22122-89-0Relevant academic research and scientific papers
Synthesis of novel pyrido[1,2-a]pyrimidine-3-carboxamide derivatives and their anticancer activity
Kumar, Gautham Santhosh,Dev, Gaddameedi Jitender,Kumar, Nagiri Ravi,Swaroop, Desireddy Krishna,Chandra, Yedla Poorna,Kumar, Chityala Ganesh,Narsaiah, Banda
, p. 584 - 590 (2015)
A series of novel pyrido[1,2-a]pyrimidine-3-carboxamide derivatives 6a-n were prepared starting from 2(1H) pyridone 1 via hydrolysis, de-carboxylation, selective O-alkylation followed by rearrangement to give pyridine-2-amine 3. Compound 3 on reaction wit
Design, synthesis and biological evaluation of benzimidazole-pyridine-piperidine hybrids as a new class of potent antimicrobial agents
Beulah, KothapallY.,Kumar, Akula Ravi,Lingaiah, Boddupally Peda Venkat,Rao, Pamulaparthy Shanthan,Narsaiah, Banda,Reddy, Aaramadaka Sunil Kumar,Murty, Upadhyayula Surya Narayana
, p. 38 - 45 (2015)
A series of novel benzimidazole-pyridine-piperidine hybrids was synthesized in good yields and characterized by spectral and elemental analyses. The compounds 4a-h and 5a-c were evaluated for their in vitro antibacterial activity against gram-positive org
One-Pot Sequential Multistep Transformation of α,β-Unsaturated Trifluoromethyl Ketones: Facile Synthesis of Trifluoromethylated 2-Pyridones
Lv, Ning,Tian, Yi-Qiang,Zhang, Fa-Guang,Ma, Jun-An
supporting information, p. 605 - 609 (2019/03/07)
A one-pot transformation of α,β-unsaturated trifluoromethyl ketones with 2-(phenylsulfinyl)acetamide to give trifluoromethylated 2-pyridones is realized. The reaction proceeds under mild conditions and involves multiple steps in an expeditious and controlled sequence to provide efficient access to a broad range of trifluoromethylated 2-pyridones in moderate to high yields. Moreover, further synthetic manipulations permit the routine synthesis of a diverse array of trifluoromethylated pyridines with good efficiency.
Redox-Divergent Synthesis of Fluoroalkylated Pyridines and 2-Pyridones through Cu-Catalyzed N?O Cleavage of Oxime Acetates
Bai, Dachang,Wang, Xueli,Zheng, Guangfan,Li, Xingwei
supporting information, p. 6633 - 6637 (2018/05/03)
Cu-catalyzed redox-divergent [3+3] coupling of oxime esters with β-CF3 enones and acrylates is described. This redox-neutral coupling with enones and acrylates affords trifluoromethylated pyridines and pyridones, respectively. Under reductive c
Isothiourea-mediated one-pot synthesis of functionalized pyridines
Stark, Daniel G.,Morrill, Louis C.,Yeh, Pei-Pei,Slawin, Alexandra M. Z.,O'Riordan, Timothy J. C.,Smith, Andrew D.
, p. 11642 - 11646 (2013/11/06)
Acids to bases: The synthesis of 2,4,6-trisubstituted pyridines from (phenylthio)acetic acid and a range of α,β-unsaturated ketimines is reported. This process proceeds by intermolecular Michael addition/ lactamization, thiophenol elimination, and N- to O
