134306-34-6Relevant academic research and scientific papers
The effect of substituents on the chiral solvating properties of (S)-1,6-dialkylpiperazine-2,5-diones
Malavasic, Crt,Stanovnik, Branko,Wagger, Jernej,Svete, Jurij
experimental part, p. 1364 - 1371 (2011/11/29)
The effect of substituents on the chiral solvating properties of 13 different (S)-1,6-dialkylpiperazine-2,5-diones (S)-1a-m and five (3S,6S)-1,3,6-trialkyl analogues (S,S)-1n-r was studied by NMR in CDCl 3 with methyl (RS)-N-benzoylleucinate (R
Synthesis and SAR Studies of diarylpyrrole anticoccidial agents
Qian, Xiaoxia,Liang, Gui-Bai,Feng, Dennis,Fisher, Michael,Crumley, Tami,Rattray, Sandra,Dulski, Paula M.,Gurnett, Anne,Leavitt, Penny Sue,Liberator, Paul A.,Misura, Andrew S.,Samaras, Samantha,Tamas, Tamas,Schmatz, Dennis M.,Wyvratt, Matthew,Biftu, Tesfaye
, p. 2817 - 2821 (2007/10/03)
2-(4-Fluorophenyl)-3-(4-pyridinyl)-5-substituted pyrroles were prepared and evaluated as anticoccidial agents in both in vitro and in vivo assays. Among the compounds evaluated, the dimethylamine-substituted pyrrole 19a is the most potent inhibitor of Eimeria tenella PKG (cGMP-dependent protein kinase). Further SAR studies on the side chain of the 2-pyrrolidine nitrogen did not enhance in vivo anticoccidial activity.
Stereoselective synthesis of allylic amines by rearrangement of allylic trifluoroacetimidates: Stereoselective synthesis of polyoxamic acid and derivatives of other α-amino acids
Savage, Ian,Thomas, Eric J.,Wilson, Peter D.
, p. 3291 - 3303 (2007/10/03)
On heating in xylene under reflux, allylic trifluoroacetimidates undergo [3,3] sigmatropic rearrangement to regioisomeric allylic trifluoroacetamides. Examples include the rearrangements of the trifluoroacetimidates 16 and 73 to the trifluoroacetamides 17 and 74, which were incorporated into stereoselective syntheses of polyoxamic acid 1, and the rearrangement of the trifluoroacetimidate 26. The rearrangement was the key step in asymmetric syntheses of the (S)- and (R)-valine derivatives 37 and 48. Other examples include rearrangements of the trifluoroacetimidates 52, 54 and 56 prepared from geraniol, cinnamyl alcohol and sorbyl alcohol, respectively, and the more complex trifluoroacetimidates 62 and 69. The stereoselectivity of these rearrangements, which are somewhat faster than rearrangements of analogous allylic trichloroacetimidates, is consistent with the participation of chair-like, six-membered, transition structures. The Royal Society of Chemistry 1999.
Tertiary-butyldimethylsilyl carbamate derivative and process for producing the same
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, (2008/06/13)
A t-butyldimethylsilyl carbamate derivative and a process for producing the same are disclosed. Tertiary-butyldimethylsilyl carbamate derivatives having the following general formula (1) are intermediates for the production of a variety of carbamate ester
A Synthesis of a New Type of Alkoxycarbonylating Reagents from 1,1-Bis Carbonate (BTBC) and Their Reactions
Takeda, Kazuyoshi,Tsuboyama, Kanoko,Hoshino, Mitsuho,Kishino, Miyuki,Ogura, Haruo
, p. 557 - 560 (2007/10/02)
1,1'-Bis carbonate (BTBC) was prepared from 1-hydroxy-6-trifluoromethylbenzotriazole and trichloromethyl chloroformate (trichloromethyl carbonochloridate).The reaction of BTBC and alcohols afforded the corresponding acti
SELECTIVE TRANSFORMATION OF N-t-BUTOXYCARBONYL GROUP INTO N-ALKOXYCARBONYL GROUP via N-CARBOXYLATE ION EQUIVALENT
Sakaitani, Masahiro,Ohfune, Yasufumi
, p. 5543 - 5546 (2007/10/02)
Reaction of a variety of N-t-butoxycarbonyl compounds with t-butyldimethylsilyl trifluoromethanesulfonate afforded the N-t-butyldimethylsilyloxycarbonyl compounds, chemoselectively, which upon treatment with an alkyl or aryl halide provided the corresponding N-alkoxy- or N-aryloxycarbonyl compounds, efficiently.
