One-Pot Palladium-Catalyzed Cross-Coupling Treble of Borylation, the Suzuki Reaction and Amination

2017 ◽  
Vol 359 (4) ◽  
pp. 616-622 ◽  
Author(s):  
Howard Jong ◽  
Stanley T.-C. Eey ◽  
Yee Hwee Lim ◽  
Sangeeta Pandey ◽  
Nurul Azmah Bte Iqbal ◽  
...  
Keyword(s):  
Suzuki Reaction ◽  
Cross Coupling ◽  
One Pot ◽  
Palladium Catalyzed

scholarly journals Highly selective palladium-catalyzed one-pot, five-fold B–H/C–H cross coupling of monocarboranes with alkenes

2019 ◽  
Vol 10 (15) ◽  
pp. 4177-4184 ◽  
Author(s):  
Yunjun Shen ◽  
Kang Zhang ◽  
Xuewei Liang ◽  
Rakesh Dontha ◽  
Simon Duttwyler
Keyword(s):  
Cross Coupling ◽  
One Pot ◽  
Boron Clusters ◽  
Palladium Catalyzed

Palladium-catalyzed five-fold B–H/C–H cross coupling of monocarboranes with alkenes enables the synthesis of selectively penta-functionalized boron clusters.

One-Pot Conversion of Aldehydes and Ketones into 1-Substituted and 1,4-Disubstituted 1,3-Enynes

Synthesis ◽  
2018 ◽  
Vol 50 (17) ◽  
pp. 3307-3321 ◽  
Author(s):  
Jorge Cabezas ◽  
Rebeca Poveda ◽  
José Brenes
Keyword(s):  
Thionyl Chloride ◽  
Cross Coupling ◽  
Sequential Treatment ◽  
Coupling Reactions ◽  
One Pot ◽  
Cross Coupling Reactions ◽  
Tosyl Chloride ◽  
Aldehydes And Ketones ◽  
Palladium Catalyzed

Sequential treatment of 2,3-dichloropropene with magnesium and n-BuLi generates the operational equivalent of 1,3-dilithiopropyne, which upon treatment with aldehydes or ketones, produces the corresponding alkoxy lithium acetylide intermediates. Reaction of this alkoxide with tosyl chloride, and t-BuLi produces 1-substituted, or 1,1-disubstituted 1,3-enynes in a one-pot reaction. When this lithium acetylide intermediates, obtained by this procedure, were used to perform palladium-catalyzed cross-coupling reactions, followed by addition of thionyl chloride and pyridine, 1,4-disubstituted or 1,1,4-trisubstituted 1,3-enynes were obtained in a one-pot protocol.

scholarly journals Facile One-Pot Assembly of New 5-Substituted P,O-Type Indolylphosphine Ligands for Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling of Aryl Chlorides

2020 ◽  
Vol 40 (10) ◽  
pp. 3338
Author(s):  
Man Pan Leung ◽  
Chung Chiu Yeung ◽  
Pui Ying Choy ◽  
Chau Ming So ◽  
Fuk Yee Kwong
Keyword(s):  
Cross Coupling ◽  
One Pot ◽  
Aryl Chlorides ◽  
Palladium Catalyzed

Consecutive Palladium Catalyzed Reactions in One-Pot Reactions

2020 ◽  
Vol 17 (5) ◽  
pp. 559-569
Author(s):  
Ingrid Caroline Vaaland ◽  
Magne Olav Sydnes
Keyword(s):  
Cross Coupling ◽  
Coupling Reactions ◽  
Homogeneous Reaction ◽  
Reaction Conditions ◽  
One Pot ◽  
Cross Coupling Reactions ◽  
Palladium Catalyzed ◽  
Catalyzed Reactions

Combining palladium catalyzed reactions in one-pot reactions represents an efficient and economical use of catalyst. The Suzuki-Miyaura cross-coupling has been proven to be a reaction which can be combined with other palladium catalyzed reactions in the same pot. This mini-review will highlight some of the latest examples where Suzuki-Miyaura cross-coupling reactions have been combined with other palladium catalyzed reactions in one-pot reaction. Predominantly, examples with homogeneous reaction conditions will be discussed in addition to a few examples from the authors where Pd/C have been used as a catalyst.

Directedortho-Metalation–Cross-Coupling Strategies. One-Pot Suzuki Reaction to Biaryl and Heterobiaryl Sulfonamides

2011 ◽  
Vol 13 (14) ◽  
pp. 3588-3591 ◽  
Author(s):  
Cédric Schneider ◽  
Ellen Broda ◽  
Victor Snieckus
Keyword(s):  
Suzuki Reaction ◽  
Cross Coupling ◽  
One Pot ◽  
Coupling Strategies
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