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An evaluation of vitamin E and pycnogenol in children suffering from oral mucositis during cancer chemotherapy

Oral diseases, 2013-07, Vol.19 (5), p.456-464

2013

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Mutations conferring resistance to SCH6, a novel hepatitis C virus NS3/4A protease inhibitor. Reduced RNA replication fitness and partial rescue by second-site mutations

The Journal of biological chemistry, 2006-03, Vol.281 (12), p.8205-8215

2006

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A comparative evaluation of intranasal midazolam, ketamine and their combination for sedation of young uncooperative pediatric dental patients: a triple blind randomized crossover trial

The Journal of clinical pediatric dentistry, 2011-07, Vol.35 (4), p.415-420

2011

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A comparative evaluation of drops versus atomized administration of intranasal ketamine for the procedural sedation of young uncooperative pediatric dental patients: a prospective crossover trial

The Journal of clinical pediatric dentistry, 2011-09, Vol.36 (1), p.79-84

2011

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Discovery of SCH446211 (SCH6): A New Ketoamide Inhibitor of the HCV NS3 Serine Protease and HCV Subgenomic RNA Replication

Journal of medicinal chemistry, 2006-05, Vol.49 (9), p.2750-2757

2006

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Midazolam-fentanyl analgo-sedation in pediatric dental patients--a pilot study

The Journal of clinical pediatric dentistry, 2010-09, Vol.35 (1), p.105-110

2010

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A comparative evaluation of agents producing analgo-sedation in pediatric dental patients

The Journal of clinical pediatric dentistry, 2009-12, Vol.34 (2), p.183-188

2009

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Hydroxylated analogues of the orally active broad spectrum antifungal, Sch 51048 ( 1), and the discovery of posaconazole [Sch 56592; 2 or ( S, S)- 5]

Bioorganic & medicinal chemistry letters, 2006, Vol.16 (1), p.186-190

2006

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Solution- and solid-phase synthesis of enantiomerically pure spiro oxindoles

Tetrahedron letters, 2002-12, Vol.43 (49), p.8981-8983

2002

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Hepatitis C virus NS3-4A serine protease inhibitors: Use of a P 2–P 1 cyclopropyl alanine combination for improved potency

Bioorganic & medicinal chemistry letters, 2005-10, Vol.15 (20), p.4515-4519

2005

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[3+2] Cycloaddition of trimethylenemethane (TMM) to α,β-unsaturated γ-lactam. Preparation of 5,5-fused proline surrogates

Tetrahedron letters, 2003-06, Vol.44 (27), p.5033-5035

2003

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Enantioselective syntheses of carbocyclic ribavirin and its analogs: linear versus convergent approaches

Tetrahedron letters, 2000, Vol.41 (49), p.9575-9579

2000

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Novel inhibitors of the hepatitis C virus NS3 proteinase

Bioorganic & medicinal chemistry letters, 2005-10, Vol.15 (19), p.4275-4278

2005

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Multiple-stage mass spectrometric analysis of complex oligosaccharide antibiotics (everninomicins) in a quadrupole ion trap

Journal of the American Society for Mass Spectrometry, 2002-11, Vol.13 (11), p.1313-1321

2002

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An unusual acetonide group migration

Tetrahedron letters, 2003-09, Vol.44 (38), p.7201-7204

2003

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Concise asymmetric routes to 2,2,4-trisubstituted tetrahydrofurans via chiral titanium imide enolates: Key intermediates towards synthesis of highly active azole antifungals SCH 51048 and SCH 56592

Tetrahedron letters, 1996-08, Vol.37 (32), p.5657-5660

1996

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Chemical modifications and structure activity studies of ziracin and related everninomicin antibiotics

Bioorganic & medicinal chemistry letters, 1999-04, Vol.9 (8), p.1209-1214

1999

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Synthesis and antifungal activity of the 2,2,5-tetrahydrofuran regioisomers of SCH 51048

Bioorganic & medicinal chemistry letters, 2002-07, Vol.12 (13), p.1739-1742

2002

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DETERMINATION OF THE ABSOLUTE STEREOCHEMISTRY AT THE C16 ORTHOESTER OF EVERNINOMICIN ANTIBIOTICS; A NOVEL ACID-CATALYZED ISOMERIZATION OF ORTHOESTERS

Tetrahedron letters, 1997-11, Vol.38 (46), p.7989-7992

1997

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Recent studies on veratrum alkaloids: a new reaction of sodium triacetoxyborohydride [NaBH(OAc) 3]

