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Total Synthesis of Isokidamycin

Journal of the American Chemical Society, 2010-11, Vol.132 (44), p.15528-15530

2010

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Studies toward the syntheses of pluramycin natural products. The first total synthesis of isokidamycin

Tetrahedron, 2011-09, Vol.67 (35), p.6524-6538

2011

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Oxabicyclooctane-Linked Novel Bacterial Topoisomerase Inhibitors as Broad Spectrum Antibacterial Agents

ACS medicinal chemistry letters, 2014-05, Vol.5 (5), p.609-614

2014

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Tricyclic 1,5-naphthyridinone oxabicyclooctane-linked novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents-SAR of left-hand-side moiety (Part-2)

Bioorganic & medicinal chemistry letters, 2015-05, Vol.25 (9), p.1831-1835

2015

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Hydroxy tricyclic 1,5-naphthyridinone oxabicyclooctane-linked novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents-SAR of RHS moiety (Part-3)

Bioorganic & medicinal chemistry letters, 2015-06, Vol.25 (12), p.2473-2478

2015

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Structure activity relationship of C-2 ether substituted 1,5-naphthyridine analogs of oxabicyclooctane-linked novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents (Part-5)

Bioorganic & medicinal chemistry letters, 2015-09, Vol.25 (17), p.3630-3635

2015

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Structure activity relationship of pyridoxazinone substituted RHS analogs of oxabicyclooctane-linked 1,5-naphthyridinyl novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents (Part-6)

Bioorganic & medicinal chemistry letters, 2015-09, Vol.25 (17), p.3636-3643

2015

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Structure activity relationship of substituted 1,5-naphthyridine analogs of oxabicyclooctane-linked novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents (Part-4)

Bioorganic & medicinal chemistry letters, 2015-06, Vol.25 (11), p.2409-2415

2015

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Regioselective Synthesis of Unsymmetrical C-Aryl Glycosides Using Silicon Tethers as Disposable Linkers

Journal of the American Chemical Society, 2003-10, Vol.125 (43), p.12994-12995

2003

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General Strategies for the Synthesis of the Major Classes of C-Aryl Glycosides

Journal of the American Chemical Society, 2001-07, Vol.123 (28), p.6937-6938

2001

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Application of Ring-Closing Metathesis to the Formal Total Synthesis of (+)−FR900482

Journal of the American Chemical Society, 2000-11, Vol.122 (44), p.10781-10787

2000

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C1–C2-linker substituted 1,5-naphthyridine analogues of oxabicyclooctane-linked NBTIs as broad-spectrum antibacterial agents (part 7)

MedChemComm, 2015-01, Vol.6 (10), p.1773-1780

2015

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Total Synthesis of (+)-Ambruticin S

Journal of the American Chemical Society, 2001-12, Vol.123 (49), p.12432-12433

2001

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Extension of ASM3 for two-step nitrification and denitrification and its calibration and validation with batch tests and pilot scale data

Water research (Oxford), 2009-04, Vol.43 (6), p.1680-1692

2009

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General entries to C-aryl glycosides. Formal synthesis of galtamycinone

Tetrahedron letters, 2003-01, Vol.44 (5), p.1075-1077

2003

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4-Arylcyclohexylalanine analogs as potent, selective, and orally active inhibitors of dipeptidyl peptidase IV

Bioorganic & medicinal chemistry letters, 2007-11, Vol.17 (21), p.5806-5811

2007

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Structure activity relationship of N-1 substituted 1,5-naphthyrid-2-one analogs of oxabicyclooctane-linked novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents (Part-9)

Bioorganic & medicinal chemistry letters, 2022-11, Vol.75, p.128808, Article 128808

2022

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Explosible dusts, US codes and standards of safe management practices

Process safety progress, 2006-12, Vol.25 (4), p.298-302

2006

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A recent explosion protection system failure

Plant/operations progress, 2005-06, Vol.24 (2), p.126-129

Kaelin Sr, David E.

