen Hydroxygruppe. Säurechloride verestern dagegen die Pyrazol-OH-Gruppe. Beim 4-(3,5-Dimethyl-4-pyrazolylmethyl)phenol (5a) hängt der Vorrang von O- oder N-Acylierung von der eingesetzten Base ab.
    Additional Material: 2 Tab.
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  • 5
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Heterocycles by Annelation to 4-Pyridinols, III1)  -  2-Aminopyrido[3,4-e][1,3]thiazin-4-onesHerrn Prof. Dr. Rolf Sammet zum 60. Geburtstag gewidmet.2-Aminopyrido[3,4-e][1,3]thiazin-4-ones 4 are obtained from 4-hydroxy-3-pyridinecarboxylic esters 1 via 4-chloro-3-pyridinecarboxylic esters 2 and reaction of the latter ones with thiourea. The 1,3-thiazin-4-one ring in 4 is very easily cleaved by alkali to give acylureas 5. Carboxylic chlorides and isocyanates react with compounds 4 at the thiazinone ring nitrogen to yield 3-acylpyrido[3,4-e]thiazinones 7, the structure of which is deduced from mass spectra. On the other hand chloroformic acid derivatives in N,N-dimethylformamide attack the exocyclic nitrogen to transform 4a into the dimethylformamidine 9.
    Notes: 2-Aminopyrido[3,4-e][1,3]thiazin-4-one 4 werden aus 4-Hydroxy-3-pyridincarbonsäureestern 1 über 4-Chlor-3-pyridincarbonsäureester 2 mit Thioharnstoff erhalten. 1,3-Thiazin-4-one 4 werden durch Alkali sehr leicht zu Acylharnstoffen 5 gespalten. Mit Carbonsäurechloriden und mit Isocyanaten reagieren die Verbindungen 4 am Thiazinonring-Stickstoff zu 3-Acylpyrido[3,4-e]-thiazinonen 7, deren Struktur aus den Massenspektren abgeleitet wird. Chlorameisensäurederivate in N,N-Dimethylformamid überführen dagegen 4a unter Angriff auf den exocyclischen Stickstoff in das Dimethylformamidin 9.
    Additional Material: 2 Tab.
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