Free Access
Issue
Med Sci (Paris)
Volume 17, Number 11, Novembre 2001
Page(s) 1230 - 1232
Section Prix Nobel 2001
DOI https://doi.org/10.1051/medsci/200117111230
Published online 15 November 2001
  1. Knowles WS, Sabacky MJ. Catalytic asymmetric hydrogenation employing a soluble, optically active, rhodium catalyst. J Chem Soc Chem Commun 1968 : 1445–6. [Google Scholar]
  2. Knowles WS, Sabacky MJ, Vineyard BDJ. Catalytic asymmetric hydrogenation. Ann NY Acad Sci 1973; 214 : 119–24. [Google Scholar]
  3. Miyashita A, Yasuda A, Takaya H, et al. Synthesis of 2,2’-bis(diphenylphosphino)-1,1’-binapthyl(BINAP) an atropisomeric chiral bis triarylphosphine and its use in the Rh(I)-catalyzed asymmetric hydrogeantion of α(acylamino)acrylic acid. J Am Chem Soc 1980; 102 : 7932–4. [Google Scholar]
  4. Noyori R. in «Asymmetric Catalysis in Organic Synthesis » John Wiley and Sons, Inc., New York, 1994. [Google Scholar]
  5. Katsuki T, Sharpless KB. The first pratical method for asymmetric epoxydation. J Am Chem Soc 1980; 102 : 5975–6. [Google Scholar]
  6. Kagan HB, Dang TP. Asymmmetric catalytic reduction with transition metal complexes. I A catalytic system of Rhodium (I) with (–) 2,3-O-isopropylidene-2,3-dihydroxy-1,4-bis-(diphenylphosphino)butane, a new chiral diphosphine. J Am Chem Soc 1972; 94 : 6429–33. [Google Scholar]

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