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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 2865-2871 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Internal Mobility in the Ion Pairs during Aromatic Rearrangement of O-Sulfonyl-N-phenylhydroxylaminesIn the rearrangement of O-alkyl- or O-arylsulfonyl-N-benzoyl-N-phenylhydroxylamines 3 to aminophenols 4, the internal mobility in the ion pair intermediates depends both on the size of the alkyl groups and on the interaction with the protic solvent, as was shown by 18O labeled educts.
    Notes: Bei der Umlagerung von O-Alkyl- bzw. O-Arylsulfonyl-N-benzoyl-N-phenylhydroxylaminen 3 in Aminophenole 4 wird durch 18O-Indizierung gezeigt, daß die Beweglichkeit in den intermediär gebildeten Ionenpaaren durch große Alkylreste sowie durch Wechselwirkung mit einem protischen Lösungsmittel in typischer Weise verändert wird.
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  • 2
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Condensed Ring Systems, XV. About the Reaction of α-Chloro Sulfoxides with Potassium tert-Butoxide by the Example of the Synthesis of OxapropellenesThe synthesis of dithia- 1a - 3a and oxathiapropellenes 1b - 3b is described. From 1b - 3b the α-chloro sulfoxides 4 - 6 and α-chloro sulfones 4a - 6a are prepared, or which in most cases several stereoisomeric racemates are obtained. The constitution, configuration, and conformation of the α-chloro sulfoxide 4, the main product obtained from 1b, was elucidated by X-ray structure analysis. Only in that way it was possible to deduce the constitutions and configurations of the other stereoisomeric α-chloro sulfoxides 4 - 6 and α-chloro sulfones 4a - 6a, respectively, using 13C NMR spectroscopy. By the reaction of the α-chloro sulfones 4a - 6a with potassium tert-butoxide (Ramberg-Bäcklund reaction) the corresponding oxapropellenes 7 - 9 are obtained only in low yields (〈 10%). Contrary, the α-chloro sulfoxides 4 - 6, und analogous conditions give yields of 80 - 90% (from 4, 6) and 25% (from 5).
    Notes: Es wird die Synthese der Dithia- 1a - 3a und Oxathiapropellene 1b - 3b beschrieben. Aus 1b - 3b werden die α-Chlorsulfoxide 4 - 6 und α-Chlorsulfone 4a - 6a hergestellt, von denen meist mehrere stereoisomere Racemate erhalten werden. Konstitution, Konfiguration und Konformation des Hauptprodukts der aus 1b erhaltenen α-Chlorsulfoxide 4 wurden durch Röntgenstrukturanalyse ermittelt. Erst dadurch wurde es möglich, mit Hilfe der 13C-NMR-Spektroskopie die Konstitutionen und Konfigurationen der anderen stereoisomeren α-Chlorsulfoxide 4 - 6 und α-Chlorsulfone 4a - 6a aufzuklären. Bei der Reaktion der α-Chlorsulfone 4a - 6a mit Kalium-tert-butylat (Ramberg-Bäcklund-Reaktion) erhält man die entsprechenden Oxapropellene 7 - 9 nur in geringer Ausbeute (〈 10%), während die α-Chlorsulfoxide 4 - 6 unter analogen Bedingungen Ausbeuten von 80 - 90% (aus 4, 6) und 25% (aus 5) ergeben.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 9-14 
    ISSN: 0009-2940
    Keywords: Alkynyl groups ; Palladium, trimethylphosphane complexes ; Trimerization, oxidative ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Oxidative Trimerization of Alkynyl Groups at Trimethylphosphane Palladium ComplexesAlkynylpalladium halides trans-PdX (C ≡ CR)(PMe3)2 [1, 2, 4, X = Cl, R = SiMe3, (CH2)2CH3, (CH2)5CH3; 3, X = Br, R = (CH2)2CH3] were synthesized by routine methods, while further examples of the series trans-PdX (C ≡ CR)(PMe3)2 [5, 7, 8, 10, X = Br, R = SiMe3, CMe3, (CH2)2CH3, Ph; 7, 9, 11, X = I, R = SiMe3, SiPh3, OEt] and trans-PdX (C ≡ CR)(PPh3)2 (12-14, X=I, R=SiMe3, CMe3, CH2OH) were obtained by oxidative addition of 1-halogeno-1-alkynes to PdL4 (L=PMe3, PPh3). Just above the melting point or decomposition point 5-7 are transformed by oxidative trimerization of the alkynyl groups to give enediynyl complexes trans-PdX[C(C ≡ CR)=C(C ≡ CR)R](PMe3)2 (15, 16, R=SiMe3, X=Br, I; 17, X=Br, R=CMe3). According to an X-ray structure analysis 17 has E configuration.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 117 (1984), S. 2555-2579 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Lewis Acid Catalysed Addition Reactions of 1,3-Alkyl Substituted Allyl Chlorides with AlkenesThe zinc chloride-ether catalysed reactions of 2-unsubstituted allyl chlorides (5) with alkenes (6) yield linear addition products (7) which may undergo two types of sequential reactions: Electrophilic additions to alkenes (allyl chloride induced polymerisation of alkenes) and allylation of the double bond in 7 by allyl chloride (alkene induced polymerisation of allyl chlorides). In this work we investigated systems where these sequential reactions can be reduced to a degree that electrophilic allylations of alkenes represent a synthetically useful method for CC-bond formation. - The addition reactions are not stereospecific but highly regioselective: alkenes are attacked in Markownikow sense and unsymmetrical allylic systems react at the less substituted allyl terminus. In two cases, [2 + 2]-cycloaddition reactions of allyl cations with alkenes are observed.
