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1999 carbohydrates carbohydrates U 0500 44 - 228 Ring Closing Metathesis of Sterically Hindered 1,6-Dienes: A New Approach to 5-Membered Branched Cyclitols. The sterically hindered carbohydrate derived 1,6-diene (III) undergoes efficient ring-closing metathesis using Schrock’s catalyst. The product can be readily converted to the 5-membered branched cyclitols (VIII) and (IX). — (SELLIER, ODILE; VAN DE WEGHE, PIERRE; EUSTACHE, JACQUES; Tetrahedron Lett. 40 (1999) 32, 5859-5860; Lab. Synth. Org. Chim. Microb., CNRS, Ec. Natl. Super. Chim., Univ. Haute-Alsace, F-68093 Mulhouse, Fr.; EN) 1

ChemInform Abstract: Ring Closing Metathesis of Sterically Hindered 1,6-Dienes: A New Approach to 5-Membered Branched Cyclitols

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1999 carbohydrates

carbohydratesU 0500

44 - 228Ring Closing Metathesis of Sterically Hindered 1,6-Dienes: A NewApproach to 5-Membered Branched Cyclitols. — The stericallyhindered carbohydrate derived 1,6-diene (III) undergoes efficient ring-closingmetathesis using Schrock’s catalyst. The product can be readily converted tothe 5-membered branched cyclitols (VIII) and (IX). — (SELLIER, ODILE;VAN DE WEGHE, PIERRE; EUSTACHE, JACQUES; Tetrahedron Lett. 40(1999) 32, 5859-5860; Lab. Synth. Org. Chim. Microb., CNRS, Ec. Natl.Super. Chim., Univ. Haute-Alsace, F-68093 Mulhouse, Fr.; EN)

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