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Major Structural Components in Freshwater Dissolved Organic Matter

Environmental science & technology, 2007-12, Vol.41 (24), p.8240-8247

2007

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Dereplication of natural products using minimal NMR data inputs

Organic & biomolecular chemistry, 2015-01, Vol.13 (39), p.9957-9962

2015

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Activity-Independent Discovery of Secondary Metabolites Using Chemical Elicitation and Cheminformatic Inference

ACS chemical biology, 2015-11, Vol.10 (11), p.2616-2623

2015

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Structural study of Maya Blue; textural, thermal and solid-state multinuclear magnetic resonance characterization of the palygorskite-indigo and sepiolite-indigo adducts

Clays and clay minerals, 2003-06, Vol.51 (3), p.318-326

2003

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Turning Spiroketals Inside Out: A Rearrangement Triggered by an Enol Ether Epoxidation

ChemistryOpen (Weinheim), 2015-10, Vol.4 (5), p.577-580

2015

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Blind trials of computer-assisted structure elucidation software

Journal of cheminformatics, 2012-02, Vol.4 (1), p.5-5, Article 5

2012

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Assessing the organic composition of urban surface films using nuclear magnetic resonance spectroscopy

Chemosphere (Oxford), 2006-03, Vol.63 (1), p.142-152

2006

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Consolidating and Managing Data for Drug Development within a Pharmaceutical Laboratory: Comparing the Mapping and Reporting Tools from Software Applications

Organic process research & development, 2021-10, Vol.25 (10), p.2177-2187

2021

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Accraspiroketides A‑B, Phenylnaphthacenoid-Derived Polyketides with Unprecedented [6 + 6+6 + 6] + [5 + 5] Spiro-Architecture

Journal of natural products (Washington, D.C.), 2024-04, Vol.87 (4), p.831-836

2024

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Accraspiroketides A-B, Phenylnaphthacenoid-Derived Polyketides with Unprecedented 6 + 6+6 + 6 + 5 + 5 Spiro-Architecture

Journal of natural products (Washington, D.C.), 2024-04, Vol.87 (4), p.831

2024

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Homodimericin A: A Complex Hexacyclic Fungal Metabolite

Journal of the American Chemical Society, 2016-09, Vol.138 (38), p.12324-12327

2016

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The Fundamentals behind solving for unknown Molecular Structures using Computer-Assisted Structure Elucidation: a free software package at the undergraduate and graduate levels

Magnetic resonance in chemistry, 2016-09, Vol.54 (9), p.700-700

2016

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CASE (Computer-Assisted Structure Elucidation) Study for an Undergraduate Organic Chemistry Class

Journal of chemical education, 2020-03, Vol.97 (3), p.855-860

2020

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The fundamentals behind solving for unknown molecular structures using computer-assisted structure elucidation: a free software package at the undergraduate and graduate levels

Magnetic resonance in chemistry, 2016-09, Vol.54 (9), p.701-704

2016

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A CASE (Computer-Assisted Structure Elucidation) for Bench-Top NMR Systems in the Undergraduate Laboratory for De Novo Structure Determination: How Well Can We Do?

Journal of chemical education, 2022-11, Vol.99 (11), p.3780-3788

2022

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Computer-Assisted Structure Elucidation of Black Chokeberry (Aronia melanocarpa) Fruit Juice Isolates with a New Fused Pentacyclic Flavonoid Skeleton

Organic letters, 2015-06, Vol.17 (12), p.2988-2991

2015

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Dereplication of natural products using minimal NMR data inputsElectronic supplementary information (ESI) available: Experimental 1H NMR, 1H-13C HSQC (or HMQC), 1H-1H COSY are provided for the 18 compounds. Full search results. See DOI: 10.1039/C5OB01713K

2015-09

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Characterization and Synthesis of Eudistidine C, a Bioactive Marine Alkaloid with an Intriguing Molecular Scaffold

Journal of organic chemistry, 2016-11, Vol.81 (22), p.10631-10640

2016

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Chlorines Are Not Evenly Substituted in Chlorinated Paraffins: A Predicted NMR Pattern Matching Framework for Isomeric Discrimination in Complex Contaminant Mixtures

Environmental science & technology letters, 2020-07, Vol.7 (7), p.496-503

2020

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Application of a computer‐assisted structure elucidation program for the structural determination of a new terpenoid aldehyde with an unusual skeleton

Magnetic resonance in chemistry, 2017-03, Vol.55 (3), p.210-213

2017

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An Evaluation of Standardized Software for Processing GC/MS Data from Different Vendors' Instruments in a Forensic Laboratory

