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  • 1970-1974  (13)
  • 1955-1959
  • 1940-1944
  • 1935-1939
  • 1973  (4)
  • 1970  (9)
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  • 1970-1974  (13)
  • 1955-1959
  • 1940-1944
  • 1935-1939
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  • 1
    Electronic Resource
    Electronic Resource
    Orthoamide, X Reaktionen vinyloger Amidacetale, Aminalester und Amidaminale (1970)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 103 (1970), S. 222-235 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Orthoamides, X: Reaction of Vinylogous Amide Acetals, Aminalesters and Amide AminalsDerivates of vinylogous orthoformic acid amides react with Grignard compounds to give l,3-bis(dimethylamino)-l-alkenes (4-7), with methylene active compounds to give derivates of N.N-disubstituted 4-amino-l,3-butadienes (17  - 29) and with primary aromatic amines to form vinylogous, N,N,N′-trisubstituted amidines (31-36, 38-40).
    Notes: Vinyloge Orthoameisensäureamid-Derivate geben mit Grignard-Verbindungen 1.3-Bis - dimethylamino-alkene-(l) (4-7), mit methylenaktiven Verbindungen N.N-disubstituierte 4 - Amino-butadien-(l.3)-Derivate (17-29) und mit primären aromatischen Aminen vinyloge N.N.N′-trisubstituierte Amidine (31-36, 38-40).
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19701030130
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  • 2
    Electronic Resource
    Electronic Resource
    Orthoamide, XII Synthese von O.N- bzw. N.N-Acetalen der Acylisocyanate aus Amidacetalen bzw. einem Aminal-tert.-butylester und N-Halogen-carbonsäureamiden, Halogenharnstoffen und N-Chlor-urethan (1970)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 103 (1970), S. 245-255 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Orthoamides, XII: Synthesis of Acyl Isocyanate O,N- or -N,N-Acetals from Amide Acetals or from an Aminal tert-Butylester and N-Halogencarbonamides, Halogen Ureas and N-ChlorourethanesDimethylformamide dialkylacetals (2) and aminal-tert-butylester 5 [bis(dimethylamino)-tert-butoxymethane] react with N-halogen carboxylic acid amides, halogen ureas and N-chlorourethanes to give acyl isocyanate-O,N -or -N,N-acetals (isoureas 3 or guanidines 6, respectively).
    Notes: Dimethylformamid-dialkylacetale (2) und Aminal-tert.-butylester 5 (Bis-dimethylamino-tert.-butyloxy-methan) bilden mit N-Halogen-carbonsäureamiden, Halogenharnstoffen und N-Chlor-urethan Acylisocyanat-O.N- bzw. -N.N-acetale (Isoharnstoffe 3 bzw. Guanidine 6).
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19701030132
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  • 3
    Electronic Resource
    Electronic Resource
    Orthoamide, XIII Untersuchungen zum Reaktionsmechanismus der elektrophilen Substitution des Formyl-H-Atoms bei Orthoameisensäureamid-Derivaten (1970)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 103 (1970), S. 256-264 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Orthoamides, XIII Studies on the Mechanism of Electrophilic Substitution of the Formyl-H Atom in Ortho Formic Acid AmidesOrtho formic acid amides and N-halogen carboxylic acid amides, halogen ureas or N-chloro urethanes primarily react to give adducts; these form ylides in the presence of bases. The ylides react by an intramolecular SE1- or SNi-mechanism to give O,N-acetals of the corresponding acyl isocyanates (isoureas).
    Notes: Bei der Umsetzung von Orthoamiden mit N-Halogen-carbonsäureamiden, -harnstoffen und N-Chlor-urethan wurden Primär-Addukte nachgewiesen. Diese bilden in Gegenwart von Basen Ylide, welche über einen intramolekularen SE1- oder SNi-Mechanismus C-N-Knüpfung eingehen unter Bildung von O.N-Acetalen der entsprechenden Acylisocyanate (Isoharnstoffe).
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19701030133
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  • 4
    Electronic Resource
    Electronic Resource
    Orthoamide, XXIV. Synthese und Reaktionen von Amidthioacetalen und Aminalthioestern (1973)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 106 (1973), S. 3725-3731 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Orthoamides, XXIV. Synthesis and Reactions of Amide Thioacetals and Aminal ThioestersThe amide thioacetals 2 are obtained by reaction of the N,N-dimethylformamide dimethyl sulfate adduct 1 with sodium thiolates or by treatment of N,N-dimethylformamide diethyl acetal (3) with alkanthiols. Aminal thioesters 11 are formed by reaction of tetramethylformamidinium methyl sulfate (10) with alkali alkanethiolates or by treatment of aminal-tert-butylester 12 with alkanethiols. The compounds have properties similar to those of their oxygen homologues.
