E. Voight

发表

Desymmetrization of pibrentasvir for efficient prodrug synthesis†

J. Randolph, Jan E. Waters, E. Voight, 2021, Chemical science.

TRPV1 ligands with hyperthermic, hypothermic and no temperature effects in rats

A. Gomtsyan, J. Segreti, Robert G. Schmidt, 2015, Temperature.

Formal synthesis of (−)-N-acetylneuraminic acid (Neu5Ac) via desymmetrization by ring-closing metathesis

C. Rein, E. Voight, S. D. Burke, 2001 .

Formal synthesis of (+)-3-deoxy-D-glycero-D-galacto-2-nonulosonic acid (KDN) via desymmetrization by ring-closing metathesis.

E. Voight, S. D. Burke, 2001, Organic letters.

Synthesis of sialic acids via desymmetrization by ring-closing metathesis.

C. Rein, E. Voight, S. D. Burke, 2002, The Journal of organic chemistry.

Structure−Activity Relationship Studies on a Series of Novel, Substituted 1-Benzyl-5-phenyltetrazole P2X7 Antagonists

D. Donnelly-roberts, P. Honore, M. Jarvis, 2006 .

On-DNA Hydroalkylation to Introduce Diverse Bicyclo[1.1.1]pentanes and Abundant Alkyls via Halogen Atom Transfer.

Jadab Majhi, G. Molander, E. A. Crane, 2022, Journal of the American Chemical Society.

Synthesis of Substituted Cyclopropanecarboxylates via Room Temperature Palladium-Catalyzed α-Arylation of Reformatsky Reagents.

E. Voight, Stephen N. Greszler, Geoff T. Halvorsen, 2017, Organic letters.

Regio- and Stereoselective Rhodium(II)-Catalyzed C-H Functionalization of Cyclobutanes.

Wenbin Liu, H. Davies, Zachary J. Garlets, 2020, Chem.

Synthesis of the bryostatin 1 northern hemisphere (C1-C16) via desymmetrization by ketalization/ring-closing metathesis.

H. Seradj, E. Voight, S. D. Burke, 2004, Organic letters.

Regio- and Stereoselective Rhodium(II)-Catalyzed C-H Functionalization of Organosilanes by Donor/Acceptor Carbenes Derived from Aryldiazoacetates.

H. Davies, Zachary J. Garlets, Jiantao Fu, 2019, Organic letters.

Target-directed synthesis of antibacterial drug candidate GSK966587.

Ilaria Giordano, A. Hennessy, J. L. Wood, 2010, Organic letters.

Discovery of (R)-1-(7-chloro-2,2-bis(fluoromethyl)chroman-4-yl)-3-(3-methylisoquinolin-5-yl)urea (A-1165442): a temperature-neutral transient receptor potential vanilloid-1 (TRPV1) antagonist with analgesic efficacy.

A. Gomtsyan, J. Segreti, A. King, 2014, Journal of medicinal chemistry.

Pharmacology of Modality-Specific Transient Receptor Potential Vanilloid-1 Antagonists That Do Not Alter Body Temperature

A. Gomtsyan, P. Mantyh, J. Segreti, 2012, Journal of Pharmacology and Experimental Therapeutics.

Synthesis of (+)-didemniserinolipid B: application of a 2-allyl-4-fluorophenyl auxiliary for relay ring-closing metathesis.

J. Suh, C. C. Marvin, E. Voight, 2008, The Journal of organic chemistry.

Synthesis of (+)-didemniserinolipid B via ketalization/ring-closing metathesis.

C. C. Marvin, E. Voight, S. D. Burke, 2007, Organic letters.

Stereoselective Synthesis of a Dipyridyl Transient Receptor Potential Vanilloid-3 (TRPV3) Antagonist.

A. Gomtsyan, Robert G. Schmidt, P. Kym, 2016, The Journal of organic chemistry.

Lithioarene Cycliacylation and Pd-Catalyzed Aminoethylation/Cyclization to Access Electronically Diverse Saturated Isoquinoline Derivatives.

Elliot P Farney, G. Gfesser, E. Voight, 2021, The Journal of organic chemistry.

Synthesis and Pharmacology of (Pyridin-2-yl)methanol Derivatives as Novel and Selective Transient Receptor Potential Vanilloid 3 Antagonists.

Bruce Clapham, Bin Li, A. Gomtsyan, 2016, Journal of medicinal chemistry.

Stereochemically general approach to adjacent bis(tetrahydrofuran) cores of annonaceous acetogenins.

