Investigations into the Pd-catalysed cross-coupling of phenylacetylene with aryl chlorides: simple one-pot procedure and the effect of ZnCl2 co-catalysisElectronic supplementary information (ESI) available: general experimental, procedure for cross-coupling experiments and characterization data for products. See http://www.rsc.org/suppdata/cc/b2/b200453b/

2002 ◽  
pp. 818-819 ◽  
Author(s):  
Michael R. Eberhard ◽  
Zhaohui Wang ◽  
Craig M. Jensen
2018 ◽  
Vol 5 (22) ◽  
pp. 3319-3323 ◽  
Author(s):  
Xinyu Duan ◽  
Pengbin Li ◽  
Guirong Zhu ◽  
Chunling Fu ◽  
Qin Chen ◽  
...  

With the readily available Gorlos-Phos as a ligand, unsymmetrical biaryls were prepared efficiently from Pd-catalyzed one-pot two-step cross-coupling of two different aryl chlorides in the presence of B2Pin2.


2020 ◽  
Vol 40 (10) ◽  
pp. 3338
Author(s):  
Man Pan Leung ◽  
Chung Chiu Yeung ◽  
Pui Ying Choy ◽  
Chau Ming So ◽  
Fuk Yee Kwong

ChemInform ◽  
2009 ◽  
Vol 40 (5) ◽  
Author(s):  
Shohei Sase ◽  
Milica Jaric ◽  
Albrecht Metzger ◽  
Vladimir Malakhov ◽  
Paul Knochel

RSC Advances ◽  
2014 ◽  
Vol 4 (62) ◽  
pp. 32643-32646 ◽  
Author(s):  
Kai Xu ◽  
Suyan Sun ◽  
Guodong Zhang ◽  
Fan Yang ◽  
Yangjie Wu

Synthesis of unsymmetrical diarylacetylenes via one-pot Sonogashira/Deacetonation/Sonogashira cross-coupling of two different aryl chlorides with 2-methyl-3-butyn-2-ol was developed.


RSC Advances ◽  
2018 ◽  
Vol 8 (25) ◽  
pp. 13643-13648 ◽  
Author(s):  
Hong Ji ◽  
Li-Yang Wu ◽  
Jiang-Hong Cai ◽  
Guo-Rong Li ◽  
Na-Na Gan ◽  
...  

A highly efficient room-temperature strategy for borylation and one-pot two-step borylation/Suzuki–Miyaura cross-coupling reaction of aryl chlorides have been developed.


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