    Notes: Amidthioacetale 2 erhält man aus dem N,N-Dimethylformamid-Dimethylsulfat-Addukt 1 und Natriumthiolaten oder aus N,N-Dimethylformamid-diäthylacetal (3) und Alkanthiolen, Aminalthioester 11 aus Tetramethylformamidinium-methylsulfat (10) und Alkali-alkanthiolaten oder aus dem Aminal-tert-butylester 12 und Alkanthiolen. Die Verbindungen zeigen ähnliche Eigenschaften wie ihre Sauerstoff-Homologen.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19731061131
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  • 5
    Electronic Resource
    Electronic Resource
    Orthoamide, XI Umsetzungen von Dimethylformamid-dialkylacetalen mit Isocyanaten (1970)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 103 (1970), S. 236-244 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Orthoamides, XI Reactions of Dimethylformamide Dialkyl Acetals with IsocyanatesDimethylformamide dialkyl acetals react with aliphatic and aromatic isocyanates to give parabanic acid O,N-acetals (= 1,3-disubstituted 5-dimethylamino-5-alkoxy-2,4-dioxoimidazolidines) (1). It is likely that an ylide is formed as an intermediate, as shown by reactions.
    Notes: Bei der Umsetzung von Dimethylformamid-dialkylacetalen mit aliphatischen und aromatischen Isocyanaten entstehen Parabansäure-O.N-acetale (= 1.3-disubstituierte 5-Dimethylamino-5-alkoxy-2.4-dioxo-imidazolidine) (1). Die Bildung eines Ylids als Zwischenprodukt konnte wahrscheinlich gemacht werden.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19701030131
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  • 6
    Electronic Resource
    Electronic Resource
    Orthoamide, XXV. Synthese und Reaktionen von [α-(Dimethylaminomethylen)-benzyl]triphenylphosphonium-Salzen (1973)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 106 (1973), S. 3732-3742 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Orthoamides, XXV. Synthesis and Reactions of [α-(Dimethylaminomethylene)benzyl]triphenylphosphonium SaltsBenzyltriphenylphosphonium salts (1) react with the aminal tert-butyl ester 2 to give [α-(dimethylaminomethylene)benzyl]triphenylphosphonium salts (3) or the corresponding ylenes, the benzylidenetriphenylphosphoranes (4). Hydrolysis of [α-(dimethylaminomethylene)-4-methoxybenzyl]triphenylphosphonium bromide tetrahydrate (3b · 4H2O) with aqueous potassium hydroxide results in elimination of benzene and formation of [α-(dimethylaminomethylene)-4-methoxybenzyl]diphenylphosphine oxide (8). Reaction of [α-(dimethylaminomethylene)benzyl]triphenylphosphonium bromide (3a) with sodium ethoxide affords ω-(dimethylamino)styrene (9) and triphenylphosphine oxide.
    Notes: Benzyltriphenylphosphonium-Salze (1) reagieren mit dem Aminal-tert-butylester 2 zu [α-(Dimethylaminomethylen)benzyl]triphenylphosphonium-Salzen (3) oder zu Ylenen, den Benzylidentriphenylphosphoranen (4). Die Hydrolyse von [α-(Dimethylaminomethylen)-4-methoxybenzyl]triphenylphosphonium-bromid-Tetrahydrat (3b · 4H2O) mit wäßriger Kalilauge führt unter Abspaltung von Benzol zu [α-(Dimethylaminomethylen)-4-methoxybenzyl]diphenylphosphinoxid (8). Mit Natriumäthylat entstehen aus [α-(Dimethylaminomethylen)benzyl]triphenylphosphoniumbromid (3a) ω-(Dimethylamino)styrol (9) und Triphenylphosphinoxid.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19731061132
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  • 7
    Electronic Resource
    Electronic Resource
    Synthesen in der heterocyclischen Reihe, XVIII. Synthese des Pyrimido[4,5-d]pyrimidins (1973)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 106 (1973), S. 3743-3752 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Syntheses in the Heterocyclic Series, XVIII. Synthesis of Pyrimido[4,5-d]pyrimidine4-Amino-5-pyrimidinecarbaldehyde dimethyl acetal (2a) as well as its 2-methyl (2b) and 2-phenyl derivative (2c) react with equimolar amounts of s-triazine in the heat to give the 4-(4-amino-5-pyrimidinylmethyleneamino)-5-pyrimidinecarbaldehyde dimethyl acetals 3a-c. With an excess of 5 moles of s-triazine 2a and c react after melting to yield the pyrimido[4,5-d]-pyrimidines 4a and c; under the same conditions 2b reacts to afford 4-(aminomethyleneamino)-2-methyl-5-pyrimidinecarbaldehyde (7). With an excess of 3 moles of s-triazine 2a and b react in the heat to give the 4-methoxy-3,4-dihydropyrimido[4,5-d]pyrimidines 8a and b.