    Notes: Die Zinkchlorid-Ether-katalysierten Umsetzungen 2-unsubstituierter Allylchloride (5) mit Alkenen (6) liefern lineare Additionsprodukte (7), die zwei Arten von Folgereaktionen eingehen können: Elektrophile Additionen an Alkene (Allychlorid-induzierte Polymerisation der Alkene) und Allylierung der Doppelbindung von 7 durch Allylchlorid (Alken-induzierte Polymerisation der Allylchloride). Es wird untersucht, bei welchen Systemen diese Folgereaktionen soweit zurückgedrängt werden können, daß elektrophile Allylierungen von Alkenen eine präparativ brauchbare Methode zur CC-Verknüpfung darstellen. - Die Additionsreaktionen sind nicht stereospezifisch, zeigen jedoch hohe Regioselektivität: Alkene werden in Markownikow-Richtung angegriffen, unsymmetrische Allylsysteme am weniger substituierten Ende. In zwei Fällen werden [2 + 2]-Cycloadditionen von Allylkationen beobachtet.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 116 (1983), S. 3624-3630 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis of 1,2,3,3,6,6-Hexamethyl-l-cyclohexene - A Cascade of C12H+ Carbenium Ion Rearrangements6-Chloro-2,6,7,7-tetramethyl-2-octene (4), prepared via prenyl chloride addition to 2,3,3-trimethyl-1-butene, at room temperature undergoes a zinc chloride/hydrogen chloride-catalysed cyclocondensation to yield 1,2,3,3,6,6-hexamethyl-1-cyclohexene (1). The reaction mechanism is elucidated by isolation of intermediate five-membered carbocycles and by force field calculations.
    Notes: 6-Chlor-2,6,7,7-tetramethyl-2-octen (4), das Prenylchlorid-Additionsprodukt an 2,3,3-Trimethyl-1-buten, geht bei Raumtemperatur in Gegenwart von Zinkchlorid und Chlorwasserstoff eine Cyclokondensation unter Bildung von 1,2,3,3,6,6-Hexamethyl-1-cyclohexen (1) ein. Der Reaktionsmechanismus wird durch die Isolierung intermediär auftretender fünfgliedriger Ringe und durch Kraftfeldrechnungen aufgeklärt.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 1209-1223 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: A Stereoselective Synthesis for Aminobicyclo[n.1.0]alkanes of Various Ring SizeEnaminosulfonium chlorides 8 are valuable intermediate products for synthesizing aminobicyclo-[n.1.0]alkanes of various ring size. Transformation of 8 to the fluorosulfate 9 and its reaction with succinimide (10) gives isolable cis-linked succinimido-bicycloalkanes 12 with 99 percent purity even with medium-large ring systems. The endo-morpholino configuration is assigned by temperature dependent 1H NMR spectroscopy; the structure 12f was proved by X-ray structure analysis. Reaction of 8e-g to the chloroenamines 13e-g followed by an interaction with 10 leads to the trans-bicyclic compounds 14e-g with a selectivity of 95-98%. With these syntheses the bicyclic derivatives 12 or 14 are obtained without isolation of intermediate products 8,9, or 13 from enamines 5, dimethyl sulfide, and N-chlorosuccinimide.
