82595-41-3Relevant academic research and scientific papers
An odorless, one-pot synthesis of nitroaryl thioethers via SNAr reactions through the in situ generation of S-alkylisothiouronium salts
Lu, Guo-Ping,Cai, Chun
, p. 59990 - 59996 (2015/02/19)
A newly developed C-S bond formation nucleophilic aromatic substitution (SNAr) reaction in aqueous Triton X-100 (TX100) micelles has been disclosed. This chemistry, in which odorless, cheap and stable thiourea in place of thiols is used as the sulfur reagent, provides an efficient approach for the generation of nitroaryl thioethers, which are useful structural units of many bioactive molecules, rendering this methodology attractive to both synthetic and medicinal chemistry.
BENZOXAZINES, BENZOTHIAZINES, AND RELATED COMPOUNDS HAVING NOS INHIBITORY ACTIVITY
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Page/Page column 68-69, (2010/02/17)
The present invention features benzoxazines, benzothiazines, and related compounds that inhibit nitric oxide synthase (NOS), particularly those that selectively inhibit neuronal nitric oxide synthase (nNOS) in preference to other NOS isoforms. The NOS inh
Synthesis and structure of a thioazobenzene palladacycle: oxygen insertion into the Pd-C bond by m-chloroperbenzoic acid
Pal, Chandan Kumar,Chattopadhyay, Surajit,Sinha, Chittaranjan,Chakravorty, Animesh
, p. 91 - 99 (2007/10/02)
The reaction of p-tolyl-o'-(2-chloroethylthio)azobenzene (LIH) with Na2PdCl4 affords the complex PdLICl, the structure of which has been determined by X-ray crystallography.The azobenzene ligand acts in the tridentate (C,N,S) fashion
Synthesis and Reactivity of 4-Substituted-2,3-dihydrobenzo-1,4-thiazines
Florio, Saverio,Leng, John L.,Stirling, Charles J. M.
, p. 237 - 240 (2007/10/02)
A series of derivatives of 4H-2,3-dihydrobenzo-1,4-thiazine has been prepared. 4-Acetyl-2,3-dihydrobenzo-1,4-thiazine undergoes self-condensation by n-butylmagnesium bromide affording the corresponding 4-acetoacetyl-2,3-dihydrobenzo-1,4-thiazine, which, i