Tetrahedron letters, 1983, Vol.24 (3), p.273-276

1983

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Structure elucidation of everninomicin-6, a new oligosaccharide antibiotic, by chemical degradation and FAB-MS methods

Journal of the American Society for Mass Spectrometry, 1997-11, Vol.8 (11), p.1134-1140

1997

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Total synthesis of the antifungal cyclic depsipeptides Sch 57697 and aureobasidin A

Tetrahedron letters, 1996-08, Vol.37 (32), p.5661-5664

1996

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Total synthesis and absolute stereochemistry of the antifungal dipeptide Sch 37137 and its 2S,3S-isomer

Tetrahedron letters, 1993-05, Vol.34 (20), p.3201-3204

1993

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Structure elucidation of Sch 49088, a novel everninomicin antibiotic containing an unusual hydroxylamino-ether sugar, everhydroxylaminose

Tetrahedron letters, 1998-11, Vol.39 (46), p.8441-8444

1998

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Structural Characterization of the Oligosaccharide Antibiotics Everninomicins by Negative Ion FAB and ESI/MS

The Journal of Antibiotics, 2000/06/25, Vol.53(6), pp.640-643

2000

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An evaluation of vitamin E and pycnogenol in children suffering from oral mucositis during cancer chemotherapy

Mutations conferring resistance to SCH6, a novel hepatitis C virus NS3/4A protease inhibitor. Reduced RNA replication fitness and partial rescue by second-site mutations

A comparative evaluation of intranasal midazolam, ketamine and their combination for sedation of young uncooperative pediatric dental patients: a triple blind randomized crossover trial

A comparative evaluation of drops versus atomized administration of intranasal ketamine for the procedural sedation of young uncooperative pediatric dental patients: a prospective crossover trial

Discovery of SCH446211 (SCH6): A New Ketoamide Inhibitor of the HCV NS3 Serine Protease and HCV Subgenomic RNA Replication

Midazolam-fentanyl analgo-sedation in pediatric dental patients--a pilot study

A comparative evaluation of agents producing analgo-sedation in pediatric dental patients

Hydroxylated analogues of the orally active broad spectrum antifungal, Sch 51048 ( 1), and the discovery of posaconazole [Sch 56592; 2 or ( S, S)- 5]

Solution- and solid-phase synthesis of enantiomerically pure spiro oxindoles

Hepatitis C virus NS3-4A serine protease inhibitors: Use of a P 2–P 1 cyclopropyl alanine combination for improved potency

[3+2] Cycloaddition of trimethylenemethane (TMM) to α,β-unsaturated γ-lactam. Preparation of 5,5-fused proline surrogates

Enantioselective syntheses of carbocyclic ribavirin and its analogs: linear versus convergent approaches

Novel inhibitors of the hepatitis C virus NS3 proteinase

Multiple-stage mass spectrometric analysis of complex oligosaccharide antibiotics (everninomicins) in a quadrupole ion trap

An unusual acetonide group migration

Concise asymmetric routes to 2,2,4-trisubstituted tetrahydrofurans via chiral titanium imide enolates: Key intermediates towards synthesis of highly active azole antifungals SCH 51048 and SCH 56592

Chemical modifications and structure activity studies of ziracin and related everninomicin antibiotics

Synthesis and antifungal activity of the 2,2,5-tetrahydrofuran regioisomers of SCH 51048

DETERMINATION OF THE ABSOLUTE STEREOCHEMISTRY AT THE C16 ORTHOESTER OF EVERNINOMICIN ANTIBIOTICS; A NOVEL ACID-CATALYZED ISOMERIZATION OF ORTHOESTERS

Recent studies on veratrum alkaloids: a new reaction of sodium triacetoxyborohydride [NaBH(OAc) 3]

Structure elucidation of everninomicin-6, a new oligosaccharide antibiotic, by chemical degradation and FAB-MS methods

Total synthesis of the antifungal cyclic depsipeptides Sch 57697 and aureobasidin A

Total synthesis and absolute stereochemistry of the antifungal dipeptide Sch 37137 and its 2S,3S-isomer

Structure elucidation of Sch 49088, a novel everninomicin antibiotic containing an unusual hydroxylamino-ether sugar, everhydroxylaminose

Structural Characterization of the Oligosaccharide Antibiotics Everninomicins by Negative Ion FAB and ESI/MS

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