Asymetryczna aminohydroksylacja Sharplessa (Polish Wikipedia)

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  • K. Barry Sharpless, Donald W. Patrick, Larry K. Truesdale, Scott A. Biller. New reaction. Stereospecific vicinal oxyamination of olefins by alkyl imido osmium compounds. „J. Am. Chem. Soc.”. 97 (8), s. 2305–2307, 1975. DOI: 10.1021/ja00841a071. 
  • Eugenio Herranz, Scott A. Biller, K. Barry Sharpless. Osmium-catalyzed vicinal oxyamination of olefins by N-chloro-N-argentocarbamates. „J. Am. Chem. Soc.”. 100 (11), s. 3596–3598, 1978. DOI: 10.1021/ja00479a051. 
  • S. C. Bergmeier. The Synthesis of Vicinal Amino Alcohols. „Tetrahedron”. 56 (17), s. 2561-2576, 2000. DOI: 10.1016/S0040-4020(00)00149-6. 
  • Peter O'Brien. Sharpless Asymmetric Aminohydroxylation: Scope, Limitations, and Use in Synthesis. „Angewandte Chemie International Edition”. 38 (3), s. 326-329, 1999. DOI: 10.1002/(SICI)1521-3773(19990201)38:3%3C326::AID-ANIE326%3E3.0.CO;2-T. 
  • J. A. Bodkin, M. D. McLeod. The Sharpless asymmetric aminohydroxylation. „J. Chem. Soc., Perkin Trans. 1”, s. 2733–2746, 2002. DOI: 10.1039/b111276g. 
  • Guigen Li, Hubert H. Angert, K. Barry Sharpless. N-Halocarbamate Salts Lead to More Efficient Catalytic Asymmetric Aminohydroxylation. „Angew. Chem. Int. Ed. Engl.”. 35 (23-24), s. 2813–2817, 1996. DOI: 10.1002/anie.199628131. 
  • C. Kolb, Michael S. VanNieuwenhze, K. Barry Sharpless. Catalytic Asymmetric Dihydroxylation. „Chem. Rev.”. 94 (8), s. 2483–2547, 1994. DOI: 10.1021/cr00032a009. 
  • Wallace Pringle, K. Barry Sharpless. The osmium-catalyzed aminohydroxylation of Baylis-Hillman olefins. „Tetrahedron Letters”. 40 (28), s. 5151-5154, 1999. DOI: 10.1016/S0040-4039(99)00887-4. 
  • Valery V. Fokin, K. Barry Sharpless. A Practical and Highly Efficient Aminohydroxylation of Unsaturated Carboxylic Acids. „Angew. Chem. Int. Ed. Engl.”. 40 (18), s. 3455–3457, 2001. DOI: 10.1002/1521-3773(20010917)40:18%3C3455::AID-ANIE3455%3E3.0.CO;2-I. 
  • A. Erik Rubin, K. Barry Sharpless. A Highly Efficient Aminohydroxylation Process. „Angew. Chem. Int. Ed. Engl.”. 36 (23), s. 2637–2640, 1997. DOI: 10.1002/anie.199726371. 
  • Joachim Rudolph, Peter C. Sennhenn, Cornelis P. Vlaar, K. Barry Sharpless. Smaller Substituents on Nitrogen Facilitate the Osmium-Catalyzed Asymmetric Aminohydroxylation. „Angew. Chem. Int. Ed. Engl.”. 35 (23-24), s. 2810–2813, 1996. DOI: 10.1002/anie.199628101. 
  • Hyunsoo Han, Chang-Woo Cho, Kim D. Janda. A Substrate-Based Methodology That Allows the Regioselective Control of the Catalytic Aminohydroxylation Reaction. „Chem. Eur. J.”. 5 (5), s. 1565–1569, 1999. DOI: 10.1002/(SICI)1521-3765(19990503)5:5%3C1565::AID-CHEM1565%3E3.0.CO;2-J. 
  • Jong-Cheol Lee, Geun Tae Kim, Young Key Shim, Sung Ho Kang. An asymmetric aminohydroxylation approach to the stereoselective synthesis of cis-substituted azetidinone of loracarbef. „Tetrahedron Letters”. 42 (27), s. 4519–4521, 2001. DOI: 10.1016/S0040-4039(01)00757-2. 
  • M. Bruncko, G. Schingloff, K. B. Sharpless. N-Bromoacetamide—A New Nitrogen Source for the Catalytic Asymmetric Aminohydroxylation of Olefins. „Angew. Chem. Int. Ed. Engl.”. 36 (13-14), s. 1483-1486, 1997. DOI: 10.1002/anie.199714831. 

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