    Notes: Aus molaren Mengen 4-Amino-5-pyrimidincarbaldehyd-dimethylacetal (2a) sowie dessen 2-Methyl- (2b) und 2-Phenyl-Derivat (2c) und s-Triazin entstehen in der Hitze die 4-(4-Amino-5-pyrimidinylmethylenamino)-5-pyrimidincarbaldehyd-dimethylacetale 3a-c. Mit einem 5-molaren Überschuß an s-Triazin erhält man nach einer Schmelzreaktion mit 2a und c die Pyrimido[4,5-d]pyrimidine 4a und c und mit 2b den 4-(Aminomethylenamino)-2-methyl-5-pyrimidincarbaldehyd (7). Mit einem 3-molaren s-Triazin-Überschuß entstehen in der Hitze mit 2a und b die 4-Methoxy-3,4-dihydropyrimido[4,5-d]pyrimidine 8a und b.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19731061133
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  • 8
    Electronic Resource
    Electronic Resource
    Orthoamid, XIV. Über die Umsetzung von p-Tolyl- und Anisaldehyd mit einem Aminal-tert.-butylester zu [1.2-Bis-dimethylamino-vinyl]-aryl-ketonen (1970)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 103 (1970), S. 2980-2983 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Orthoamides, XIV. On the Reaction of p-Tolyl- and Anisaldehyde with Formic Acid Bis(dimethylaminal) tert-Butyl Ester to [1,2-Bis(dimethylamino)vinyl]-aryl Ketones (4, 5). The reaction is supposed to proceed via bis(dimethylamino)methyl aryl ketone (A, which undergoes disproportionation in a kind of Cannizzaro reaction to yield dimethylaminomethyl aryl ketone 6, isolated as an intermediate.
    Notes: Aus tert-Tolyl(1) bzw. Anisaldehyd (2) entstehen mit Bis-dimethylamino-tert-. butyloxy-methan (3) [1.2-Bis-dimethylamino-vinyl]-aryl-aryl-ketone (4, 5). Ihre Bildung wird über ein intermediäres Bis-dimethylaminomethyl-aryl-keton (A gedeutet, das in einer Art Cannizzaro-Reaktion u.a. das als Zwischenprodukt isolierte Dimethylaminomethyl-aryl-keton 6 ergibt.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19701030935
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  • 9
    Electronic Resource
    Electronic Resource
    Orthoamide, IX über die Umsetzung CH-acider Verbindungen mit Amidacetalen, einem Aminal-tert.-butylester und Tris-dimethylamino-methan (1970)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 103 (1970), S. 210-221 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Orthoamides, IX: Reaction of CH-Acidic Compounds with Amide Acetals, an Aminal-tert-butylester and Tris(dimethylamino)methaneOrthoamides react with hydrogen cyanide and alkynes to give 2-dimethylamino-2-alkoxy-nitriles (2, 4, 6, 8, 10), 2,2-bis(dimethylamino)nitriles (12,12a), and 3,3-bis(dimethylamino)-alkynes (14-16). Methane derivatives heated with dimethylformamide diäthylacetal (1) react to form the alkylated methane derivatives (25, 26, 28, 29, 30, 34), whereas under mild conditions methane derivatives react with the aminal tert-butylester 11 to produce tetramethyl-formamidinium salts (31, 32, 33, 35).
    Notes: Orthoamide reagieren mit wasserfreier Blausäure und Alkinen zu 2-Dimethylamino-2-alkoxy-nitrilen (2, 4, 6, 8, 10), 2.2-Bis-dimethylamino-nitrilen (12, 12a) und 3.3-Bis-dimethylamino-alkinen-(l) (14-16). Aus Methan-Derivaten und Dimethylformamid-diäthylacetal (1) ent-stehen in der Wärme die alkylierten Methan-Derivate (25, 26, 28, 29, 30, 34) und mit dem Aminal-tert.-butylester 11 unter milden Reaktionsbedingungen die Tetramethylformamidini-um-Salze(31,32, 33,35).
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19701030129
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  • 10
    Electronic Resource
    Electronic Resource
    Hydroperoxide cyclischer β-Diketone1) (1970)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 739 (1970), S. 117-120 
    Details
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Hydroperoxides of Cyclic β-Diketones1)Autoxidation of cyclic β-diketones with a tert. α-C-atom gives hydroperoxides in benzenic solution.
    Notes: Bei der Autoxydation cyclischer β-Diketone mit einem tertiären C-Atom in α-Stellung entstehen in benzolischer Lösung Hydroperoxyde.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jlac.19707390115
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