E. Voight, S. D. Burke, L. Wysocki, 2006, Organic letters.

Desymmetrization of pibrentasvir for efficient prodrug synthesis†

J. Randolph, Jan E. Waters, E. Voight, 2021, Chemical science.

General Asymmetric Synthesis of Densely Functionalized Pyrrolidines via Endo-Selective [3+2] Cycloaddition of β-Quaternary-Substituted Nitroalkenes and Azomethine Ylides.

E. Voight, Stephen N. Greszler, Gang Zhao, 2020, The Journal of organic chemistry.

Synthesis of A-9758, an Inverse Agonist of Retinoic Acid-Related Orphan Receptor γt

C. C. Marvin, E. Voight, Stephen N. Greszler, 2022, ACS omega.

Fueling the Pipeline via Innovations in Organic Synthesis.

P. Kym, E. Voight, Stephen N. Greszler, 2021, ACS medicinal chemistry letters.

Pharmacology of Modality-Specific TRPV1 Antagonists That Do Not Alter Body Temperature

A. Gomtsyan, P. Mantyh, J. Segreti, 2012 .

Continuous Process to Safely Manufacture an Aryldiazoacetate and Its Direct Use in a Dirhodium-Catalyzed Enantioselective Cyclopropanation

Onkar N. Manjrekar, Eric R. Sacia, Laurie B. Mlinar, 2022, Organic Process Research & Development.

Synthesis of ABBV-168, a 2'-Bromouridine for the Treatment of Hepatitis C.

Michael T. Tudesco, Eric G. Moschetta, N. Ide, 2018, The Journal of organic chemistry.

Asymmetric synthesis of pharmaceutically relevant 1-aryl-2-heteroaryl- and 1,2-diheteroarylcyclopropane-1-carboxylates

W. Gong, H. Davies, E. Voight, 2021, Chemical science.

Prodrug Strategies to Improve the Solubility of HCV NS5A Inhibitor Pibrentasvir (ABT-530).

Brice E. Uno, J. Randolph, Deanne F. Stolarik, 2020, Journal of medicinal chemistry.

Synthesis of 2,2,2,-Trichloroethyl Aryl- and Vinyldiazoacetates by Palladium-Catalyzed Cross-Coupling.

H. Davies, L. Fu, E. Voight, 2017, Chemistry.

Foslevodopa/Foscarbidopa: A New Subcutaneous Treatment for Parkinson's Disease

M. Facheris, Geoff G. Z. Zhang, F. Jameel, 2021, Annals of neurology.

Scalable Asymmetric Syntheses of Foslevodopa and Foscarbidopa Drug Substances for the Treatment of Parkinson's Disease.

Brian J. Kotecki, A. Ashok, D. Hill, 2021, The Journal of organic chemistry.

Synthesis and evaluation of 2'-dihalo ribonucleotide prodrugs with activity against hepatitis C virus.

J. Randolph, R. Henry, Hui-ju Chen, 2019, Bioorganic & medicinal chemistry.

Enabling Synthesis of ABBV-2222, A CFTR Corrector for the Treatment of Cystic Fibrosis.

E. Voight, Stephen N. Greszler, Bhadra H. Shelat, 2019, Organic letters.

Transient receptor potential vanilloid-1 antagonists: a survey of recent patent literature

M. Kort, E. Voight, 2010, Expert opinion on therapeutic patents.

Efficient preparation of chiral diamines via Red-Al reduction of N-Boc-protected amino acid-derived secondary amides

E. Voight, M. H. Kress, N. Ikemoto, 2006 .

Enabling Asymmetric Synthesis of ABBV-3748, a Corrector Compound for the Treatment of Cystic Fibrosis.

E. Voight, Stephen N. Greszler, Bhadra H. Shelat, 2022, Organic letters.

Efficient Preparation of Chiral Diamines via Red‐Al Reduction of N‐Boc‐Protected Amino Acid‐Derived Secondary Amides.

E. Voight, M. H. Kress, N. Ikemoto, 2006 .

Synthesis of Substituted Cyclopropanecarboxylates via Room Temperature Palladium-Catalyzed α-Arylation of Reformatsky Reagents.

E. Voight, Stephen N. Greszler, Geoff T. Halvorsen, 2017, Organic Letters.

Synthesis and Pharmacology of (Pyridin-2-yl)methanol Derivatives as Novel and Selective Transient Receptor Potential Vanilloid 3 Antagonists.

A. Gomtsyan, J. Segreti, R. Henry, 2016, Journal of medicinal chemistry.