Correction: Efficient in situ N-heterocyclic carbene palladium(ii) generated from Pd(OAc)2 catalysts for carbonylative Suzuki coupling reactions of arylboronic acids with 2-bromopyridine under inert conditions leading to unsymmetrical arylpyridine ketones: synthesis, characterization and cytotoxic activities

Nedra Touj; Abdullah S. Al-Ayed; Mathieu Sauthier; Lamjed Mansour; Abdel Halim Harrath; Jameel Al-Tamimi; Ismail ?zdemir; Sedat Ya?ar; Naceur Hamdi

首页> 外文期刊>RSC Advances >Correction: Efficient in situ N-heterocyclic carbene palladium(ii) generated from Pd(OAc)2 catalysts for carbonylative Suzuki coupling reactions of arylboronic acids with 2-bromopyridine under inert conditions leading to unsymmetrical arylpyridine ketones: synthesis, characterization and cytotoxic activities

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Correction: Efficient in situ N-heterocyclic carbene palladium(ii) generated from Pd(OAc)2 catalysts for carbonylative Suzuki coupling reactions of arylboronic acids with 2-bromopyridine under inert conditions leading to unsymmetrical arylpyridine ketones: synthesis, characterization and cytotoxic activities

机译：更正：由Pd（OAc）2催化剂生成的高效原位N-杂环卡宾钯（ii）在惰性条件下导致芳基硼酸与2-溴吡啶的羰基Suzuki偶联反应，导致不对称的芳基吡啶酮：合成，表征和细胞毒性

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Correction for ‘Efficient in situ N-heterocyclic carbene palladium( II ) generated from Pd(OAc) _(2) catalysts for carbonylative Suzuki coupling reactions of arylboronic acids with 2-bromopyridine under inert conditions leading to unsymmetrical arylpyridine ketones: synthesis, characterization and cytotoxic activities’ by Nedra Touj et al. , RSC Adv. , 2018, 8 , 40000–40015.

机译：由Pd（OAc）_（2）催化剂生成的高效原位N-杂环卡宾钯（II）的校正，用于在惰性条件下导致芳基硼酸与2-溴吡啶的羰基化Suzuki偶联反应，导致不对称的芳基吡啶酮：合成，表征和Nedra Touj等人的“细胞毒活性”。，RSC Adv。，2018，8，40000–40015。

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《RSC Advances》 |2019年第2期|共1页
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Nedra Touj; Abdullah S. Al-Ayed; Mathieu Sauthier; Lamjed Mansour; Abdel Halim Harrath; Jameel Al-Tamimi; Ismail ?zdemir; Sedat Ya?ar; Naceur Hamdi;
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1. Correction: Efficient in situ N-heterocyclic carbene palladium(ii) generated from Pd(OAc)2 catalysts for carbonylative Suzuki coupling reactions of arylboronic acids with 2-bromopyridine under inert conditions leading to unsymmetrical arylpyridine ketones: synthesis, characterization and cytotoxic activities [J] . Nedra Touj, Abdullah S. Al-Ayed, Mathieu Sauthier, RSC Advances . 2019,第2期

机译：更正：由Pd（OAc）2催化剂生成的高效原位N-杂环卡宾钯（ii）在惰性条件下导致芳基硼酸与2-溴吡啶的羰基Suzuki偶联反应，导致不对称的芳基吡啶酮：合成，表征和细胞毒性
2. Efficient in situ N-heterocyclic carbene palladium(ii) generated from Pd(OAc)(2) catalysts for carbonylative Suzuki coupling reactions of arylboronic acids with 2-bromopyridine under inert conditions leading to unsymmetrical arylpyridine ketones: synthesis, characterization and cytotoxic activities (vol 8, pg 40000, 2018) [J] . Touj Nedra, Al-Ayed Abdullah S., Sauthier Mathieu, RSC Advances . 2019,第2期

机译：高效的原位N-杂环钯（II）从Pd（OAC）（2）碳酸苏氏氧化芳基偶联反应与2-溴吡啶的羰基·铃木偶联反应，导致非对称芳基吡啶酮：合成，表征和细胞毒性活性（Vol 8，PG 40000，2018）
3. Efficient in situ N-heterocyclic carbene palladium(ii) generated from Pd(OAc)(2) catalysts for carbonylative Suzuki coupling reactions of arylboronic acids with 2-bromopyridine under inert conditions leading to unsymmetrical arylpyridine ketones: synthesis, characterization and cytotoxic activities [J] . Touj Nedra, Al-Ayed Abdullah S., Sauthier Mathieu, RSC Advances . 2018,第70期

机译：高效的原位正杂环钯（II）由Pd（OAC）（2）催化剂产生的芳族氨基酸含有2-溴吡啶的羰基铃木偶联反应，其惰性条件导致非对称芳基吡啶酮：合成，表征和细胞毒性活性
4. Suzuki–Miyaura cross-coupling reaction of 1-aryltriazenes with arylboronic acids catalyzed by a recyclable polymer-supported N-heterocyclic carbene–palladium complex catalyst [O] . Guangming Nan, Fang Ren, Meiming Luo 2010

机译：可回收的聚合物负载的N-杂环卡宾-钯配合物催化的1-芳基三氮烯与芳基硼酸的铃木-宫浦交叉偶联反应
5. Correction: Efficient in situ N-heterocyclic carbene palladium(ii) generated from Pd(OAc)2 catalysts for carbonylative Suzuki coupling reactions of arylboronic acids with 2-bromopyridine under inert conditions leading to unsymmetrical arylpyridine ketones: synthesis, characterization and cytotoxic activities [O] . Nedra Touj, Abdullah S. Al-Ayed, Mathieu Sauthier, 2019

机译：校正：从Pd（OAC）2催化剂中产生的芳基氨基酸的2-溴苯酸偶联反应的羰基酸胆碱偶联反应的高效惰性条件，导致非对称芳基吡啶酮：合成，表征和细胞毒性活性

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