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  • 1
    ISSN: 0009-2940
    Keywords: Carbene complexes of chromium and tungsten ; 1-Metalla-1,3,5-trienes ; 1-Metalla-1,3-dien-5-ynes ; Insertion of alkynes into M=C and C=C bonds ; [2 + 2] Cycloaddition reactions of carbene complexes and alkynes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organic Syntheses via Transition Metal Complexes, 51. - 1-Metalla-1,3,5-trienes and 1-Metalla-1,3-dien-5-ynes of Chromium and Tungsten by Insertion of Alkynes into M=C and C=C Bonds of 1-Metalla-1,3-dienes and 1-Metalla-1-en-3-ynes, respectively1-Metalla-1,3,5-trienes LnM=C(NEt2)-C(Me)—C(OEt)-CH=CHPh (3,4) and LnM=C(OEt)- CH=C(NEt2) - C(Me)=CHPh [5, LnM=Cr(CO)5 (a), W(CO)5 (b)] are obtained for the first time from the corresponding 1-metalla-1,3-dienes LnM=C(OEt) - CH=CHPh (1a, b) under very mild conditions by the insertion of the electron-rich alkyne Et2N-C ≡ C - Me (2) into the M=C and the C=C bonds, respectively, of 1. The chelate complex (6b) and the cyclobutenyl carbene complex 7b are isolated as minor side products. 1-Metalla-1,3-dien-5-ynes LnM=C(NEt2) - C(Me)=C(OEt) - C ≡ CPh [9, 10, LnM=Cr(CO)5 (a), W(CO)5 (b)] are formed with high regio- and stereoselectivity on insertion of 2 into the M=C bonds of 1-metalla-1-en-3-ynes 8. X-ray data are given for the tungsten complex 3b.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0009-2940
    Keywords: Carbene complexes of chromium and tungsten ; Alkenylcarbene complexes, protonation of ; β-(Acylamino)alkenyl complexes of chromium ; Activated aminocarbene complexes ; 1-Metalla-1,3-dienes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organic Syntheses via Transition Metal Complexes, 46.  -  Alkenylcarbene Chromium and Tungsten Complexes; Proton Addition and Activation by Electron-Withdrawing SubstituentsAlkenylcarbene complexes LnM=C(OEt)-CH=C(R)NMe2[1, LnM = Cr(CO)5, W(CO)5; R = H, CH3, C6H5] add HBF4 in ether to give novel cationic carbene complexes [Ln M=C(OEt)-CH2-C(R)=NMe2]BF4 (3) by protonation at C-2 of the =C-C=C ligand. The addition of HBF4 to 7 leads to the formation of the cyclic carbene complexes 8. Structures of 3 and 8 are assigned spectroscopically. X-ray data are reported for 8a. Protonation of 1 and 7 results in a strong deshielding of the carbene carbon atoms, which parallels an increase of reactivity at the M=C bonds. An activation of the M=C bond has also been achieved by electron-withdrawing substituents like N-acyl groups. We report on the first synthesis of [β-(acylamino)-alkenyl]carbene complexes 13, which are more reactive than β-(aminoalkenyl)carbene complexes 7.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0009-2940
    Keywords: Carbene complexes of chromium and tungsten ; 1-Metalla-1,3-dienes ; Insertion of alkynes and isocyanides into M = C bonds ; 2H-Pyrrole complexes of chromium and tungsten ; [1+2+2] Cycloaddition reactions of carbene complexes, alkynes and isocyanides ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organic Syntheses via Transition Metal Complexes, 501). - 2H-Pyrrole Complexes by a Stepwise Insertion of Alkynes and Isocyanides into M=C Bonds of Carbene Chromium or Tungsten Complexes2H-Pyrrole complexes 6a, b are obtained in two step by [1+2+2] cycloaddition reactions of the carbene complex (CO)5W=C(OEt)C6H5 (1d), the alkyne EtO-C≡CH (2) and isocyanides R1-NC 4a, b [R1 = CH3, c-C6H11). Ln=C(OEt)R 1 [LnM = Cr(CO)5, W(CO)5; R = C6H5, CH3] reacts with 2 to give 1-metalla-1,3-dienes 3a-d. (E)/(Z)-3d and 4 yield 6a, b via 1-aza-1,2,4-pentatriene complexes 5, which are open-chain precursors of 6. 