ChemInform Abstract: In situ-Generated Nano-Palladium-Catalyzed Ligand-Free Suzuki-Miyaura Reaction of Potassium Aryltrifluoroborates at Room Temperature.

ChemInform ◽  
2015 ◽  
Vol 46 (37) ◽  
pp. no-no
Author(s):  
Chun Liu ◽  
Xinmin Li ◽  
Zhanming Gao ◽  
Xinnan Wang ◽  
Zilin Jin
Tetrahedron ◽  
2015 ◽  
Vol 71 (23) ◽  
pp. 3954-3959 ◽  
Author(s):  
Chun Liu ◽  
Xinmin Li ◽  
Zhanming Gao ◽  
Xinnan Wang ◽  
Zilin Jin

RSC Advances ◽  
2016 ◽  
Vol 6 (34) ◽  
pp. 28981-28985 ◽  
Author(s):  
Manashi Sarmah ◽  
Anindita Dewan ◽  
Manoj Mondal ◽  
Ashim J. Thakur ◽  
Utpal Bora

The conversion of waste papaya-bark to ash–water extract via low-temperature combustion, and its utilization as an efficient and eco-friendly in situ basic medium for Suzuki–Miyaura cross-coupling reaction at room temperature are reported.


2020 ◽  
Author(s):  
Yuvraj Bhujbal ◽  
kamlesh vadagaonkar ◽  
santosh kori ◽  
Anant Kapdi

A versatile synthetic protocol involving the room temperature direct arylation of benzothiazole with a wide variety of iodo(hetero)arenes under palladium-catalyzed conditions and promoted by HFIP as the reaction solvent has been presented herewith. An in-situ one-pot sequential HFIP promoted selective iodination of (hetero)arenes followed by Pd-catalyzed direct arylation of benzothiazole has also been disclosed. Synthesis of PMX 610 (antitumor agent) analog has been disclosed and also CJM 126 (antitumor agent) has been synthesized.


Molecules ◽  
2018 ◽  
Vol 23 (10) ◽  
pp. 2412 ◽  
Author(s):  
Weijia Shi ◽  
Gang Zou

A highly efficient acylative cross-coupling of trialkylboranes with activated amides has been effected at room temperature to give the corresponding alkyl ketones in good to excellent yields by using 1,3-bis(2,6-diisopropyl)phenylimidazolylidene and 3-chloropyridine co-supported palladium chloride, the PEPPSI catalyst, in the presence of K2CO3 in methyl tert-butyl ether. The scope and limitations of the protocol were investigated, showing good tolerance of acyl, cyano, and ester functional groups in the amide counterpart while halo group competed via the classical Suzuki coupling. The trialkylboranes generated in situ by hydroboration of olefins with BH3 or 9-BBN performed similarly to those separately prepared, making this protocol more practical.


2019 ◽  
Vol 21 (5) ◽  
pp. 995-999 ◽  
Author(s):  
Xinchi Gong ◽  
Jie Wu ◽  
Yunge Meng ◽  
Yulan Zhang ◽  
Long-Wu Ye ◽  
...  

A palladium catalysed Ullmann biaryl synthesis has been developed using hydrazine hydrate as the reducing reagent at room temperature.


2020 ◽  
Author(s):  
Yuvraj Bhujbal ◽  
kamlesh vadagaonkar ◽  
santosh kori ◽  
Anant Kapdi

A versatile synthetic protocol involving the room temperature direct arylation of benzothiazole with a wide variety of iodo(hetero)arenes under palladium-catalyzed conditions and promoted by HFIP as the reaction solvent has been presented herewith. An in-situ one-pot sequential HFIP promoted selective iodination of (hetero)arenes followed by Pd-catalyzed direct arylation of benzothiazole has also been disclosed. Synthesis of PMX 610 (antitumor agent) analog has been disclosed and also CJM 126 (antitumor agent) has been synthesized.


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