ChemInform Abstract: Synthesis of Symmetrical and Unsymmetrical Diarylalkynes from Propiolic Acid Using Palladium-Catalyzed Decarboxylative Coupling.

ChemInform ◽  
2010 ◽  
Vol 42 (3) ◽  
pp. no-no
Author(s):  
Kyungho Park ◽  
Goun Bae ◽  
Jeongju Moon ◽  
Jaehoon Choe ◽  
Kwang Ho Song ◽  
...  
2010 ◽  
Vol 75 (18) ◽  
pp. 6244-6251 ◽  
Author(s):  
Kyungho Park ◽  
Goun Bae ◽  
Jeongju Moon ◽  
Jaehoon Choe ◽  
Kwang Ho Song ◽  
...  

Synthesis ◽  
2018 ◽  
Vol 50 (16) ◽  
pp. 3197-3204 ◽  
Author(s):  
Kwang Song ◽  
Sunwoo Lee ◽  
Jaerim Park

Arylsulfonyl hydrazides were employed as coupling partners for the decarboxylative coupling reaction of propiolic acid derivatives. When the reaction was conducted using Pd(TFA)2 (1.0 mol%), dppp (1.0 mol%), and Cu(OAc)2 (2.4 equiv) in DMF at 100 °C for 0.5 hour, the desired coupled products were formed in moderate to good yields. The reaction showed good tolerance toward functional groups such as ester, ketone, cyano, nitro, chloro, and bromo groups.


2014 ◽  
Vol 10 ◽  
pp. 384-393 ◽  
Author(s):  
Andrea Caporale ◽  
Stefano Tartaggia ◽  
Andrea Castellin ◽  
Ottorino De Lucchi

Two efficient protocols for the palladium-catalyzed synthesis of aryl-2-methyl-3-butyn-2-ols from aryl bromides in the absence of copper were developed. A simple catalytic system consisting of Pd(OAc)2 and P(p-tol)3 using DBU as the base and THF as the solvent was found to be highly effective for the coupling reaction of 2-methyl-3-butyn-2-ol (4) with a wide range of aryl bromides in good to excellent yields. Analogously, the synthesis of aryl-2-methyl-3-butyn-2-ols was performed also through the decarboxylative coupling reaction of 4-hydroxy-4-methyl-2-pentynoic acid with aryl bromides, using a catalyst containing Pd(OAc)2 in combination with SPhos or XPhos in the presence of tetra-n-butylammonium fluoride (TBAF) as the base and THF as the solvent. Therefore, new efficient approaches to the synthesis of terminal acetylenes from widely available aryl bromides rather than expensive iodides and using 4 or propiolic acid rather than TMS-acetylene as inexpensive alkyne sources are described.


ChemInform ◽  
2014 ◽  
Vol 45 (39) ◽  
pp. no-no
Author(s):  
Takashi Mino ◽  
Eri Yoshizawa ◽  
Kohei Watanabe ◽  
Taichi Abe ◽  
Kiminori Hirai ◽  
...  

2013 ◽  
Vol 355 (4) ◽  
pp. 705-710 ◽  
Author(s):  
Police Vishnuvardhan Reddy ◽  
Pottabathula Srinivas ◽  
Manne Annapurna ◽  
Suresh Bhargava ◽  
Jorg Wagler ◽  
...  

ChemInform ◽  
2015 ◽  
Vol 46 (51) ◽  
pp. no-no
Author(s):  
Miles Kenny ◽  
Jeppe Christensen ◽  
Simon J. Coles ◽  
Vilius Franckevicius

2016 ◽  
Vol 57 (41) ◽  
pp. 4581-4584 ◽  
Author(s):  
Jisun Jang ◽  
Gabriel Charles Edwin Raja ◽  
Ju-Hyeon Lee ◽  
Yujeong Son ◽  
Jimin Kim ◽  
...  

2017 ◽  
Vol 38 (11) ◽  
pp. 1368-1371 ◽  
Author(s):  
Ju-Hyeon Lee ◽  
Gabriel Charles Edwin Raja ◽  
Jimin Kim ◽  
Kye Chun Nam ◽  
Sunwoo Lee

2011 ◽  
Vol 52 (5) ◽  
pp. 576-580 ◽  
Author(s):  
Kyungho Park ◽  
Goun Bae ◽  
Ahbyeol Park ◽  
Yong Kim ◽  
Jaehoon Choe ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document