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Jeremy P. Scott

Observed names: J. P. SCOTT, J. P. Scott, J. Scott, Jeremy Scott, Scott, J. P., Scott, Jeremy P.
Observed institutions: University of Lethbridge, Merck & Co., Inc., Rahway, NJ, USA (United States), University of Arizona, University of St Andrews, University of California, Irvine, University of Cambridge, MSD (UK) Limited (United Kingdom), Pharmaron (United Kingdom)
ORCID: 0009-0000-3882-9242
Observed ORCID: 0009-0000-3882-9242
OpenAlex ID: A5073242530
Toxicological Assessment of 2-Methyltetrahydrofuran and Cyclopentyl Methyl Ether in Support of Their Use in Pharmaceutical Chemical Process Development
2011 · Vincent Antonucci, John Coleman, et al. · Organic Process Research & Development · 211
A Practical Synthesis of (+)-Discodermolide and Analogues: Fragment Union by Complex Aldol Reactions
2001 · Ian Paterson, Gordon J. Florence, et al. · Journal of the American Chemical Society · 208
Total Synthesis of the Antimicrotubule Agent (+)-Discodermolide Using Boron-Mediated Aldol Reactions of Chiral Ketones
2000 · Ian Paterson, Gordon J. Florence, et al. · Angewandte Chemie International Edition · 133
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Catalytic, Asymmetric, and Stereodivergent Synthesis of Non-Symmetric β,β-Diaryl-α-Amino Acids
2014 · Carmela Molinaro, Jeremy P. Scott, et al. · Journal of the American Chemical Society · 107
Total Synthesis of (±)-Didehydrostemofoline (Asparagamine A) and (±)-Isodidehydrostemofoline
2003 · Markus Brüggemann, Andrew I. McDonald, et al. · Journal of the American Chemical Society · 101
1,6-Asymmetric Induction in Boron-Mediated Aldol Reactions: Application to a Practical Total Synthesis of (+)-Discodermolide
2002 · Ian Paterson, Oscar Delgado, et al. · Organic Letters · 77
A Second-Generation Total Synthesis of (+)-Discodermolide: The Development of a Practical Route Using Solely Substrate-Based Stereocontrol
2004 · Ian Paterson, Oscar Delgado, et al. · The Journal of Organic Chemistry · 72
A Green Chemistry Continuum for a Robust and Sustainable Active Pharmaceutical Ingredient Supply Chain
2019 · Stefan G. Koenig, Cisco Bee, et al. · ACS Sustainable Chemistry & Engineering · 61
Evolution of a Manufacturing Route to Omarigliptin, A Long-Acting DPP-4 Inhibitor for the Treatment of Type 2 Diabetes
2015 · John Y. L. Chung, Jeremy P. Scott, et al. · Organic Process Research & Development · 59
Practical Asymmetric Synthesis of a γ-Secretase Inhibitor Exploiting Substrate-Controlled Intramolecular Nitrile Oxide−Olefin Cycloaddition
2006 · Jeremy P. Scott, Steven F. Oliver, et al. · The Journal of Organic Chemistry · 53
Mitsunobu Inversion of a Secondary Alcohol with Diphenylphosphoryl azide. Application to the Enantioselective Multikilogram Synthesis of a HCV Polymerase Inhibitor
2011 · Jeremy P. Scott, Mahbub Alam, et al. · Organic Process Research & Development · 42
Total Synthesis of the Antimicrotubule Agent (+)-Discodermolide Using Boron-Mediated Aldol Reactions of Chiral Ketones
2000 · Ian Paterson, Gordon J. Florence, et al. · Angewandte Chemie · 40
Asymmetric Synthesis of a Glucagon Receptor Antagonist via Friedel–Crafts Alkylation of Indole with Chiral α-Phenyl Benzyl Cation
2012 · John Y. L. Chung, Dietrich Steinhuebel, et al. · Organic Process Research & Development · 38
Development of a Phase Transfer Catalyzed Asymmetric Synthesis for an Estrogen Receptor Beta Selective Agonist
2007 · Jeremy P. Scott, Michael S. Ashwood, et al. · Organic Process Research & Development · 38
Asymmetric Synthesis of Highly Functionalized Tetrahydropyran DPP-4 Inhibitor
2014 · Feng Xu, Michael J. Zacuto, et al. · Organic Letters · 36
Laboratory emulation of polyketide biosynthesis: an iterative, aldol-based, synthetic entry to polyketide libraries using (R)- and (S )-1-(benzyloxy)-2-methylpentan-3-one, and conformational aspects of extended polypropionates
1999 · Ian Paterson, Jeremy P. Scott · Journal of the Chemical Society Perkin Transactions 1 · 35
A Practical Synthesis of a γ-Secretase Inhibitor
2007 · Jeremy P. Scott, David R. Lieberman, et al. · The Journal of Organic Chemistry · 34
Process Development and Large-Scale Synthesis of a c-Met Kinase Inhibitor
2010 · Gavin W. Stewart, Karel M. J. Brands, et al. · Organic Process Research & Development · 28
Enantioselective Synthesis of β-Aryloxycarboxylic Esters via Asymmetric Hydrogenation of β-Aryloxy-α,β-Unsaturated Esters
2012 · Gavin W. Stewart, Michael Shevlin, et al. · Organic Letters · 26
Polyketide library synthesis: Conformational control in extended polypropionates
1997 · Ian Paterson, Jeremy P. Scott · Tetrahedron Letters · 24
Synthesis of Bis-Macrocyclic HCV Protease Inhibitor MK-6325 via Intramolecular sp2–sp3 Suzuki–Miyaura Coupling and Ring Closing Metathesis
2015 · Hongmei Li, Jeremy P. Scott, et al. · Organic Letters · 23
Polyketide library synthesis: Iterative assembly of extended polypropionates using (R)- and (S)-1-(benzyloxy)-2-methylpentan-3-one
1997 · Ian Paterson, Jeremy P. Scott · Tetrahedron Letters · 21
An approach to heterodiarylmethanes via sp2–sp3 Suzuki−Miyaura cross-coupling
2016 · Gavin W. Stewart, Peter E. Maligres, et al. · Tetrahedron · 20
Process Development of the HCV NS5B Site D Inhibitor MK-8876
2016 · Michael J. Williams, Qinghao Chen, et al. · Organic Process Research & Development · 18
Enantioselective Synthesis of a Highly Substituted Tetrahydrofluorene Derivative as a Potent and Selective Estrogen Receptor Beta Agonist
2014 · Matthew L. Maddess, Jeremy P. Scott, et al. · Organic Process Research & Development · 17
Works count: 59
Citation count: 1,662
H-index: 21
I10-index: 34
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