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  • 1
    Call number: PIK B 404-06-0304 ; M 06.0572
    Type of Medium: Monograph available for loan
    Pages: 116 S. + 1 CD-ROM
    Edition: 1. Auflage
    ISBN: 3448079014
    Location: A 18 - must be ordered
    Location: Upper compact magazine
    Branch Library: PIK Library
    Branch Library: GFZ Library
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  • 2
    Call number: 1.7/S 05.0606 + NBM 05.0606
    Type of Medium: Monograph available for loan
    Pages: Losebl.-Ausg. + CD-ROM
    ISBN: 3448066575 , 3-448-07291-5
    Location: Reading room
    Branch Library: GFZ Library
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 116 (1983), S. 1756-1776 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis of 3,4-and 3,5-Disubstituted λ3-and λ5-Phosphorins from 5-Aryl-1-tert-butyl-1,6-dihydro-4-methyl-3(2H)-phosphorinone 1-OxidesStarting from di(1-butynyl)-tert-butylphosphane (4) by reaction with aryl(bromomethyl)ketones the 4-(1-butynyl)-4-tert-2-ethyl-6-R-4H-1,4-oxaphosphorin-4-ium bromides 5 are formed. By alkaline degradation 5 give the 4-tert-butyl-2-ethyl-6-R-H-1,4-oxaphosphorin 4-oxides 6. Treatment of 6 with refluxing ethanolic hydrochloric acid induces ether cleavage followed by aldol condensation to give the 5-aryl-1-tert-butyl-1,6-dihydro-4-methyl-3(2H)-phosphorinone 1-oxides (7). Reduction of 7 with silicochloroform leads to the 3-aryl-1-tert-butyl-1-chloro-4-methyl-λ5-phosphorins 8, which are thermolyzed at 250 - 270°C to give the 3-aryl-1-tert-butyl-4-methyl-λ3-phosphorins 9 in good yields. During the reaction of 7 with silicochloroform 1,2-migration of the methyl group occurs to some extent - depending on the nature of the aryl group - and the 3-aryl-1-tert-butyl-1-chloro-5-methyl-λ5-phosphorins 12 are formed, which are thermolyzed to give the corresponding 3-aryl-5-methyl-λ3-phosphorins 10. - The 1H NMR, 13C NMR, 31P NMR, IR, UV, and mass spectra are discussed.
    Notes: Ausgehend von Di(1-butinyl)-1-tert-butylphosphan (4) werden durch Umsetzung mit Aryl(brommethyl)ketonen die 4-(1-Butinyl)-4-tert-butyl-2-ethyl-6-R-4H-1,4-oxaphosphorin-4-ium-bromide 5 erhalten. Der Alkaliabbau von 5 liefert die 4-tert-Butyl-2-ethyl-6-R-4H-1,4-oxaphosphorin-4-oxide 6, die in siedender ethanolischer Salzsäure unter Etherspaltung und anschließender Aldolkondensation in die 5-Aryl-1-tert-butyl-1,6-dihydro-4-methyl-3(2H)-phosphorinon-1-oxide (7) übergehen. Bei der Reduktion von 7 mit Silicochloroform werden die 3-Aryl-1-tert-butyl-1-chlor-4-methyl-λ5-phosphorine 8 gebildet, die sich bei 250-270°C in guten Ausbeuten zu den 3-Aryl-4-methyl-λ3-phosphorinen 9 thermolysieren lassen. Im Verlaufe der Umsetzung von 7 mit Silicochloroform kommt es - in Abhängigkeit vom Arylrest - zum Teil zu einer 1,2-Methylverschiebung zu den 3-Aryl-1-tert-butyl-1-chlor-5-methyl-λ5-phosphorinen 12, die bei der Thermolyse die 3-Aryl-5-methyl-λ3-phosphorine 10 ergeben. - Die 1H-NMR-, 13C-NMR-, 31P-NMR-, IR-, UV- und Massenspektren werden diskutiert.