ChemInform Abstract: Highly Selective Cross-Coupling Reactions of Organosilicon Compounds Mediated by Fluoride Ion and a Palladium Catalyst

Pyridinyl functionalized MCM-48-supported Pd-catalyst efficiently (0.013–0.025 mol%) promoted Heck, Suzuki and Sonogashira cross-coupling reactions. Moreover, the catalyst was reused five times without significant loss of its activity.

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ChemInform Abstract: NaOH-Promoted Cross-Coupling Reactions of Organosilicon Compounds with Organic Halides: Practical Routes to Biaryls, Alkenylarenes and Conjugated Dienes.

ChemInform ◽

10.1002/chin.199720060 ◽

2010 ◽

Vol 28 (20) ◽

pp. no-no

Author(s):

E. HAGIWARA ◽

K. GOUDA ◽

Y. HATANAKA ◽

T. HIYAMA

Keyword(s):

Cross Coupling ◽

Conjugated Dienes ◽

Coupling Reactions ◽

Organosilicon Compounds ◽

Cross Coupling Reactions ◽

Organic Halides

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Porous polymer supported palladium catalyst for cross coupling reactions with high activity and recyclability

Science China Chemistry ◽

10.1007/s11426-011-4491-8 ◽

2012 ◽

Vol 55 (10) ◽

pp. 2095-2103 ◽

Cited By ~ 12

Author(s):

Qi Sun ◽

LongFeng Zhu ◽

ZhenHua Sun ◽

XiangJu Meng ◽

Feng-Shou Xiao

Keyword(s):

High Activity ◽

Palladium Catalyst ◽

Cross Coupling ◽

Porous Polymer ◽

Coupling Reactions ◽

Supported Palladium Catalyst ◽

Cross Coupling Reactions ◽

Supported Palladium ◽

Polymer Supported

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Highly active and recyclable silica gel-supported palladium catalyst for mild cross-coupling reactions of unactivated heteroaryl chlorides

Green Chemistry ◽

10.1039/c0gc00251h ◽

2010 ◽

Vol 12 (11) ◽

pp. 2024 ◽

Cited By ~ 59

Author(s):

Dong-Hwan Lee ◽

Ji-Young Jung ◽

Myung-Jong Jin

Keyword(s):

Silica Gel ◽

Palladium Catalyst ◽

Cross Coupling ◽

Coupling Reactions ◽

Supported Palladium Catalyst ◽

Cross Coupling Reactions ◽

Highly Active ◽

Supported Palladium

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Pd-Catalyzed one-pot sequential cross-coupling reactions of tetrabromothiophene

Organic & Biomolecular Chemistry ◽

10.1039/c7ob02601c ◽

2017 ◽

Vol 15 (48) ◽

pp. 10289-10298 ◽

Cited By ~ 5

Author(s):

Kapil Mohan Saini ◽

Rakesh K. Saunthwal ◽

Akhilesh K. Verma

Keyword(s):

Palladium Catalyst ◽

Cross Coupling ◽

Coupling Reactions ◽

Arylboronic Acid ◽

One Pot ◽

Cross Coupling Reactions ◽

Sterically Hindered

Unsymmetrical one-pot sequential cross-coupling reactions of sterically hindered tetrabromothiophene with arylboronic acid and an alkyne/alkene to afford selective bi-, tri-, and tetrasubstituted aryl/alkynyl-thiophenes with the aid of a palladium catalyst were described.

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