126063-08-9Relevant articles and documents
A Simple and Economical Synthetic Route to p-Ethynylaniline and Ethynyl-Terminated Substrates
Melissaris, Anastasios P.,Litt, Morton H.
, p. 5818 - 5821 (1994)
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Switching reaction pathways of trifluoromethylated thiobenzanilides by choice of different oxidative systems
Zhu, Jiangtao,Xie, Haibo,Li, Shan,Chen, Zixian,Wu, Yongming
, p. 306 - 309 (2011/06/20)
Trifluoromethylated thiobenzanilides are efficiently converted to 2-trifluoromethylbenzothiazoles via intramolecular oxidative cyclization under CAN/NaHCO3 oxidation, while the dimerized products with "-S-S-" bond linkage are obtained when PIDA
Sulfonylaminovalerolactams and derivatives thereof as factor Xa inhibitors
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Page/Page column 48, (2008/06/13)
The present application describes sulfonylaminovalerolactams and derivatives thereof of Formula I: or pharmaceutically acceptable salt forms thereof, wherein ring G is a mono- or bicyclic carbocycle or heterocycle. Compounds of the present invention are useful as inhibitors of trypsin-like serine proteases, specifically factor Xa.