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 116 (1983), S. 445-472 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 3-Aryl-λ3-phosphorins, 3-Aryl-λ5-phosphorins, 3-Aryl-λ4-phosphorinium SaltsBy reaction of tert-butyldi(1-propynyl)phosphane (3) with (bromomethyl)ketones 4 the 4-tert-butyl-2-methyl-4-(1-propynyl)-6-R-4H-oxaphosphorin-4-ium bromides 6 are obtained, which are degraded by hydrolysis to the 4-tert-butyl-2-methyl-6-R-1,4-oxaphosphorin 4-oxides 7. These oxides undergo an acid-catalyzed aldol-condensation to form the 1-tert-butyl-1,6-dihydro-5-R-3(2H)-phosphorinone 1-oxides 1. Compounds 1 (R = Ar) react with silicochloroform to give the 3-aryl-1-tert-butyl-1-chloro-λ5-phosphorins 11, the structure of which is proved by transformation into the 3-aryl-1-tert-butyl-1-fluoro(1-methoxy)-λ5-phosphorins 12 and 13, respectively. The spectroscopic properties indicate that in polar solvents 1-tert-butyl-1-chloro-3-phenyl-λ5-phosphorin (11a) forms an equilibrium with 1-tert-butyl-3-phenyl-λ4-phosphorinium chloride (18a) with 4-bonding phosphorus, coordination number 3. - The mechanism of the formation of 3-aryl-1-tert-butyl-1-chloro-λ5-phosphorins 11 is discussed. It is proved by the reaction of 1-tert-butyl-1,2-dihydro-3-phenylphosphorin 1-oxide (14a) with silicochloroform by which 11a is formed. - Thermolysis of the 3-aryl-1-tert-butyl-1-chloro-λ5-phosphorins 11 at 250-300°C affords the 3-aryl-λ3-phosphorins 2, which form the 3-aryl-1,1-dimethoxy-λ5-phosphorins 21 by oxidative alkoxylation with Hg(OAc)2/methanol. - The IR, UV, 1H NMR, 13C NMR and, mass spectra of the various classes of compounds are discussed, the high-resolution 1H NMR spectra of some λ5-phosphorins and of the λ3-phosphorins are calculated according to LAOCOON-LAME and DAVINS, respectively.
    Notes: Die durch Reaktion von tert-Butyldi(1-propinyl)phosphan (3) mit (Brommethyl)ketonen 4 erhältlichen 4-tert-Butyl-2-methyl-4-(1-propinyl)-6-R-4H-1,4-oxaphosphorin-4-ium-bromide 6 werden zu den 4-tert-Butyl-2-methyl-6-R-1,4-oxaphosphorin-4-oxiden 7 hydrolysiert, die durch säurekatalysierte Aldolkondensation in die 1-tert-Butyl-1,6-dihydro-5-R-3(2H)-phosphorinon-1-oxide 1 übergeführt werden. Bei deren Umsetzung (R = Ar) mit Silicochloroform entstehen die 3-Aryl-1-tert-butyl-1-chlor-λ5-phosphorine 11, deren Konstitution durch Umwandlung in die 3-Aryl-1-tert-butyl-1-fluor(1-methoxy)-λ5-phosphorine 12 bzw. 13 bewiesen wird. Die spektroskopischen Eigenschaften lassen die Annahme zu, daß das 1-tert-Butyl-3-phenyl-λ5-phosphorin (11a) in polaren Solventien im Gleichgewicht mit dem 1-tert-Butyl-3-phenyl-λ4-phosphorinium-chlorid (18a) mit 4-bindigem Phosphor, K. Z.3, vorliegt. - Der Mechanismus der Bildung der 3-Aryl-1-tert-butyl-1-chlor-λ5-phosphorine 11 wird diskutiert. Er wird mit der Umwandlung von 1-tert-Butyl-1,2-dihydro-3-phenylphosphorin-1-oxid (14a) in 11a mit Silicochloroform bewiesen. - Die Thermolyse der 3-Aryl-1-tert-butyl-1-chlor-λ5-phosphorine 11 bei 250-300°C liefert die 3-Aryl-λ3-phosphorine 2, die sich mit Hg(OAc)2/Methanol zu den 3-Aryl-1,1-dimethoxy-λ5-phosphorinen 21 oxidieren lassen. - Die IR-, UV-, 1H-NMR-, 13C-NMR- und Massenspektren der einzelnen Verbindungsklassen werden diskutiert, die hochaufgelösten 1H-NMR-Spektren einiger λ5-Phosphorine und der λ3-Phosphorine werden nach LAOCOON-LAME bzw. DAVINS gerechnet.
