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  • Group 5  (1)
  • Methylenespiropentane  (1)
  • Wiley-Blackwell  (2)
  • American Chemical Society
  • 1995-1999  (2)
Collection
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  • Wiley-Blackwell  (2)
  • American Chemical Society
Years
  • 1995-1999  (2)
Year
  • 1
    ISSN: 1434-1948
    Keywords: Niobium ; Tin ; Hydrides ; Group 5 ; Group 14 ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of niobocene trihydride [Cp2NbH3] with one equivalent of an alkyl- or aryltin halide XnSnR4-n (n = 1, 2) leads to products of the displacement of hydride by tin, i.e. [Cp2NbH2(SnX3-nRn)] [R = Me, n = 3 (1); R = Me, × = Cl, n = 2 (3); R = Ph, n = 3 (4); R = Ph, × = Cl, n = 2 (5); R = Et, × = Br, n = 2 (6)]. Use of an excess of the tin reagent results in a halodealkylation exchange reaction at the tin atom bound to the metal center. Reaction of the mono(silyl) complexes [Cp2NbH2(SiXMe2)] (X = Cl, Ph) with organotin halides XnSnR4-n gives products of the displacement of silicon by tin, whereas the bis(silyl) complex [Cp2NbH(SiPhMe2)2] does not undergo this reaction. The bis(tin)-substituted niobocene [Cp2NbH(SnMe3)2] has been prepared by the reaction of [Cp2NbH2(SnMe3)] with the tin amide Me3SnNMe2 under thermal conditions, as well as by the literature method of thermolysis of [Cp2NbH(η2-C2H3Ph)] in the presence of Me3SnH. Reaction of [Cp2NbH(SnMe3)2] with two equivalents of Cl2SnMe2 affords the bis(tin)-substituted complex [Cp2NbH(SnClMe2)2] (9). The possible presence of non-classical hypervalent H···Sn-Cl interactions in this compound has been assessed by means of X-ray structure analysis. The structural data for 9 are in accord with an essentially classical description as a tin-substituted dihydride complex without significant Sn···H interactions.
    Additional Material: 1 Ill.
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  • 2
    ISSN: 1434-193X
    Keywords: Amino acids ; Bicyclopropylidene ; Methylenespiropentane ; Spiro compounds ; Organolithium derivatives ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Racemic bicyclopropylidenyl- (rac-11) and methylenespiropentyl- (rac-17) substituted alanines have been synthesized by iodination of bicyclopropylidenyl- and methylenespiropentylmethanols 7, 13, nucleophilic substitution of the iodine in 8, 14 with the enolate of ethyl α-(diphenylmethyleneamino)acetate (O'Donnell's glycine equivalent) and deprotection of 9, 15 in 24 and 18% overall yield, respectively. N-Methylbicyclopropylidenylalanine rac-22, was obtained from the Michael adduct of (bicyclopropylidenyl)magnesium bromide 18 to enamine 19 and deprotection of the carbamate 20 (23% overall yield). Racemic (1-amino-2-methylenespiropentane)- (37), (1-amino-2-methylenecyclopropane)- (3), and (1-aminobicyclopropylidene)carboxylic acid (39) were prepared as hydrochlorides by tert-butoxycarbonylation of the lithiated methylenespiropentane (6), methylenecyclopropane (4), or bicyclopropylidene (5) intermediates with di-tert-butyl pyrocarbonate (Boc2O), repeated lithiation of the tert-butyl esters 29, 30, and 33 with LDA and subsequent carboxylation, Curtius degradation of the half esters 31, 32, and 34 followed by deprotection in 11, 45, and 4% overall yields, respectively. Compound 37 was also prepared from bicyclopropylidene (5) following the same procedure, but with rearrangement in the last but one step, in 19% overall yield. An attempted Hofmann degradation of the bicyclopropylidenecarboxamido ester 40 with NBS failed and gave only bromohydrin 44 (27%), but with bis(acetoxy)iodobenzene provided carbamate 46a, b in 76 amd 79% yield, respectively. Along this route with subsequent deprotection of 46b, the amino acid 39 could be prepared in up to 10% overall yield from bicyclopropylidene.
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