    Notes: Enaminosulfonium-chloride 8 sind wertvolle Zwischenprodukte zur Herstellung von Aminobicyclo[n.1.0]alkanen verschiedener Ringgröße. Nach der Überführung von 8 in das Fluorosulfat 9 werden mit Succinimid (10) die cis-verknüpften Succinimidobicyclen 12 erhalten, die auch im Bereich mittlere-größere Ringe mit über 99proz. Reinheit isolierbar sind. Die Ermittlung der endo-Morpholino-Konfiguration erfolgt durch temperaturabhängige 1H-NMR-Spektroskopie; für 12f wurde eine Röntgenstrukturanalyse durchgeführt. Reaktion von 8e-g zu den Chlorenaminen 13e-g und anschließende Umsetzung mit 10 führt zu den trans-Bicyclen 14e-g in einer Selektivität von 95-98%. Bei diesen Synthesen werden die Verbindungen 12 oder 14 ohne Isolierung von Zwischenprodukten 8,9 oder 13 aus Enaminen 5, Dimethylsulfid und N-Chlorsuccinimid erhalten.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 1589-1595 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Electron-Excess Complexes of Cobalt and Nickel with Cyclobutadiene Ligands: Syntheses, Cyclovoltammetry, and Reactivity[1]A cyclovoltammetric investigation of tetraphenylcyclobutadiene complexes [ML(C4Ph4)]+ [1: ML = NiCp; 2a: ML = Co(C6H6); 2b: ML = Co(mesitylene)] reveals a reversible reduction to paramagnetic complexes 1 and 2a,b with a 19-electron count, and a subsequent irreversible reduction to anions 1- and 2a,b- with a 20-electron shell. Preparative reduction by one equivalent of CpFe(HMB) (HMB = C6Me6) produces the novel 19-electron complexes 1 and 2b. Complex 1 can also be obtained by treatment of 1 · Br with one equivalent of CoCp2 at room temperature while reduction at -20°C with two equivalents of CoCp2 affords a novel C-C-linked adduct CpNi[μ,η3:η4-(C4Ph4-C5H5)]CoCp (5). Above -10°C a slow equilibrium between 5 and its components 1 and CoCp2 is observed with ΔH = 15 kJ/mol for the dissociation process. With an excess of the stronger reductant sodium amalgam the cations 1+ and 2a+ are reduced to give cyclobutenyl complexes ML(η3-1,2,3,endo-4-C4HPh4) [6: ML = NiCp; 7: ML = Co(C6H6)]. 1 reacts with p-nitrobenzyl bromide to give 1 Br and a p-nitrobenzyl addition product CpNi[η3-exo-4-(p-O2NC6H4CH2)-1,2,3,endo-4-C4Ph4] (11) while 2b reacts with MeI to give 2b · I and two isomeric methyl addition products (η5-1,3,5,exo-6-C6H3Me4)Co(C4Ph4)] (12) and (mes)Co(η3-exo-4-Me-1,2,3,endo-4-C4Ph4) (13). Sodium-amalgam reduction of the tetramethylcyclobutadiene cations [(arene)Co(C4Me4)]+ (4a: arene = C6H6; 4b: arene = mesitylene) affords diamagnetic dinuclear compounds of type 8-10 with C-C linkages between C4Me4/C4Me4, arene/C4Me4, and arene/arene rings, respectively.
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  • 8
    ISSN: 0009-2940
    Keywords: Allylamine nickel complexes ; Allylamine cobalt complexes ; 2D NMR, TOCSY ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 16-Electron complexes of zerovalent nickel with diallylamines, Ni[(C3H5)2NR]L [1, 2: L = P(CH3)3, R = CH3, C6H5; 3: L = P(C6H5)3, R = CH3] and [NiP(CH3)3]2CH2[N(C3H5)2]2 (4), were synthesized by reduction of NiCl2L2 with magnesium in tetrahydrofuran. NiCl(η3-C3H5)[P(CH3)3]2 (5), a low-yield byproduct, was also obtained in high yield from NiL4 and C3H5Cl. With triallylamine as starting material complexes Ni[(C3H5)3N]L [6: L = P(CH3)3; 7: L = P(C6H5)3] were generated exhibiting η6- and η4-olefin coordination, respectively. 17-electron cobalt(O) compounds Co[(C3H5)2NR](PMe3)2 (8, 9: R = CH3, C6H5) were obtained by reaction of Co(cyclo-C5H8)(PMe3)3 with the corresponding diallylamine, while CoR(PMe3)4 (R = CH3, C6H5) reacted with N,N-diallylaniline to give diagmagnetic Co[(η3-C3H4)(η2-C3H5)NC6H5](PMe3)2, (10). The coordination mode of allylic functions was deduced from IR, ESR and especially 1H- and 13C-NMR spectra including 2D-NMR experiments.
