Efficient phosphine ligands for the one-pot palladium-catalyzed borylation/Suzuki–Miyaura cross-coupling reaction

2015 ◽  
Vol 13 (11) ◽  
pp. 3236-3242 ◽  
Author(s):  
You Chen ◽  
Hui Peng ◽  
Yun-Xiao Pi ◽  
Tong Meng ◽  
Ze-Yu Lian ◽  
...  
Keyword(s):  
Coupling Reaction ◽  
Cross Coupling ◽  
Phosphine Ligands ◽  
One Pot ◽  
Cross Coupling Reaction ◽  
Palladium Catalyzed ◽  
The One

An air-stable 2-(anthracen-9-yl)-1H-inden-3-yl dicyclohexylphosphine was used in palladium-catalyzed borylation/Suzuki–Miyaura cross-coupling reaction.

ChemInform Abstract: Efficient Phosphine Ligands for the One-Pot Palladium-Catalyzed Borylation/Suzuki-Miyaura Cross-Coupling Reaction.

ChemInform ◽  
2015 ◽  
Vol 46 (28) ◽  
pp. no-no
Author(s):  
You Chen ◽  
Hui Peng ◽  
Yun-Xiao Pi ◽  
Tong Meng ◽  
Ze-Yu Lian ◽  
...  
Keyword(s):  
Coupling Reaction ◽  
Cross Coupling ◽  
Phosphine Ligands ◽  
One Pot ◽  
Cross Coupling Reaction ◽  
Palladium Catalyzed ◽  
The One

ChemInform Abstract: Palladium-Catalyzed Cross-Coupling Reaction of N-Alkoxyimidoyl Bromides and Its Application to One-Pot Synthesis of N-Arylamines.

ChemInform ◽  
2012 ◽  
Vol 43 (9) ◽  
pp. no-no
Author(s):  
Masafumi Ueda ◽  
Shoichi Sugita ◽  
Naoki Aoi ◽  
Aoi Sato ◽  
Yuki Ikeda ◽  
...  
Keyword(s):  
Coupling Reaction ◽  
Cross Coupling ◽  
One Pot ◽  
One Pot Synthesis ◽  
Cross Coupling Reaction ◽  
Palladium Catalyzed

One-Pot Palladium-Catalyzed Cross-Coupling Reaction of Aryl Iodides with Stannylarsanes and Stannylstibanes

2003 ◽  
Vol 5 (15) ◽  
pp. 2731-2734 ◽  
Author(s):  
Mariana Bonaterra ◽  
Sandra E. Martín ◽  
Roberto A. Rossi
Keyword(s):  
Coupling Reaction ◽  
Cross Coupling ◽  
One Pot ◽  
Aryl Iodides ◽  
Cross Coupling Reaction ◽  
Palladium Catalyzed

One-pot synthesis of benzoxaborole derivatives from the palladium-catalyzed cross-coupling reaction of alkoxydiboron with unprotected o-bromobenzylalcohols

2015 ◽  
Vol 13 (46) ◽  
pp. 11362-11368 ◽  
Author(s):  
Jianan Zhu ◽  
Ying Wei ◽  
Dongqing Lin ◽  
Changjin Ou ◽  
Linghai Xie ◽  
...  
Keyword(s):  
Coupling Reaction ◽  
Cross Coupling ◽  
One Pot ◽  
Mild Conditions ◽  
One Pot Synthesis ◽  
Cross Coupling Reaction ◽  
Palladium Catalyzed

Under very mild conditions, functionalized benzoxaborole derivatives were prepared in good to excellent yields via a palladium-catalyzed Miyaura borylation reaction of readily available unprotected o-bromobenzylalcohols, and bis(pinacolato)diboron (B2pin2) without the assistance of an acid.

scholarly journals Palladium-Catalyzed Cross Coupling Reaction of N-Alkoxyimidoyl Bromides and Its Application to One-Pot Synthesis of N-Arylamines

2011 ◽  
Vol 59 (9) ◽  
pp. 1206-1208 ◽  
Author(s):  
Masafumi Ueda ◽  
Shoichi Sugita ◽  
Naoki Aoi ◽  
Aoi Sato ◽  
Yuki Ikeda ◽  
...  
Keyword(s):  
Coupling Reaction ◽  
Cross Coupling ◽  
One Pot ◽  
One Pot Synthesis ◽  
Cross Coupling Reaction ◽  
Palladium Catalyzed

Synthesis of Internal Alkynes through an Effective Tandem ­Elimination–Hydrodebromination–Cross-Coupling of gem-­Dibromoalkenes with Halobenzenes

Synlett ◽  
2017 ◽  
Vol 29 (02) ◽  
pp. 209-214 ◽  
Author(s):  
Yuan Ji ◽  
Ning Zhong ◽  
Zinan Kang ◽  
Guobing Yan ◽  
Ming Zhao
Keyword(s):  
Coupling Reaction ◽  
Cross Coupling ◽  
Sonogashira Coupling ◽  
Reaction Conditions ◽  
One Pot ◽  
Cross Coupling Reaction ◽  
Sonogashira Coupling Reaction ◽  
Palladium Catalyzed ◽  
Internal Alkyne

Carbon–carbon couplings are among the most important strategies for constructing functional molecules in organic synthetic chemistry, and cheap, diverse, and readily available coupling partners are crucial to these diverse reactions. In this contribution, we report the first palladium-catalyzed C–C cross-coupling reaction of two kinds of organic halide, a gem-dibromoalkene and a halobenzene, as the starting materials. Terminal alkynes were generated in situ through a tandem elimination–hydrodebromination process, and the internal alkyne final products were synthesized in one pot. The reaction proceeded under simple, facile, and classic copper-free Sonogashira coupling reaction conditions in good to excellent yields.

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