Fuh-Rong Tsay | Researchain

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Featured researches published by Fuh-Rong Tsay.

Journal of Organic Chemistry | 2003

An Improved Preparation of 3,5-Bis(trifluoromethyl)acetophenone and Safety Considerations in the Preparation of 3,5-Bis(trifluoromethyl)phenyl Grignard Reagent

Johnnie L. Leazer; Raymond Cvetovich; Fuh-Rong Tsay; Ulf H. Dolling; Thomas P. Vickery; Donald C. Bachert

Journal of Organic Chemistry | 2005

Practical synthesis of the new carbapenem antibiotic ertapenem sodium.

J. Michael Williams; Karel M. J. Brands; Renato T. Skerlj; Ronald B. Jobson; George Marchesini; Karen M. Conrad; Brenda Pipik; Kimberly A. Savary; Fuh-Rong Tsay; Peter G. Houghton; D. Richard Sidler; Ulf-H. Dolling; Lisa DiMichele; Thomas J. Novak

Journal of Organic Chemistry | 1998

PRACTICAL SYNTHESIS OF ANTI-METHICILLIN-RESISTANT STAPHYLOCOCCUS AUREUS (MRSA) CARBAPENEM L-742,728

Nobuyoshi Yasuda; Mark A. Huffman; Guo-Jie Ho; Lyndon C. Xavier; Chunhua Yang; Khateeta M. Emerson; Fuh-Rong Tsay; Yulan Li; Michael H. Kress; Dale L. Rieger; Sandor Karady; Paul Sohar; Newton L. Abramson; Ann E Decamp; David J. Mathre; Alan W. Douglas; Ulf-H. Dolling; Edward J. J. Grabowski; Paul J. Reider

Journal of Organic Chemistry | 2006

Synthesis of a naphthyridone p38 MAP kinase inhibitor.

John Y. L. Chung; Raymond Cvetovich; Mark McLaughlin; Joseph S. Amato; Fuh-Rong Tsay; Mark S. Jensen; Steve Weissman; Daniel Zewge

Journal of Organic Chemistry | 2005

An Efficient Synthesis of a Dual PPAR α/γ Agonist and the Formation of a Sterically Congested α-Aryloxyisobutyric Acid via a Bargellini Reaction

Raymond Cvetovich; John Chung; Michael H. Kress; Joseph S. Amato; Louis Matty; M. David Weingarten; Fuh-Rong Tsay; Zhen Li; George Zhou

Journal of Organic Chemistry | 2002

Development of a New and Practical Route to Chiral 3,4-Disubstituted Cyclopentanones: Asymmetric Alkylation and Intramolecular Cyclopropanation as Key C−C Bond-Forming Steps

Michael Palucki; Joann M. Um; Nobuyoshi Yasuda; David A. Conlon; Fuh-Rong Tsay; Frederick W. Hartner; Yi Hsiao; Benjamin Marcune; Sandor Karady; David L. Hughes; Peter G. Dormer; Paul J. Reider

Journal of Organic Chemistry | 2005

Stereoselective syntheses of highly functionalized bicyclo[3.1.0]hexanes: a general methodology for the synthesis of potent and selective mGluR2/3 agonists.

Lushi Tan; Nobuyoshi Yasuda; Naoki Yoshikawa; Frederick W. Hartner; Kan Kaung Eng; William R. Leonard; Fuh-Rong Tsay; Ralph P. Volante; Richard D. Tillyer

Journal of Organic Chemistry | 2003

Synthesis of 3-Aminopyrazinone Mediated by 2-Pyridylthioimidate−ZnCl2 Complexes. Development of an Efficient Route to a Thrombin Inhibitor

John Chung; Raymond Cvetovich; Fuh-Rong Tsay; Peter G. Dormer; Lisa DiMichele; David J. Mathre; Jennifer R. Chilenski; and Bing Mao; Robert M. Wenslow

Journal of Organic Chemistry | 1996

A Highly Efficient Synthesis of Fibrinogen Receptor Antagonist L-734,217 via a Novel Chemoselective Silyl-Mediated Conjugate Addition of δ-Lactams to 4-Vinylpyridine

John Y. L. Chung; David L. Hughes; Dalian Zhao; Zhiguo Song; David J. Mathre; Guo-Jie Ho; James M. McNamara; Alan W. Douglas; Robert A. Reamer; Fuh-Rong Tsay; Richard J. Varsolona; James A Mccauley; and Edward J. J. Grabowski; Paul J. Reider

Organic Process Research & Development | 2006

Understanding the Origin of Unusual Stepwise Hydrogenation Kinetics in the Synthesis of the 3-(4-Fluorophenyl)morpholine Moiety of NK1 Receptor Antagonist Aprepitant

Karel M. J. Brands; Shane W. Krska; Thorsten Rosner; Karen M. Conrad; Edward G. Corley; Mahmoud Kaba; Robert D. Larsen; Robert A. Reamer; and Yongkui Sun; Fuh-Rong Tsay

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