Journal of forensic sciences, 2013-05, Vol.58 (3), p.764-766

2013

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Structural study of Maya Blue: textural, thermal and solidstate multinuclear magnetic resonance characterization of the palygorskite-indigo and sepiolite-indigo adducts

Clays and clay minerals, 2003-06, Vol.51 (3), p.318-326

2003

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Cover Picture: Turning Spiroketals Inside Out: A Rearrangement Triggered by an Enol Ether Epoxidation (ChemistryOpen 5/2015)

ChemistryOpen (Weinheim), 2015-10, Vol.4 (5), p.541-541

2015

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Turning Spiroketals Inside Out: A Rearrangement Triggered by an Enol Ether Epoxidation

ChemistryOpen (Weinheim), 2015-10, Vol.4 (5), p.542-542

2015

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Quantitative correlation between the pseudo-cavity volume of the p- tert-butylcalix[4]arene tetra-acetamide and the ionic radius of the cationic guests

Polyhedron, 2001-06, Vol.20 (15), p.1897-1901

Moser, Arvin

2001

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Major Structural Components in Freshwater Dissolved Organic Matter

Dereplication of natural products using minimal NMR data inputs

Activity-Independent Discovery of Secondary Metabolites Using Chemical Elicitation and Cheminformatic Inference

Structural study of Maya Blue; textural, thermal and solid-state multinuclear magnetic resonance characterization of the palygorskite-indigo and sepiolite-indigo adducts

Turning Spiroketals Inside Out: A Rearrangement Triggered by an Enol Ether Epoxidation

Blind trials of computer-assisted structure elucidation software

Assessing the organic composition of urban surface films using nuclear magnetic resonance spectroscopy

Consolidating and Managing Data for Drug Development within a Pharmaceutical Laboratory: Comparing the Mapping and Reporting Tools from Software Applications

Accraspiroketides A‑B, Phenylnaphthacenoid-Derived Polyketides with Unprecedented [6 + 6+6 + 6] + [5 + 5] Spiro-Architecture

Accraspiroketides A-B, Phenylnaphthacenoid-Derived Polyketides with Unprecedented 6 + 6+6 + 6 + 5 + 5 Spiro-Architecture

Homodimericin A: A Complex Hexacyclic Fungal Metabolite

The Fundamentals behind solving for unknown Molecular Structures using Computer-Assisted Structure Elucidation: a free software package at the undergraduate and graduate levels

CASE (Computer-Assisted Structure Elucidation) Study for an Undergraduate Organic Chemistry Class

The fundamentals behind solving for unknown molecular structures using computer-assisted structure elucidation: a free software package at the undergraduate and graduate levels

A CASE (Computer-Assisted Structure Elucidation) for Bench-Top NMR Systems in the Undergraduate Laboratory for De Novo Structure Determination: How Well Can We Do?

Computer-Assisted Structure Elucidation of Black Chokeberry (Aronia melanocarpa) Fruit Juice Isolates with a New Fused Pentacyclic Flavonoid Skeleton

Dereplication of natural products using minimal NMR data inputsElectronic supplementary information (ESI) available: Experimental 1H NMR, 1H-13C HSQC (or HMQC), 1H-1H COSY are provided for the 18 compounds. Full search results. See DOI: 10.1039/C5OB01713K

Characterization and Synthesis of Eudistidine C, a Bioactive Marine Alkaloid with an Intriguing Molecular Scaffold

Chlorines Are Not Evenly Substituted in Chlorinated Paraffins: A Predicted NMR Pattern Matching Framework for Isomeric Discrimination in Complex Contaminant Mixtures

Application of a computer‐assisted structure elucidation program for the structural determination of a new terpenoid aldehyde with an unusual skeleton

An Evaluation of Standardized Software for Processing GC/MS Data from Different Vendors' Instruments in a Forensic Laboratory

Structural study of Maya Blue: textural, thermal and solidstate multinuclear magnetic resonance characterization of the palygorskite-indigo and sepiolite-indigo adducts

Cover Picture: Turning Spiroketals Inside Out: A Rearrangement Triggered by an Enol Ether Epoxidation (ChemistryOpen 5/2015)

Turning Spiroketals Inside Out: A Rearrangement Triggered by an Enol Ether Epoxidation

Quantitative correlation between the pseudo-cavity volume of the p- tert-butylcalix[4]arene tetra-acetamide and the ionic radius of the cationic guests

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