Search Results - "Wittenberger, Steven J."
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A Laser Driven Flow Chemistry Platform for Scaling Photochemical Reactions with Visible Light
Published in ACS central science (23-01-2019)“…Visible-light-promoted organic reactions can offer increased reactivity and selectivity via unique reaction pathways to address a multitude of practical…”
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The Enabling Technologies Consortium (ETC): Fostering Precompetitive Collaborations on New Enabling Technologies for Pharmaceutical Research and Development
Published in Organic process research & development (17-03-2017)“…The creation of the Enabling Technologies Consortium (ETC) is described. The ETC fosters precompetitive collaborations aimed at the development and evaluation…”
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Development of a Catalytic Enantioselective Conjugate Addition of 1,3-Dicarbonyl Compounds to Nitroalkenes for the Synthesis of Endothelin-A Antagonist ABT-546. Scope, Mechanism, and Further Application to the Synthesis of the Antidepressant Rolipram
Published in Journal of the American Chemical Society (06-11-2002)“…The enantioselective synthesis of endothelin-A antagonist ABT-546 has been accomplished via the discovery and development of a highly selective catalytic…”
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Catalytic Enantioselective Conjugate Addition of 1,3-Dicarbonyl Compounds to Nitroalkenes
Published in Journal of the American Chemical Society (03-11-1999)Get full text
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5
Addition of Organometallic Reagents to N-Glycosyl Nitrones. Enantioselective Syntheses of (+)-(R)- and (-)-(S)-Zileuton
Published in Journal of organic chemistry (01-10-1994)Get full text
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2,2,2-Trifluoroethyl Formate: A Versatile and Selective Reagent for the Formylation of Alcohols, Amines, and N-Hydroxylamines
Published in Organic letters (10-01-2002)“…Treatment of a variety of alcohols, amines, and N-hydroxylamines with 2,2,2-trifluoroethyl formate gave the corresponding formylated adducts in high yields…”
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7
The Development of a Large-Scale Synthesis of Matrix Metalloproteinase Inhibitor, ABT-518
Published in Organic process research & development (01-05-2002)“…A process for the preparation of matrix metalloproteinase inhibitor ABT-518 has been developed. Significant improvements have been made to the first generation…”
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Development of a Scalable Synthesis of Dipeptidyl Peptidase-4 Inhibitor ABT-279
Published in Organic process research & development (20-11-2009)“…A convergent, scalable synthesis of dipeptidyl peptidase-4 inhibitor, ABT-279, has been developed and demonstrated on multikilogram scale. The…”
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A highly diastereoselective vinylogous Mannich condensation and 1,4-conjugate addition of ( Z)-propenyl cuprate in the synthesis of an influenza neuraminidase inhibitor
Published in Tetrahedron: asymmetry (01-11-2003)“…A practical synthesis of neuraminidase influenza inhibitor, A-322278, has been developed. Asymmetry is introduced into the synthesis by an enzyme mediated…”
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Impurity rejection in the crystallization of ABT-510 as a method to establish starting material specifications
Published in Advances in experimental medicine and biology (2009)“…Understanding impurity rejection in a drug substance crystallization process is valuable for establishing purity specifications for the starting materials used…”
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Dialkyltin oxide mediated addition of trimethylsilyl azide to nitriles. A novel preparation of 5-substituted tetrazols
Published in Journal of organic chemistry (01-07-1993)Get full text
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12
A Scaleable Synthesis of Fiduxosin
Published in Organic process research & development (01-11-2004)“…Fiduxosin (1) has been under development at Abbott Laboratories for the treatment of benign prostatic hyperplasia. A convergent strategy required methodologies…”
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An Improved Synthesis of Pyran-3,5-dione: Application to the Synthesis of ABT-598, a Potassium Channel Opener, via Hantzsch Reaction
Published in Journal of organic chemistry (17-02-2006)“…Ketoester 1 is cyclized to give pyran-3,5-dione 2 in 78% yield using a parallel addition of ketoester 1 and base NaO t Bu in refluxing THF. Compared to the…”
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An Efficient Synthesis of the Cholinergic Channel Activator ABT-418
Published in Journal of organic chemistry (12-01-1996)Get full text
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15
Synthesis of an Influenza Neuraminidase Inhibitor Intermediate via a Highly Diastereoselective Coupling Reaction
Published in Organic letters (02-05-2002)“…A highly diastereoselective coupling reaction between TBSOP (3) and trityl sulfenimine 4 was developed which provided influenza neuraminidase inhibitor…”
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An Efficient Scalable Process for the Synthesis of N-Boc-2-tert-butyldimethylsiloxypyrrole
Published in Organic process research & development (01-07-2002)“…A safe, reliable and scalable process for the preparation of N-Boc-2-tert-butyldimethylsiloxy-pyrrole (TBSOP) is described. In a three-step, one-pot sequence…”
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Heuristics, Protocol, and Considerations for Flow Chemistry in Photoredox Catalysis
Published in ChemPhotoChem (01-12-2017)“…Heuristics for employing photoredox catalysts in coiled‐tube LED reactors for flow chemistry are presented. These heuristics focus on common reaction…”
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A general synthesis of N-aryl- and N-alkyl-2-aminobenzoxazoles
Published in Tetrahedron letters (28-11-2005)“…An efficient and practical synthetic procedure is described for the preparation of a variety of N-substituted aryl- and alkyl-2-aminobenzoxazoles. This new…”
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Dialkyltin oxide mediated addition of trimethylsilyl azide to nitriles. A novel preparation of 5-substituted tetrazoles
Published in Journal of organic chemistry (16-07-1993)Get full text
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The synthesis of ketolide antibiotic ABT-773 (cethromycin)
Published in Tetrahedron (01-11-2004)“…A practical and efficient synthesis of ketolide antibiotic cethromycin (ABT-773) ( 1 ) is described. An effective protection strategy allows high yielding,…”
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