ACS Publications: High Quality, High Impact

Top 10 Most-Accessed Articles in 2006 from ACS Legacy Archives

  1. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds
    Norio Miyaura, Akira Suzuki
    Chem. Rev. 1995, 95(7), pp 2457-2483. DOI: cr00039a007
  2. Synthesis and characterization of nearly monodisperse CdE (E = sulfur, selenium, tellurium) semiconductor nanocrystallites
    C. B. Murray, D. J. Norris, M. G. Bawendi
    J. Am. Chem. Soc. 1993, 115(19), pp 8706-8715. DOI: ja00072a025
  3. A new family of mesoporous molecular sieves prepared with liquid crystal templates
    J. S. Beck, J. C. Vartuli, W. J. Roth, M. E. Leonowicz, C. T. Kresge, K. D. Schmitt, C. T. W. Chu, D. H. Olson, E. W. Sheppard, and et al.
    J. Am. Chem. Soc, 1992, 114(27), pp 10834-10843. DOI: ja00053a020
  4. Catalytic Asymmetric Dihydroxylation
    Hartmuth C. Kolb, Michael S. VanNieuwenhze, K. Barry Sharpless
    Chem. Rev. 1994, 94(8), pp 2483-2547. DOI: cr00032a009
  5. Protection of hydroxyl groups as tert-butyldimethylsilyl derivatives
    E. J. Corey and A. Venkateswarlu
    J. Am. Chem. Soc. 1992, 94(17), pp 6190-6191. DOI: ja00772a043
  6. Rapid chromatographic technique for preparative separations with moderate resolution
    W. Clark Still, Michael Kahn, Abhijit Mitra
    J. Org. Chem. 1978, 43(14), pp 2923-2925. DOI: jo00408a041
  7. Conversion of light to electricity by cis-X2bis(2,2'-bipyridyl-4,4'-dicarboxylate)ruthenium(II) charge-transfer sensitizers (X = Cl-, Br-, I-, CN-, and SCN-) on nanocrystalline titanium dioxide electrodes
    M. K. Nazeeruddin, A. Kay, I. Rodicio, R. Humphry-Baker, E. Mueller, P. Liska, N. Vlachopoulos, and M. Graetzel
    J. Am. Chem. Soc. 1993, 115(14), pp 6382-6390. DOI: ja00067a063
  8. Environmental Applications of Semiconductor Photocatalysis
    Michael R. Hoffmann, Scot T. Martin, Wonyong Choi, and Detlef W. Bahnemann
    Chem. Rev. 1995, 95(1), pp 69-96. DOI: cr00033a004
  9. A useful 12-I-5 triacetoxyperiodinane (the Dess-Martin periodinane) for the selective oxidation of primary or secondary alcohols and a variety of related 12-I-5 species
    Daniel B. Dess and J. C. Martin
    J. Am. Chem. Soc. 1991, 113(19), pp 7277-7287. DOI: ja00019a027
  10. Readily accessible 12-I-5 oxidant for the conversion of primary and secondary alcohols to aldehydes and ketones
    D. B. Dess and J. C. Martin
    J. Org. Chem. 1983, 48(22), pp 4155-4156. DOI: jo00170a070

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