4.5 Review

Development of green methodologies for Heck, Chan-Lam, Stille and Suzuki cross-coupling reactions

Related references

Note: Only part of the references are listed.
Review Biochemistry & Molecular Biology

Synthetic applications and methodology development of Chan-Lam coupling: a review

Iqra Munir et al.

MOLECULAR DIVERSITY (2019)

Article Chemistry, Multidisciplinary

An efficient palladium catalyzed Mizoroki-Heck cross-coupling in water

Sanjay N. Jadhav et al.

GREEN CHEMISTRY (2017)

Article Biochemistry & Molecular Biology

Synthesis of Pd(0) nanocatalyst using lignin in water for the Mizoroki-Heck reaction under solvent-free conditions

M. B. Marulasiddeshwara et al.

INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES (2016)

Article Chemistry, Organic

Matsuda-Heck reaction with arenediazonium tosylates in water

Ksenia V. Kutonova et al.

BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY (2015)

Article Chemistry, Organic

A transition-metal-free Heck-type reaction between alkenes and alkyl iodides enabled by light in water

Wenbo Liu et al.

ORGANIC & BIOMOLECULAR CHEMISTRY (2015)

Article Chemistry, Multidisciplinary

Microwave-promoted solventless Mizoroki-Heck reactions catalysed by Pd nanoparticles supported on laponite clay

Alejandro V. Martinez et al.

RSC ADVANCES (2015)

Article Chemistry, Multidisciplinary

Microwave-Assisted Synthesis of 5-Phenyl-2-hydroxyacetophenone Derivatives by a Green Suzuki Coupling Reaction

Pedro Soares et al.

JOURNAL OF CHEMICAL EDUCATION (2015)

Article Chemistry, Inorganic & Nuclear

PEG-modified N-heterocyclic carbene ligands for highly efficient and recyclable Pd-catalyzed Heck reaction in water

Yulan Liu et al.

TRANSITION METAL CHEMISTRY (2014)

Article Chemistry, Multidisciplinary

Cyclic Carbonates as Green Alternative Solvents for the Heck Reaction

Helen L. Parker et al.

ACS SUSTAINABLE CHEMISTRY & ENGINEERING (2014)

Article Chemistry, Physical

Silica-supported PEI capped nanopalladium as potential catalyst in Suzuki, Heck and Sonogashira coupling reactions

Pitchaimani Veerakumar et al.

APPLIED CATALYSIS A-GENERAL (2013)

Article Chemistry, Multidisciplinary

Stille couplings in water at room temperature

Guo-Ping Lu et al.

GREEN CHEMISTRY (2013)

Article Chemistry, Multidisciplinary

An Operationally Simple Aqueous Suzuki-Miyaura Cross-Coupling Reaction for an Undergraduate Organic Chemistry Laboratory

Alaina E. Hamilton et al.

JOURNAL OF CHEMICAL EDUCATION (2013)

Article Chemistry, Multidisciplinary

Transforming Suzuki-Miyaura Cross-Couplings of MIDA Boronates into a Green Technology: No Organic Solvents

Nicholas A. Isley et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2013)

Article Chemistry, Organic

Nickel-Catalyzed Suzuki-Miyaura Couplings in Green Solvents

Stephen D. Ramgren et al.

ORGANIC LETTERS (2013)

Article Chemistry, Organic

Heck-Matsuda reaction of arenediazonium salts in water

Jordi Salabert et al.

TETRAHEDRON (2013)

Article Chemistry, Organic

A novel N-O ligand for palladium-catalyzed Mizoroki-Heck reaction in neat water

Yufang Wang et al.

TETRAHEDRON LETTERS (2013)

Article Chemistry, Organic

Ligand-free C-N bond formation in aqueous medium using a reusable Cu-Mn bimetallic catalyst

Sanghapal D. Sawant et al.

TETRAHEDRON LETTERS (2013)

Article Chemistry, Applied

Accelerated Heck reaction using ortho-palladated complex with controlled microwave heating

Abdol R. Hajipour et al.

APPLIED ORGANOMETALLIC CHEMISTRY (2009)

Article Chemistry, Multidisciplinary

An efficient aqueous microwave-assisted Suzuki-Miyaura cross-coupling reaction in the thiazole series

Anita Cohen et al.

GREEN CHEMISTRY (2009)

Article Chemistry, Multidisciplinary

A Convenient Catalyst for Aqueous and Protein Suzuki-Miyaura Cross-Coupling

Justin M. Chalker et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2009)

Review Chemistry, Multidisciplinary

Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling Reactions Employing Dialkylbiaryl Phosphine Ligands

Ruben Martin et al.

ACCOUNTS OF CHEMICAL RESEARCH (2008)