34944-23-5Relevant academic research and scientific papers
Oxoarylation of ynamides with N-aryl hydroxamic acids
Chen, Changwei,Zhang, Hongyu,Xu, Gang,Cui, Sunliang
, p. 2551 - 2554 (2021/03/17)
Ynamides are electron-rich alkynes with unique reactivities and act as flexible building blocks in organic synthesis. Therefore, the investigation for transformation of ynamides with exceptional selectivity and efficiency is attractive and interesting. He
Synthesis of oxindole from acetanilide via Ir(iii)-catalyzed C-H carbenoid functionalization
Patel, Pitambar,Borah, Gongutri
supporting information, p. 443 - 446 (2017/01/03)
Herein we disclose the first report on the synthesis of oxindole derivatives from acetanilide via Ir(iii)-catalyzed intermolecular C-H functionalization with diazotized Meldrum's acid. A broad range of substituted anilides were found to react smoothly under the Ir(iii)-catalytic system to afford the corresponding N-protected oxindoles. The N-protecting groups, such as Ac, Bz or Piv, can be easily removed to furnish the oxindole. Various synthetic applications of the synthesized oxindole were also demonstrated.
COMPOUND; TAUTOMER AND GEOMETRIC ISOMER THEREOF; SALT OF SAID COMPOUND, TAUTOMER, OR GEOMETRIC ISOMER; METHOD FOR MANUFACTURING SAID COMPOUND, TAUTOMER, ISOMER, OR SALT; ANTIMICROBIAL AGENT; AND ANTI-INFECTIVE DRUG
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Paragraph 0167-0168; 0173, (2015/09/23)
A compound represented by any one of General Formulas (1) to (5), a tautomer or geometric isomer thereof, or a salt thereof.
