Andrew F Nolting

发表

Synthesis of vaniprevir (MK-7009): lactamization to prepare a 20-membered [corrected] macrocycle.

Paul N. Devine, D. Tellers, D. Zewge, 2011, The Journal of organic chemistry.

New reactions and processes for the efficient synthesis of a HCV NS5b prodrug

Rebecca T. Ruck, Jon A. Jurica, E. Sirota, 2018 .

Practical Synthesis of A Macrocyclic HCV Protease Inhibitor: A High-Yielding Macrolactam Formation

Paul N. Devine, D. Tellers, D. Zewge, 2014 .

Discovery of MK-8831, A Novel Spiro-Proline Macrocycle as a Pan-Genotypic HCV-NS3/4a Protease Inhibitor.

Charles L. Jayne, Rebecca T. Ruck, Yongxin Han, 2016, ACS medicinal chemistry letters.

Development of ProTx-II Analogues as Highly Selective Peptide Blockers of Nav1.7 for the Treatment of Pain.

D. Henze, S. Grauer, A. Palani, 2021, Journal of medicinal chemistry.

Synthesis of the C6-C21 segment of amphidinolide E.

J. A. Marshall, Andrew F Nolting, G. Schaaf, 2005, Organic letters.

Asymmetric Synthesis of Tertiary and Secondary Cyclopropyl Boronates via Cyclopropanation of Enantioenriched Alkenyl Boronic Esters.

M. Emmert, Serge Ruccolo, Andrew F Nolting, 2022, Organic letters.

Discovery of 2-Pyridinone Aminals: A Prodrug Strategy to Advance a Second Generation of HIV-1 Integrase Strand Transfer Inhibitors.

John D. Schreier, Min Xu, D. Hazuda, 2015, Journal of medicinal chemistry.

Structure-Activity Relationship of Novel and Selective Biaryl-Chroman GPR40 AgoPAMs.

A. Howard, D. Tatosian, R. Orr, 2018, ACS medicinal chemistry letters.

Design and Synthesis of Novel, Selective GPR40 AgoPAMs.

A. Howard, R. Nargund, W. Hagmann, 2017, ACS medicinal chemistry letters.

Development of a novel class of potent and selective FIXa inhibitors.

E. Sherer, K. Ellsworth, W. Geissler, 2015, Bioorganic & medicinal chemistry letters.

Enantioselective Synthesis of α-Methyl-β-cyclopropyldihydrocinnamates.

Rebecca T. Ruck, R. Orr, Louis-Charles Campeau, 2016, The Journal of organic chemistry.

Correction to Discovery of 2-Pyridinone Aminals: A Prodrug Strategy to Advance a Second Generation of HIV-1 Integrase Strand Transfer Inhibitors.

John D. Schreier, Min Xu, D. Hazuda, 2016, Journal of Medicinal Chemistry.

Design and Synthesis of Novel, Selective GPR40 AgoPAMs.

A. Howard, R. Nargund, W. Hagmann, 2017, ACS Medicinal Chemistry Letters.

A Modular Synthesis of 2-Alkyl- and 2-Arylchromans via a Three-Step Sequence

Rebecca T. Ruck, B. Pio, R. Orr, 2016, Synthesis.