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  • 9
    ISSN: 0009-2940
    Keywords: Alkynylnickel halides ; Nickel complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Oxidative Linear Trimerization of Alkynyl Groups in (Trimethylphosphane)nickel Complexes: Structures and the Role of Ligand-Rich Precursors NiX(C≡CR)(PMe3)n (n = 2-4)Oxidative additions of 1-halogenoalkynes XC≡CR; to Ni(PMe3)4 afford high yields of pentacoordinate ionic alkynylnickel compounds [Ni(C≡CR)(PMe3)4]+X- [R = SiMe3, X = I (1); R = CMe3, X = I (2), Br (3); R = SiEt3, X = I (6), Br (7); R = SiiPr3, X = I (10), Br (11), R = Ph, X = I (21), Br (22)] or complex molecules Ni(C≡CR)X(PMe3)3 [R = SiPh3, X = I (14), Br (15); R = Ph, X = I (19), Br (20)]. Dissociation of trimethylphosphane gives square planar trans-Ni(C≡CR)X-(PMe3)2 [R = CMe3, X = Br (4), Cl (5); R = SiEt3, X = Br (8), Cl (9); R = SiiPr3, X = Br (12), Cl (13); R = SiPh3, X = I (16), Br (17), Cl (18); R = Ph, X = I (23), Br (24), Cl (25)] but with R = SiR'3, X = I the title reaction dominates with formation of trans-Ni[C(C≡CR)=CR(C≡CR)]I(PMe3)2 [R = CMe3 (26), SiEt3 (29), SiiPr3 (32)]. Thermal activation is necessary in order to obtain trans-Ni[C≡CR)=CR(C≡CR)]X(PMe3)2 [R = CMe3, X = Br (27), Cl (28); R = SiEt3, X = Br (30), Cl (31); R = SiiPr3, X = Br (33), Cl (34)], while only thermal decomposition is observed with trans-Ni(C≡CR)X(PMe3)2 (R = Ph, SiPh3). Examples for both types of reactivity including structural data are given: trans-Ni(C≡CRSiMe3)Br(PMe3)2 and 25 crystallize in the space group P1. Pentacoordinate 19 (space group P21) adopts a trigonal pipyramid of ligand donor atoms with equatorial phenylethynyl and iodo ligands.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 2795-2806 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Enaminosulfonium Salts, Starting Materials for a Stereoselective Synthesis of Aminobicyclo-[n.1.0]alkanesEnaminosulfonium salts 6 react with sodium formate to give aminobicyclo[n.1.0]alkanes 1. Products 1 may also be obtained from the succinimido derivatives 4 formed via 6. They are converted into 1 either directly with triethylammonium formate or via the methoxy compound 7 and lithium aluminium hydride. In the area of medium to large ring systems specifically cis- or trans derivatives 1 and 3, resp., are prepared. The endo-amino configuration of 1 is established by the 3JHH coupling constants. Surprisingly, the assignment of configuration via dynamic 1H NMR spectroscopy which works very well with substituted aminobicyclo[n.1.0]alkanes is not applicable to 1 and 2 containing a six-membered heterocycle.
    Notes: Enaminosulfonium-Salze 6 reagieren mit Natriumformiat zu Aminobicyclo[n.1.0]alkanen 1. Zur Herstellung von 1 können auch die aus 6 zugänglichen Succinimidobicyclen 4 eingesetzt werden. Sie werden entweder direkt durch Triethylammoniumformiat oder über die Methoxyderivate 7 durch Lithiumalanat in 1 übergeführt. Im Bereich mittlere-größere Ringe lassen sich so gezielt cis-oder trans-Bicyclen 1 bzw. 3 erhalten. Die endo-Aminokonfiguration 1 folgt aus den 3JHH-Kopplungskonstanten. überraschenderweise ist die bei substituierten Aminobicyclo[n.1.0]alkanen gefundene Konfigurationszuordnungsmethode über die dynamische 1H-NMR-Spektroskopie für Verbindungen 1 und 2 mit einem Sechsring-Heterocyclus nicht anwendbar.
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