scholarly journals One-pot palladium-catalyzed synthesis of sulfonyl fluorides from aryl bromides

2017 ◽  
Vol 8 (2) ◽  
pp. 1233-1237 ◽  
Author(s):  
Alyn T. Davies ◽  
John M. Curto ◽  
Scott W. Bagley ◽  
Michael C. Willis
Keyword(s):  
Palladium Catalysis ◽  
Efficient Synthesis ◽  
One Pot ◽  
Aryl Bromides ◽  
Palladium Catalyzed

A mild, efficient synthesis of sulfonyl fluorides from aryl and heteroaryl bromides utilizing palladium catalysis is described.

scholarly journals Asymmetric synthesis of chiral cycloalkenone derivatives via palladium catalysis

2014 ◽  
Vol 5 (4) ◽  
pp. 1354-1360 ◽  
Author(s):  
Barry M. Trost ◽  
James T. Masters ◽  
Jean-Philip Lumb ◽  
Dahlia Fateen
Keyword(s):  
Natural Products ◽  
Asymmetric Synthesis ◽  
Palladium Catalysis ◽  
Building Blocks ◽  
Efficient Synthesis ◽  
Palladium Catalyzed

Palladium-catalyzed oxidative desymmetrization enables the efficient synthesis of both enantioenriched cycloalkenone building blocks and diverse epoxyquinoid natural products.

Palladium-catalyzed one-pot Catellani reaction: An efficient synthesis of α-alkynyl aromatic ketones via ortho acylation and ipso alkynylation

Tetrahedron ◽  
2018 ◽  
Vol 74 (40) ◽  
pp. 5942-5949 ◽  
Author(s):  
Shao-Peng Yu ◽  
Yue Zhong ◽  
Ting Gu ◽  
Wen-Yu Wu ◽  
Tian-Yuan Fan ◽  
...  
Keyword(s):  
Efficient Synthesis ◽  
One Pot ◽  
Aromatic Ketones ◽  
Palladium Catalyzed

Cross-coupling reactivity of 1,1-dichloroalkenes under palladium catalysis: domino synthesis of diarylalkynes

2018 ◽  
Vol 42 (6) ◽  
pp. 4412-4418 ◽  
Author(s):  
L. N. Rao Maddali ◽  
Suresh Meka
Keyword(s):  
Palladium Catalysis ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Efficient Synthesis ◽  
Cross Coupling Reaction ◽  
Palladium Catalyzed

An efficient synthesis of diarylalkynes was achieved from the domino cross-coupling reaction of 1,1-dichloroalkenes with triarylbismuth reagents under palladium-catalyzed conditions.

scholarly journals Palladium-Catalyzed Denitrative Mizoroki–Heck Reaction

2020 ◽  
Author(s):  
Toshimasa Okita ◽  
Kitty K. Asahara ◽  
Kei Muto ◽  
Junichiro Yamaguchi
Keyword(s):  
Heck Reaction ◽  
Palladium Catalysis ◽  
Product Yield ◽  
Nucleophilic Aromatic Substitution ◽  
Aromatic Substitution ◽  
One Pot ◽  
Palladium Catalyzed

<div><p>We have developed a Mizoroki–Heck reaction of nitroarenes with alkenes under palladium catalysis. The use of a Pd/BrettPhos catalyst promoted the alkenylation, whereas other catalysts led to a decrease in the product yield. In addition to nitroarenes, nitroheteroarenes were also applicable to the present reaction. Combination of a nucleophilic aromatic substitution (S<sub>N</sub>Ar) with the denitrative alkenylation produced a multi-functionalized arene in a one-pot operation.</p></div>

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