2005

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Modelling nitrite in wastewater treatment systems: a discussion of different modelling concepts

Water science and technology, 2008-01, Vol.58 (6), p.1155-1171

2008

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In Vitro and In Vivo Characterization of the Novel Oxabicyclooctane-Linked Bacterial Topoisomerase Inhibitor AM-8722, a Selective, Potent Inhibitor of Bacterial DNA Gyrase

Antimicrobial agents and chemotherapy, 2016-08, Vol.60 (8), p.4830-4839

2016

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Novel methodologies for the synthesis of C-aryl glycosides and progress toward the synthesis of the C-aryl glycoside natural products galtamycinone and kidamycin

Kaelin, David Earl

2002

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The future of the OSHA PSM standard

Occupational health & safety, 2014-07, Vol.83 (7), p.64

Kaelin, Sr, David E

2014

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ChemInform Abstract: 4-Arylcyclohexylalanine Analogues as Potent, Selective and Orally Active Inhibitors of Dipeptidyl Peptidase IV

ChemInform, 2008-02, Vol.39 (6), p.no-no

2008

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Total Synthesis of Isokidamycin

Studies toward the syntheses of pluramycin natural products. The first total synthesis of isokidamycin

Oxabicyclooctane-Linked Novel Bacterial Topoisomerase Inhibitors as Broad Spectrum Antibacterial Agents

Tricyclic 1,5-naphthyridinone oxabicyclooctane-linked novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents-SAR of left-hand-side moiety (Part-2)

Hydroxy tricyclic 1,5-naphthyridinone oxabicyclooctane-linked novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents-SAR of RHS moiety (Part-3)

Structure activity relationship of C-2 ether substituted 1,5-naphthyridine analogs of oxabicyclooctane-linked novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents (Part-5)

Structure activity relationship of pyridoxazinone substituted RHS analogs of oxabicyclooctane-linked 1,5-naphthyridinyl novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents (Part-6)

Structure activity relationship of substituted 1,5-naphthyridine analogs of oxabicyclooctane-linked novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents (Part-4)

Regioselective Synthesis of Unsymmetrical C-Aryl Glycosides Using Silicon Tethers as Disposable Linkers

General Strategies for the Synthesis of the Major Classes of C-Aryl Glycosides

Application of Ring-Closing Metathesis to the Formal Total Synthesis of (+)−FR900482

C1–C2-linker substituted 1,5-naphthyridine analogues of oxabicyclooctane-linked NBTIs as broad-spectrum antibacterial agents (part 7)

Total Synthesis of (+)-Ambruticin S

Extension of ASM3 for two-step nitrification and denitrification and its calibration and validation with batch tests and pilot scale data

General entries to C-aryl glycosides. Formal synthesis of galtamycinone

4-Arylcyclohexylalanine analogs as potent, selective, and orally active inhibitors of dipeptidyl peptidase IV

Structure activity relationship of N-1 substituted 1,5-naphthyrid-2-one analogs of oxabicyclooctane-linked novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents (Part-9)

Explosible dusts, US codes and standards of safe management practices

A recent explosion protection system failure

Modelling nitrite in wastewater treatment systems: a discussion of different modelling concepts

In Vitro and In Vivo Characterization of the Novel Oxabicyclooctane-Linked Bacterial Topoisomerase Inhibitor AM-8722, a Selective, Potent Inhibitor of Bacterial DNA Gyrase

C1-C2-linker substituted 1,5-naphthyridine analogues of oxabicyclooctane-linked NBTIs as broad-spectrum antibacterial agents (part 7)Electronic supplementary information (ESI) available: Synthetic details of compounds and intermediates. See DOI: 10.1039/c5md00297d

Novel methodologies for the synthesis of C-aryl glycosides and progress toward the synthesis of the C-aryl glycoside natural products galtamycinone and kidamycin

The future of the OSHA PSM standard

ChemInform Abstract: 4-Arylcyclohexylalanine Analogues as Potent, Selective and Orally Active Inhibitors of Dipeptidyl Peptidase IV

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