    Additional Material: 10 Tab.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 117 (1984), S. 763-782 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis of 3,5-Disubstituted and 3,4,5-Trisubstituted λ3-Phosphorins from 1-tert-Butyl-1,6-dihydro-3(2H)-phosphorinones5-Aryl-1-tert-butyl-1,6-dihydro-3(2H)-phosphorinones 13 - easily available by reduction of the phosphane oxides 1 with phenylsilane - react with 1 mol of RMgX (RLi) exclusively by formation of the enolates, however with 6 mol of RMgX (RLi), after reaction times of several days, immediately the 3-aryl-1-tert-butyl-1,2-dihydro-5-R-phosphorins 10 are formed, which can be thermolyzed to give the 3-aryl-5-R-λ3-phosphorins 11 (R = aryl, alkyl, heteroaryl). - 5-Aryl-1-tert-butyl-1,6-dihydro-4-methyl-3(2H)-phosphorinones 19 react with 5 - 6 mol of RMgX (RLi) similar by formation of the 3-aryl-1-tert-butyl-1,2-dihydro-4-methyl-5-R-phosphorins 20, whose thermolysis yields the 3-aryl-4-methyl-5-R-λ3-phosphorins 21. The 1H, 13C, 31P NMR and UV spectra of the synthesized λ3-phosphorins are discussed. - 1,1-Dimethoxy-3,5-diphenyl-λ5-phosphorin (22a), available from 3,5-diphenyl-λ3-phosphorin (11e), undergoes coupling reaction with diazonium salts to give the 2,4,6-tris(arylazo)-1,1-dimethoxy-3,5-diphenyl-λ5-phosphorins 23.
    Notes: 5-Aryl-1-tert-butyl-1,6-dihydro-3(2H)-phosphorinone 13 - durch Reduktion der Phosphanoxide 1 mit Phenylsilan glatt zugänglich - reagieren mit 1 mol RMgX (RLi) ausschließlich unter Bildung der Enolate, mit 6 mol RMgX (RLi) hingegen werden nach mehrtägigen Reaktionszeiten direkt die 3-Aryl-3-tert-butyl-1,2-dihydro-5-R-phosphorine 10 erhalten, die bei der Thermolyse zu den 3-Aryl-5-R-λ3-phosphorinen 11 (R = Aryl, Alkyl, Heteroaryl) zerfallen. - 5-Aryl-1-tert-butyl-1,6-dihydro-4-methyl-3(2H)-phosphorinone 19 reagieren mit 5 - 6 mol RMgX (RLi) entsprechend zu den 3-Aryl-1-tert-butyl-1,2-dihydro-4-methyl-5-R-phosphorinen 20, deren Thermolyse die 3-Aryl-4-methyl-5-R-λ3-phosphorine 21 liefert. - Die 1H-, 13H-, 13C-, 31P-NMR- und UV-Spektren der dargestellten λ3-Phosphorine werden diskutiert. - Das aus 3,5-Diphenyl-λ3-phosphorin (11e) zugängliche 1,1-Dimethoxy-3,5-diphenyl-λ5-phosphorin (22a) kuppelt mit Diazoniumsalzen zu den 2,4,6-Tris(arylazo)-1,1-dimethoxy-3,5-diphenyl-λ5-phosphorinen 23.
    Additional Material: 4 Ill.
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