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Results: 1-11 |
Results: 11
OZONOLYSIS FOR THE PREPARATION OF HIGH OXIDATION-STATE TRANSITION-METAL COMPLEXES AND THE CRYSTAL-STRUCTURE OF [PPH4](2)[RU2O(MU-OCOET)(2)CL-6]
Authors: BAILEY AJ GRIFFITH WP MARSDEN SP WHITE AJP WILLIAMS DJ
Citation: Aj. Bailey et al., OZONOLYSIS FOR THE PREPARATION OF HIGH OXIDATION-STATE TRANSITION-METAL COMPLEXES AND THE CRYSTAL-STRUCTURE OF [PPH4](2)[RU2O(MU-OCOET)(2)CL-6], Journal of the Chemical Society. Dalton transactions (Print), (21), 1998, pp. 3673-3677
CHIRAL VINYL DIOXAZABOROCINES IN SYNTHESIS - ASYMMETRIC-SYNTHESIS OF 5-SUBSTITUTED DELTA-2-ISOXAZOLINES VIA NITRILE OXIDE CYCLOADDITION
Authors: DAVIES CD MARSDEN SP STOKES ESE
Citation: Cd. Davies et al., CHIRAL VINYL DIOXAZABOROCINES IN SYNTHESIS - ASYMMETRIC-SYNTHESIS OF 5-SUBSTITUTED DELTA-2-ISOXAZOLINES VIA NITRILE OXIDE CYCLOADDITION, Tetrahedron letters, 39(46), 1998, pp. 8513-8516
RHODIUM-CATALYZED REACTIONS OF SILYLATED DIAZOACETATES - STEREOSELECTIVE SYNTHESIS OF ALPHA-SILYLATED GAMMA-LACTONES VIA C-H INSERTION
Authors: MARSDEN SP PANG WK
Citation: Sp. Marsden et Wk. Pang, RHODIUM-CATALYZED REACTIONS OF SILYLATED DIAZOACETATES - STEREOSELECTIVE SYNTHESIS OF ALPHA-SILYLATED GAMMA-LACTONES VIA C-H INSERTION, Tetrahedron letters, 39(33), 1998, pp. 6077-6080
STEREOCONTROLLED POLYOL SYNTHESIS VIA C-H INSERTION REACTIONS OF SILICON TETHERED DIAZOACETATES
Authors: KABLEAN SN MARSDEN SP CRAIG AM
Citation: Sn. Kablean et al., STEREOCONTROLLED POLYOL SYNTHESIS VIA C-H INSERTION REACTIONS OF SILICON TETHERED DIAZOACETATES, Tetrahedron letters, 39(28), 1998, pp. 5109-5112
STEREOSELECTIVE SYNTHESIS OF 2,3,5-TRISUBSTITUTED TETRAHYDROFURANS BYAN ALLYL SILANE METATHESIS - NUCLEOPHILIC-ADDITION SEQUENCE
Authors: CASSIDY JH MARSDEN SP STEMP G
Citation: Jh. Cassidy et al., STEREOSELECTIVE SYNTHESIS OF 2,3,5-TRISUBSTITUTED TETRAHYDROFURANS BYAN ALLYL SILANE METATHESIS - NUCLEOPHILIC-ADDITION SEQUENCE, Synlett, (12), 1997, pp. 1411-1413
A NOVEL, STEREOCONTROLLED SYNTHESIS OF 1,2-TRANS-CYCLOPROPANES - CYCLOPROPYL BORONATE ESTERS AS PARTNERS IN SUZUKI COUPLINGS WITH ARYL HALIDES
Authors: HILDEBRAND JP MARSDEN SP
Citation: Jp. Hildebrand et Sp. Marsden, A NOVEL, STEREOCONTROLLED SYNTHESIS OF 1,2-TRANS-CYCLOPROPANES - CYCLOPROPYL BORONATE ESTERS AS PARTNERS IN SUZUKI COUPLINGS WITH ARYL HALIDES, Synlett, (9), 1996, pp. 893
APPLICATION OF GLYCALS TO THE SYNTHESIS OF OLIGOSACCHARIDES - CONVERGENT TOTAL SYNTHESES OF THE LEWIS-X TRISACCHARIDE SIALYL-LEWIS-X ANTIGENIC DETERMINANT AND HIGHER CONGENERS
Authors: DANISHEFSKY SJ GERVAY J PETERSON JM MCDONALD FE KOSEKI K GRIFFITH DA ORIYAMA T MARSDEN SP
Citation: Sj. Danishefsky et al., APPLICATION OF GLYCALS TO THE SYNTHESIS OF OLIGOSACCHARIDES - CONVERGENT TOTAL SYNTHESES OF THE LEWIS-X TRISACCHARIDE SIALYL-LEWIS-X ANTIGENIC DETERMINANT AND HIGHER CONGENERS, Journal of the American Chemical Society, 117(7), 1995, pp. 1940-1953
STUDIES TOWARDS THE TOTAL SYNTHESIS OF RAPAMYCIN - A CONVERGENT AND STEREOSELECTIVE SYNTHESIS OF THE C22-C32 CARBON FRAMEWORK
Authors: ANDERSON JC LEY SV MARSDEN SP
Citation: Jc. Anderson et al., STUDIES TOWARDS THE TOTAL SYNTHESIS OF RAPAMYCIN - A CONVERGENT AND STEREOSELECTIVE SYNTHESIS OF THE C22-C32 CARBON FRAMEWORK, Tetrahedron letters, 35(13), 1994, pp. 2087-2090
STUDIES TOWARDS THE TOTAL SYNTHESIS OF RAPAMYCIN - PREPARATION OF THECYCLOHEXYL C33-C42 FRAGMENT AND FURTHER COUPLING TO AFFORD THE C22-C42 CARBON UNIT
Authors: KOUKLOVSKY C LEY SV MARSDEN SP
Citation: C. Kouklovsky et al., STUDIES TOWARDS THE TOTAL SYNTHESIS OF RAPAMYCIN - PREPARATION OF THECYCLOHEXYL C33-C42 FRAGMENT AND FURTHER COUPLING TO AFFORD THE C22-C42 CARBON UNIT, Tetrahedron letters, 35(13), 1994, pp. 2091-2094
TETRAPROPYLAMMONIUM PERRUTHENATE, PR4N-, TPAP - A CATALYTIC OXIDANT FOR ORGANIC-SYNTHESIS(RUO4)
Authors: LEY SV NORMAN J GRIFFITH WP MARSDEN SP
Citation: Sv. Ley et al., TETRAPROPYLAMMONIUM PERRUTHENATE, PR4N-, TPAP - A CATALYTIC OXIDANT FOR ORGANIC-SYNTHESIS(RUO4), Synthesis, (7), 1994, pp. 639-666
STEREOSELECTIVE TOTAL SYNTHESES OF AMAUROMINE AND 5-N-ACETYLARDEEMIN - A CONCISE ROUTE TO TILE FAMILY OF REVERSE-PRENYLATED HEXAHYDROPYRROLOINDOLE ALKALOIDS
Authors: MARSDEN SP DEPEW KM DANISHEFSKY SJ
Citation: Sp. Marsden et al., STEREOSELECTIVE TOTAL SYNTHESES OF AMAUROMINE AND 5-N-ACETYLARDEEMIN - A CONCISE ROUTE TO TILE FAMILY OF REVERSE-PRENYLATED HEXAHYDROPYRROLOINDOLE ALKALOIDS, Journal of the American Chemical Society, 116(24), 1994, pp. 11143-11144
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