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An Approach toward the Illudin Family of Sesquiterpenes Using the Tandem Cyclization−Cycloaddition Reaction of Rhodium Carbenoids

Journal of organic chemistry, 1997-03, Vol.62 (5), p.1317-1325

1997

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Resistance to beta-lactam antibiotics: structure and mechanism based design of beta-lactamase inhibitors

Current medicinal chemistry, 2002-06, Vol.9 (12), p.1145-1165

2002

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Spirocyclopropyl β-Lactams as Mechanism-Based Inhibitors of Serine β-Lactamases. Synthesis by Rhodium-Catalyzed Cyclopropanation of 6-Diazopenicillanate Sulfone

Journal of medicinal chemistry, 2003-06, Vol.46 (13), p.2569-2571

2003

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Generation and Cycloaddition Behavior of Spirocyclic Carbonyl Ylides. Application to the Synthesis of the Pterosin Family of Sesquiterpenes

Journal of organic chemistry, 1996-01, Vol.61 (1), p.73-81

1996

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Synthesis and Structure−Activity Relationship of N-Substituted 4-Arylsulfonylpiperidine-4-hydroxamic Acids as Novel, Orally Active Matrix Metalloproteinase Inhibitors for the Treatment of Osteoarthritis

Journal of medicinal chemistry, 2003-06, Vol.46 (12), p.2376-2396

2003

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Dipolar Cycloaddition of Novel 6-(Nitrileoxidomethyl) Penam Sulfone: An Efficient Route to a New Class of β-Lactamase Inhibitors

Organic letters, 2000-10, Vol.2 (20), p.3087-3090

2000

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Abstract 5412: Expression and inhibition of monocarboxylate transporters in canine osteosarcoma

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.5412-5412

2017

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Synthetic studies toward Illudins and Ptaquilosin. A highly convergent approach via the dipolar cycloaddition of carbonyl ylides

Journal of the American Chemical Society, 1994-03, Vol.116 (6), p.2667-2668

1994

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An efficient method to prepare α-sulfonyl hydroxamic acid derivatives

Tetrahedron letters, 2001-07, Vol.42 (28), p.4605-4607

2001

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Allyl and propargyl substituted penam sulfones as versatile intermediates toward the syntheses of new β-lactamase inhibitors

Bioorganic & medicinal chemistry letters, 2001-04, Vol.11 (8), p.997-1000

2001

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Studies on Intramolecular Higher-Order Cycloaddition Reactions

Journal of organic chemistry, 1996-02, Vol.61 (3), p.842-850

1996

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An efficient dipolar-cycloaddition route to the pterosin family of sesquiterpenes

Tetrahedron letters, 1995-03, Vol.36 (12), p.1989-1992

1995

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Corrigendum to “allyl and Propargyl substituted penam sulfones as versatile intermediates toward the syntheses of new β-lactamase inhibitors”

Bioorganic & medicinal chemistry letters, 2001-07, Vol.11 (14), p.1963

2001

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Intramolecular chromium(0) promoted higher-order cycloaddition reactions

Tetrahedron letters, 1993-02, Vol.34 (6), p.935-938

1993

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Synthetic studies on ingenane diterpenes; intermolecular and transition metal-mediated intramolecular higher-order cycloaddition reactions

Sandanayaka, Vincent P

1993

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ChemInform Abstract: Dipolar Cycloaddition of Novel 6-(Nitrileoxidomethyl) Penam Sulfone: An Efficient Route to a New Class of β-Lactamase Inhibitors

ChemInform, 2001-01, Vol.32 (5), p.no-no

2001

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ChemInform Abstract: An Efficient Method to Prepare α-Sulfonyl Hydroxamic Acid Derivatives

ChemInform, 2001-10, Vol.32 (40), p.no-no

2001

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ChemInform Abstract: Allyl and Propargyl Substituted Penam Sulfones as Versatile Intermediates Toward the Syntheses of New β-Lactamase Inhibitors

ChemInform, 2001-08, Vol.32 (32), p.no-no

2001

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Establishment of Mastrus ridens (Hymenoptera: Ichneumonidae), an ectoparasitoid of codling moth, in New Zealand

Proceedings of the 5th International Symposium on Biological Control of Arthropods, Langkawi, Malaysia, September 11-15, 2017, 2017, p.85-87

2017

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An Approach toward the Illudin Family of Sesquiterpenes Using the Tandem Cyclization−Cycloaddition Reaction of Rhodium Carbenoids

Resistance to beta-lactam antibiotics: structure and mechanism based design of beta-lactamase inhibitors

Spirocyclopropyl β-Lactams as Mechanism-Based Inhibitors of Serine β-Lactamases. Synthesis by Rhodium-Catalyzed Cyclopropanation of 6-Diazopenicillanate Sulfone

Generation and Cycloaddition Behavior of Spirocyclic Carbonyl Ylides. Application to the Synthesis of the Pterosin Family of Sesquiterpenes

Synthesis and Structure−Activity Relationship of N-Substituted 4-Arylsulfonylpiperidine-4-hydroxamic Acids as Novel, Orally Active Matrix Metalloproteinase Inhibitors for the Treatment of Osteoarthritis

Dipolar Cycloaddition of Novel 6-(Nitrileoxidomethyl) Penam Sulfone: An Efficient Route to a New Class of β-Lactamase Inhibitors

Abstract 5412: Expression and inhibition of monocarboxylate transporters in canine osteosarcoma

Synthetic studies toward Illudins and Ptaquilosin. A highly convergent approach via the dipolar cycloaddition of carbonyl ylides

An efficient method to prepare α-sulfonyl hydroxamic acid derivatives

Allyl and propargyl substituted penam sulfones as versatile intermediates toward the syntheses of new β-lactamase inhibitors

Studies on Intramolecular Higher-Order Cycloaddition Reactions

An efficient dipolar-cycloaddition route to the pterosin family of sesquiterpenes

Corrigendum to “allyl and Propargyl substituted penam sulfones as versatile intermediates toward the syntheses of new β-lactamase inhibitors”

Intramolecular chromium(0) promoted higher-order cycloaddition reactions

Synthetic studies on ingenane diterpenes; intermolecular and transition metal-mediated intramolecular higher-order cycloaddition reactions

ChemInform Abstract: Dipolar Cycloaddition of Novel 6-(Nitrileoxidomethyl) Penam Sulfone: An Efficient Route to a New Class of β-Lactamase Inhibitors

ChemInform Abstract: An Efficient Method to Prepare α-Sulfonyl Hydroxamic Acid Derivatives

ChemInform Abstract: Allyl and Propargyl Substituted Penam Sulfones as Versatile Intermediates Toward the Syntheses of New β-Lactamase Inhibitors

Establishment of Mastrus ridens (Hymenoptera: Ichneumonidae), an ectoparasitoid of codling moth, in New Zealand

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