cheminform abstract: diastereoselective ring opening of limonene oxide with water catalyzed by...

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1999 terpenes terpenes U 0200 39 - 160 Diastereoselective Ring Opening of Limonene Oxide with Water Catalyzed by β-Ketophosphonate Complexes of Molybdenum(VI). The hydrolytic ring opening of limonene oxides (I) and (II) in the presence of chiral camphor ketophosphonate derived Mo-complexes such as (III) is investigated. The cis-isomer (I) is readily converted to the diol, whereas the trans isomer (II) remains unreacted, thus providing a method for the kinetic separation of the trans diastereomer. — (SALLES, LAURENT; NIXON, AN- DREW F.; RUSSELL, NICHOLAS C.; CLARKE, RUSSELL; POGORZELEC, PETER; COLE-HAMILTON, DAVID J.; Tetrahedron: Asymmetry 10 (1999) 8, 1471-1476; Sch. Chem., Cent. Biomol. Sci., Univ. St. Andrews, St. Andrews, Fife KY16 9ST, UK; EN) 1

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1999 terpenes

terpenesU 0200

39 - 160Diastereoselective Ring Opening of Limonene Oxide with WaterCatalyzed by β-Ketophosphonate Complexes of Molybdenum(VI).— The hydrolytic ring opening of limonene oxides (I) and (II) in the presenceof chiral camphor ketophosphonate derived Mo-complexes such as (III) isinvestigated. The cis-isomer (I) is readily converted to the diol, whereas thetrans isomer (II) remains unreacted, thus providing a method for the kineticseparation of the trans diastereomer. — (SALLES, LAURENT; NIXON, AN-DREW F.; RUSSELL, NICHOLAS C.; CLARKE, RUSSELL; POGORZELEC,PETER; COLE-HAMILTON, DAVID J.; Tetrahedron: Asymmetry 10 (1999) 8,1471-1476; Sch. Chem., Cent. Biomol. Sci., Univ. St. Andrews, St. Andrews,Fife KY16 9ST, UK; EN)

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