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Fluorodecarboxylation for the Synthesis of Trifluoromethyl Aryl Ethers.
Published in:
Angewandte Chemie, 2016, v. 128, n. 33, p. 9910, doi. 10.1002/ange.201604793
By:
- Zhang, Qing ‐ Wei;
- Brusoe, Andrew T.;
- Mascitti, Vincent;
- Hesp, Kevin D.;
- Blakemore, David C.;
- Kohrt, Jeffrey T.;
- Hartwig, John F.
Publication type:
Article
Fluorodecarboxylation for the Synthesis of Trifluoromethyl Aryl Ethers.
Published in:
Angewandte Chemie International Edition, 2016, v. 55, n. 33, p. 9758, doi. 10.1002/anie.201604793
By:
- Zhang, Qing‐Wei;
- Brusoe, Andrew T.;
- Mascitti, Vincent;
- Hesp, Kevin D.;
- Blakemore, David C.;
- Kohrt, Jeffrey T.;
- Hartwig, John F.
Publication type:
Article
The Discovery of (2 R,4 R)- N-(4-chlorophenyl)- N- (2-fluoro-4-(2-oxopyridin-1(2 H)-yl)phenyl)-4-methoxypyrrolidine-1,2-dicarboxamide (PD 0348292), an Orally Efficacious Factor Xa Inhibitor.
Published in:
Chemical Biology & Drug Design, 2007, v. 70, n. 2, p. 100, doi. 10.1111/j.1747-0285.2007.00539.x
By:
- Kohrt, Jeffrey T.;
- Bigge, Christopher F.;
- Bryant, John W.;
- Casimiro-Garcia, Agustin;
- Chi, Liguo;
- Cody, Wayne L.;
- Dahring, Tawny;
- Dudley, Danette A.;
- Filipski, Kevin J.;
- Haarer, Staci;
- Heemstra, Ron;
- Janiczek, Nancy;
- Narasimhan, Lakshmi;
- McClanahan, Thomas;
- Peterson, J. Thomas;
- Sahasrabudhe, Vaisheli;
- Schaum, Robert;
- Van Huis, Chad A.;
- Welch, Kathleen M.;
- Zhang, Erli
Publication type:
Article
Structure-based Drug Design of Pyrrolidine-1, 2-dicarboxamides as a Novel Series of Orally Bioavailable Factor Xa Inhibitors.
Published in:
2007
By:
- Van Huis, Chad A.;
- Bigge, Christopher F.;
- Casimiro-Garcia, Agustin;
- Cody, Wayne L.;
- Dudley, Danette A.;
- Filipski, Kevin J.;
- Heemstra, Ronald J.;
- Kohrt, Jeffrey T.;
- Narasimhan, Lakshmi S.;
- Schaum, Robert P.;
- Zhang, Erli;
- Bryant, John W.;
- Haarer, Staci;
- Janiczek, Nancy;
- Leadley, Robert J.;
- McClanahan, Thomas;
- Peterson, J. Thomas;
- Welch, Kathleen M.;
- Edmunds, Jeremy J.
Publication type:
Letter
Cell‐free in vitro reduction of carboxylates to aldehydes: With crude enzyme preparations to a key pharmaceutical building block.
Published in:
Biotechnology Journal, 2021, v. 16, n. 4, p. 1, doi. 10.1002/biot.202000315
By:
- Schwarz, Anna;
- Hecko, Sebastian;
- Rudroff, Florian;
- Kohrt, Jeffrey T.;
- Howard, Roger M.;
- Winkler, Margit
Publication type:
Article
FUSED PYRAZOLE SYNTHESIS BY N-N BOND FORMATION: THE PYRAZOLO [5,1-b] BENZOTHIAZOLE SYSTEM.
Published in:
Heterocyclic Communications, 1997, v. 3, n. 3, p. 201
By:
- Bates, Dallas K.;
- Kohrt, Jeffrey T.;
- Folk, Heather;
- Mingde Xia
Publication type:
Article

Found: 6

Fluorodecarboxylation for the Synthesis of Trifluoromethyl Aryl Ethers.

Fluorodecarboxylation for the Synthesis of Trifluoromethyl Aryl Ethers.

The Discovery of (2 R,4 R)- N-(4-chlorophenyl)- N- (2-fluoro-4-(2-oxopyridin-1(2 H)-yl)phenyl)-4-methoxypyrrolidine-1,2-dicarboxamide (PD 0348292), an Orally Efficacious Factor Xa Inhibitor.

Structure-based Drug Design of Pyrrolidine-1, 2-dicarboxamides as a Novel Series of Orally Bioavailable Factor Xa Inhibitors.

Cell‐free in vitro reduction of carboxylates to aldehydes: With crude enzyme preparations to a key pharmaceutical building block.

FUSED PYRAZOLE SYNTHESIS BY N-N BOND FORMATION: THE PYRAZOLO [5,1-b] BENZOTHIAZOLE SYSTEM.