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Palladium-catalyzed multi-acetoxylation of 1,3-disubstituted 1H-pyrazole-5-carboxylates via direct C(sp^2)-H or C(sp^3)-H bond activation 被引量:1

Palladium-catalyzed multi-acetoxylation of 1,3-disubstituted 1H-pyrazole-5-carboxylates via direct C(sp^2)-H or C(sp^3)-H bond activation
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摘要 A palladium-catalyzed multi-acetoxylation of 1,3-disubstituted 1H-pyrazole-5-carboxylate derivatives containing multiple potential reactive sites is described. Therein, the sequence of this process has been appropriately investigated. The protocol mainly provides the di- and tri-acetoxylated products for 1,3- diarylpyrazoles. Besides, it is found that the acetoxylation of C(sp3)-H bond is prior to that of C(sp2)-H bond under structurally competitive conditions. A palladium-catalyzed multi-acetoxylation of 1,3-disubstituted 1H-pyrazole-5-carboxylate derivatives containing multiple potential reactive sites is described. Therein, the sequence of this process has been appropriately investigated. The protocol mainly provides the di- and tri-acetoxylated products for 1,3- diarylpyrazoles. Besides, it is found that the acetoxylation of C(sp3)-H bond is prior to that of C(sp2)-H bond under structurally competitive conditions.
机构地区 School of Pharmacy
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 2016年第10期1617-1621,共5页 中国化学快报(英文版)
基金 the National Natural Science Foundation of China(Nos.21176074 and 21476074) the Research Fund for the Doctoral Program of Higher Education of China(No.20130074110009)for financial support
关键词 Palladium catalysisFunctionalized pyrazolesMulti-acetoxylationC-H activationMonodentate directing group Palladium catalysisFunctionalized pyrazolesMulti-acetoxylationC-H activationMonodentate directing group
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