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Results: 1-9 |
Results: 9
BETA-METALATION OF BRIDGED ALKENYL SULFONES - ACCESS TO A KEY INTERMEDIATE FOR EPIBATIDINE TOTAL SYNTHESIS
Authors: JONES CD SIMPKINS NS GIBLIN GMP
Citation: Cd. Jones et al., BETA-METALATION OF BRIDGED ALKENYL SULFONES - ACCESS TO A KEY INTERMEDIATE FOR EPIBATIDINE TOTAL SYNTHESIS, Tetrahedron letters, 39(9), 1998, pp. 1021-1022
ASYMMETRIC-SYNTHESIS OF EPIBATIDINE BY USE OF A NOVEL ENANTIOSELECTIVE SULFINATE ELIMINATION-REACTION
Authors: JONES CD SIMPKINS NS GIBLIN GMP
Citation: Cd. Jones et al., ASYMMETRIC-SYNTHESIS OF EPIBATIDINE BY USE OF A NOVEL ENANTIOSELECTIVE SULFINATE ELIMINATION-REACTION, Tetrahedron letters, 39(9), 1998, pp. 1023-1024
A CONCISE STEREOSELECTIVE SYNTHESIS OF EPIBATIDINE EMPLOYING CONJUGATE ADDITION TO AN ALKENYL SULFONE INTERMEDIATE AS THE KEY STEP
Authors: GIBLIN GMP JONES CD SIMPKINS NS
Citation: Gmp. Giblin et al., A CONCISE STEREOSELECTIVE SYNTHESIS OF EPIBATIDINE EMPLOYING CONJUGATE ADDITION TO AN ALKENYL SULFONE INTERMEDIATE AS THE KEY STEP, Synlett, (5), 1997, pp. 589
AMINO-ACID DERIVED THIANE OXIDE AND DIOXIDE SYSTEMS AS DISPOSABLE TEMPLATES - SYNTHESIS OF ALPHA-AMINO KETONES, ANTI-AMINO ALCOHOLS AND AN AMINO CYCLOPENTENONE
Authors: GAMBLE MP GIBLIN GMP MONTANA JG OBRIEN P OCKENDON TP TAYLOR RJK
Citation: Mp. Gamble et al., AMINO-ACID DERIVED THIANE OXIDE AND DIOXIDE SYSTEMS AS DISPOSABLE TEMPLATES - SYNTHESIS OF ALPHA-AMINO KETONES, ANTI-AMINO ALCOHOLS AND AN AMINO CYCLOPENTENONE, Tetrahedron letters, 37(41), 1996, pp. 7457-7460
AMINO-ACID DERIVED SULFONES FOR CHIRAL CYCLOPENTANE SYNTHESIS
Authors: GAMBLE MP GIBLIN GMP TAYLOR RJK
Citation: Mp. Gamble et al., AMINO-ACID DERIVED SULFONES FOR CHIRAL CYCLOPENTANE SYNTHESIS, Synlett, (7), 1995, pp. 779-780
DISCOVERY OF AN ORALLY BIOAVAILABLE NK1 RECEPTOR ANTAGONIST, -TETRAZOL-1-YLBENZYL)(2-PHENYLPIPERIDIN-3-YL)AMINE (GR203040), WITH POTENT ANTIEMETIC ACTIVITY
Authors: WARD P ARMOUR DR BAYS DE EVANS B GIBLIN GMP HERON N HUBBARD T LIANG K MIDDLEMISS D MORDAUNT J NAYLOR A PEGG NA VINADER MV WATSON SP BOUNTRA C EVANS DC
Citation: P. Ward et al., DISCOVERY OF AN ORALLY BIOAVAILABLE NK1 RECEPTOR ANTAGONIST, -TETRAZOL-1-YLBENZYL)(2-PHENYLPIPERIDIN-3-YL)AMINE (GR203040), WITH POTENT ANTIEMETIC ACTIVITY, Journal of medicinal chemistry, 38(26), 1995, pp. 4985-4992
SYNTHESIS OF NOVEL MONOCYCLIC SQUALESTATIN ANALOGS AS POTENTIAL INHIBITORS OF SQUALENE SYNTHASE
Authors: SHAW RE BURGESS C COUSINS RPC GIBLIN GMP LIVERMORE DGH SHINGLER AH SMITH C YOUDS PM
Citation: Re. Shaw et al., SYNTHESIS OF NOVEL MONOCYCLIC SQUALESTATIN ANALOGS AS POTENTIAL INHIBITORS OF SQUALENE SYNTHASE, Bioorganic & medicinal chemistry letters, 4(18), 1994, pp. 2155-2160
SEMISYNTHETIC SQUALESTATINS - SQUALENE SYNTHASE INHIBITION AND ANTIFUNGAL ACTIVITY - THE SAR OF C6 AND C7 MODIFICATIONS
Authors: GIBLIN GMP BELL R HANCOCK AP HARTLEY CD INGLIS GGA PAYNE JJ PROCOPIOU PA SHINGLER AH SMITH C SPOONER SJ
Citation: Gmp. Giblin et al., SEMISYNTHETIC SQUALESTATINS - SQUALENE SYNTHASE INHIBITION AND ANTIFUNGAL ACTIVITY - THE SAR OF C6 AND C7 MODIFICATIONS, Bioorganic & medicinal chemistry letters, 3(12), 1993, pp. 2605-2610
STRUCTURALLY SIMPLIFIED SQUALESTATINS - A CONVENIENT ROUTE TO A 6,7-UNSUBSTITUTED DERIVATIVE
Authors: LESTER MG GIBLIN GMP INGLIS GGA PROCOPIOU PA ROSS BC WATSON NS
Citation: Mg. Lester et al., STRUCTURALLY SIMPLIFIED SQUALESTATINS - A CONVENIENT ROUTE TO A 6,7-UNSUBSTITUTED DERIVATIVE, Tetrahedron letters, 34(27), 1993, pp. 4357-4360
Risultati: 1-9 |