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  • 1
    ISSN: 1434-1948
    Keywords: Arenetricarbonyl chromium complexes ; Palladium ; Cross coupling reaction ; Thiophenes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The cross coupling reaction of (p-chloroanisole)tricarbonylchromium complex (1) with thiophene derivatives under palladium-catalyzed conditions leads to the selective formation of tricarbonyl-η6-[(2-thiophenyl)arene]- or -η6-[(2-thiophenyl)carbonylarene]chromium complexes (2 or 3) depending on reaction conditions. The conformation of complexes 2 and 3 in the solid state as well as in solution are reported.
    Additional Material: 4 Ill.
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  • 2
    ISSN: 1434-1948
    Keywords: Radicals ; Carbenium ions ; Clusters ; Cobalt ; Molybdenum ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Complexed α-CF3 propargyl alcohols of the general formula [(M2L6){μ-η2,η2-RC≡CCH(CF3)(OH)}] were prepared with M2L6 = Co2(CO)6, R = CH3(CH2)4- (1), R = C6H5- (2); M2L6 = Co2(CO)5P(C6H5)3, R = CH3(CH2)4- (3a,b), R = C6H5- (4a,b); M2L6 = Co2(CO)4dppm, R = C6H5- (5); M2L6 = Co(CO)3MoCp(CO)2, R = CH3(CH2)4- (6a,b), R = C6H5- (7a,b). An X-ray molecular structure of the propargyl-alcohol complex [{Co2(CO)4dppm}{μ-η2,η2-C6H5C≡CCH(CF3)(OH)}] (5) was also determined. The related carbenium ions [(M2L6){μ-η2,η3-RC≡CCH(CF3)}][BF4] (8-12) were obtained from the parent propargyl alcohol complexes by direct protonation with HBF4· Et2O in diethyl ether. These carbenium ions were reduced further by Zn in CH2Cl2 to give the alkyne adducts [(M2L6){μ-η2,η2-RC≡CCH2(CF3)}] (13-17), as confirmed by the X-ray molecular structure of [(Co2(CO)4dppm){μ-η2,η2-C6H5C≡CCH2(CF3)}] (17). Treatment of the carbenium ion complex [{Co(CO)3MoCp(CO)2}{μ-η2,η3-CH3(CH2)4C≡CCH(CF3)}][BF4] (8) with NaSMe unexpectedly afforded the reduced alkyne adduct [{Co(CO)3MoCp(CO)2}{μ-η2,η2-CH3(CH2)4C≡CCH2(CF3)}] (13), along with the alkyne-thioether diastereomers {Co(CO)3MoCp(CO)2}{μ-η2,η2-CH3(CH2)4C≡CCH(CF3)[(SMe)}] (18a,b). Presumably, all the reduction reactions proceed primarily by the formation of the transient radical species, which are subsequently transformed into the reduced alkyne complexes by hydrogen abstraction from the solvent medium. Interestingly, in the case of the complexed alcohols [{Co2(CO)5P(C6H5)3}{μ-η2,η2-RC≡CCH(CF3)(OH)}] (3a,b) and (4a,b), the reduction process occurs in acidic medium in THF/CH2Cl2. An extensive study of the electronic and steric factors that influence the stability and reactivity of the carbenium ions were performed, which allowed us to explain the behavior of the related radical species in solution during the reduction process.
    Additional Material: 4 Ill.
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  • 3
    ISSN: 1434-1948
    Keywords: Arene complexes ; Chromium ; Cyclohexadienyl complexes ; Dinuclear complexes ; Manganese ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of secondary α-cyano or α-sulfonyl carbanions with cationic (η6-arene)tricarbonylmanganese complexes affords neutral mono- and dinuclear tricarbonyl(η5-cyclohexadienyl)manganese complexes. The X-ray analyses of three (η5-cyclohexadienyl)Mn complexes (two mononuclear and one dinuclear) obtained by addition of α-cyano carbanion to cationic (η6-arene)manganese complexes are reported. The addition of benzylic carbanions of (η6-arene)tricarbonylchromium complexes to cationic (η6-arene)manganese complexes gives rise to the formation of the corresponding heterodinuclear [(η5-cyclohexadienyl)manganese-(η6-arene)chromium] complexes.
    Additional Material: 3 Ill.
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  • 4
    ISSN: 1434-193X
    Keywords: Chromium ; Aminocarbene complexes ; Alkynes ; C-H activation ; Quinolizines ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: N-alkynyl aminocarbene complexes 15d and e derived from piperidin-2-one, 15f and g and from azepan-2-one yield, upon thermolysis, functionalized quinolizines 16-18d,e and homoquinolizines 16-18f,gas the result of a triple-bond insertion, a carbon-hydrogen bond activation, followed by a CO insertion. No reaction was observed in the case of complexes derived from pyrrolidin-2-one.
    Additional Material: 2 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 2000 (2000), S. 83-90 
    ISSN: 1434-193X
    Keywords: Amino acids ; Diastereoselective alkylation ; Oppolzer's sultam ; Sultam-imine enolate ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---As part of an ongoing project concerning the synthesis of nonnatural amino acids, we have now developed a general strategy for the preparation of β2-amino acids (or 2-aminocarboxylic acid derivatives). Our procedure involves the synthesis of the sultam β-alaninate precursor 5 whose alkylation led with high yields and excellent diastereoselectivity to the precursor of β2-homophenylalanine, β2-homoalanine, and β2-homoleucine. Subsequent deprotection and Boc-protection yielded the expected β2-amino acids. X-ray analysis of the alkylation product established that (-)-sultam yielded (R)-β2-amino acids, conversely (+)-sultam yielded the enantiomer. The topicity of this alkylation is in agreement with the alkylation of Oppolzer's precursor for the synthesis of α-amino acids and opposite to that observed for gem-dialkylation.
    Additional Material: 1 Ill.
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  • 6
    ISSN: 1434-193X
    Keywords: Chromium ; Carbene complexes ; N-ylide complexes ; Thio and selenophenols ; Acetic acid ; Acetic acid ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Aminocarbene complexes of chromium 1b-d react successively with diphenylacetylene, XH (X = PhS, PhSe, OAc) and finally with pyridine to give a series of functionalized pyrrolinones 7 via N-ylide complexes 2. The X-ray structure of 7b originating from a ring-opening reaction could be established. When this sequence was applied to the aminocarbene complex 8 bearing a tethered triple bond, synthesis of functionalized 2-oxohexahydroindole 11 was achieved. In the case of acetic acid, products resulting from a formal protonation/hydride addition reaction together with a carbon-nitrogen bond rupture were also observed besides protonation/dealkylation products.
    Additional Material: 1 Ill.
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