2H-Pyrrole complexes 11 and 14 are synthesized in overall [2+1+2] cycloadditions withe reversed connectivity, or formation of 1-chroma-1,3-dienes 10 and 13 by condensation of the methylcarbene complex 1a with acid amides, and cyclisation again with isocyanides 4.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1867-1872 
    ISSN: 0009-2940
    Keywords: Aminobenzannulation with isocyanides ; 1,4-Diaminonaphthalines ; Alkynylcarbene complexes ; β-Aminovinylcarbene complexes ; Dienylketenimine complexes ; 4-Amino-1-chroma-1,3-dienes ; Chromium complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organic Syntheses via Transition Metal Complexes, 64[1]. - 1,4-Diaminonaphthalines via Ketenimine Complexes from (β-Aminovinylcarbene)chromium Complexes and IsocyanidesThe thermal reaction of (dienylcarbene)chromium complexes (= 1-chroma-1,3,5-trienes) with isocyanides provides a mild and regiospecific access to aromatic amines. Thus, 1,4-diamino-2-ethoxynaphthalines 6a-d [1-NHc-C6H11; 4-NRR1 = NMe2 (a) (S)-2-hydroxymethylpyrrolidinyl (b) (1R,2S)-2-methylamino-1-phenyl-1-propanol (c), NtBuMe (d)] are obtained by the cyclization of (E)-(β-aminostyrylcarbene)chromium complexes (CO)5Cr=C(OEt)CH=C(NRR1)C6H5 [(E)-3a-d] with cyclohexyl isocyanide (4) at 90°C in 72-85%. The aminocarbene complexes (E)-3a-d are accessible with high stereoselectivity [〉95% (E) configuration] and chemical yields of 91-96% by the addition of secondary amines HNRR1 2a-d to the (1-alkoxy-3-phenylpropynylidene)chromium complex (CO)5Cr=C(OEt)C≡CC6H5 (1). 3 and 4 give initially mono- and bis(isocyanide) complexes, e.g. (E)-8a and (E)-9a, and subsequently dienylketenimine complexes by the insertion of 4 into the M=C bond of 3. Dienylketenimine complexes are key intermediates in the formation of 6.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 2475-2482 
    ISSN: 0009-2940
    Keywords: Vinylcarbene complexes ; Chromium complexes ; Tungsten complexes ; Phosphorus ylide complexes ; Alkynylcarbene complexes ; Allene complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Alkynylcarbene complexes (CO)5M≡C(OEt)-C≡C—R 1 (M = Cr, W; R = Ph, tBu, SiMe3) readily add tertiary phosphanes PPhR2′ 4 (R′ = Ph, Me) to form stable zwitterionic phosphonium allenide complexes (CO)5M--C(OEt) = C≡C(R)-P+PhR2′ 5. Complex 5a (M = Cr, R = R′ = Ph) was characterized by X-ray diffraction. The addition of secondary phosphanes PHR2 6 to 1 affords red (2-phosphanyl ethenyl)-carbene complexes (CO)5M≡C(OEt)-CH≡C(R)-PR2 (E)-8 (R = tBu, cC6H11, Ph) in 34-89% isolated yields. Dinuclear complexes (CO)5M≡C(OEt)-CH≡C(R)-P(R2)M(CO)5 (E)-9 are obtained as byproducts. Compounds (E)-8b (M = Cr, R = cC6H11) and (E)-9i (M = Cr, R = Ph) were characterized by X-ray analyses.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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