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Green synthesis of new pyrrolidine-fused spirooxindoles via three-component domino reaction in EtOH/H2O.


ABSTRACT: An efficient, green and sustainable approach for the synthesis of novel polycyclic pyrrolidine-fused spirooxindole compounds was developed. The synthesis included a one-pot, three-component, domino reaction of (E)-3-(2-nitrovinyl)-indoles, isatins and chiral polycyclic α-amino acids under catalyst-free conditions at room temperature in EtOH-H2O. The salient features of this methodology are eco-friendliness, high yields and the ease of obtaining target compounds without the involvement of toxic solvents and column chromatography. These novel polycyclic pyrrolidine-fused spirooxindoles provide a collection of structurally diverse compounds that show promise for future bioassays and medical treatments.

SUBMITTER: Wang YC 

PROVIDER: S-EPMC9078157 | biostudies-literature | 2018 Feb

REPOSITORIES: biostudies-literature

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Green synthesis of new pyrrolidine-fused spirooxindoles <i>via</i> three-component domino reaction in EtOH/H<sub>2</sub>O.

Wang Yong-Chao YC   Wang Jun-Liang JL   Burgess Kevin S KS   Zhang Jiang-Wei JW   Zheng Qiu-Mei QM   Pu Ya-Dan YD   Yan Li-Jun LJ   Chen Xue-Bing XB  

RSC advances 20180202 11


An efficient, green and sustainable approach for the synthesis of novel polycyclic pyrrolidine-fused spirooxindole compounds was developed. The synthesis included a one-pot, three-component, domino reaction of (<i>E</i>)-3-(2-nitrovinyl)-indoles, isatins and chiral polycyclic α-amino acids under catalyst-free conditions at room temperature in EtOH-H<sub>2</sub>O. The salient features of this methodology are eco-friendliness, high yields and the ease of obtaining target compounds without the invo  ...[more]

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