Literature DB >> 26677092

An unprecedented protocol for the synthesis of 3-hydroxy-3-phenacyloxindole derivatives with indolin-2-ones and α-substituted ketones.

Mei Bai1, Yong You, Yong-Zheng Chen, Guang-Yan Xiang, Xiao-Ying Xu, Xiao-Mei Zhang, Wei-Cheng Yuan.   

Abstract

An unprecedented reaction between indolin-2-ones and α-substituted ketones has been developed. Using this protocol, a wide range of biologically important 3-hydroxy-3-phenacyloxindole derivatives could be obtained in good yield (up to 93%) under mild reaction conditions. A possible mechanism of this reaction was tentatively proposed based on some control experiments and MS spectrometry analysis.

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Year:  2015        PMID: 26677092     DOI: 10.1039/c5ob02391b

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  3 in total

Review 1.  Literature Survey and Further Studies on the 3-Alkylation of N-Unprotected 3-Monosubstituted Oxindoles. Practical Synthesis of N-Unprotected 3,3-Disubstituted Oxindoles and Subsequent Transformations on the Aromatic Ring.

Authors:  Eszter Kókai; Gyula Simig; Balázs Volk
Journal:  Molecules       Date:  2016-12-26       Impact factor: 4.411

2.  Study on the Alkylation Reactions of N(7)-Unsubstituted 1,3-Diazaoxindoles.

Authors:  Eszter Kókai; Judit Halász; András Dancsó; József Nagy; Gyula Simig; Balázs Volk
Journal:  Molecules       Date:  2017-05-19       Impact factor: 4.411

3.  Electrochemical Umpolung C-H Functionalization of Oxindoles.

Authors:  Miryam Pastor; Marie Vayer; Harald Weinstabl; Nuno Maulide
Journal:  J Org Chem       Date:  2021-12-28       Impact factor: 4.354

  3 in total

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