scholarly journals A Robust Pd-Catalyzed C–S Cross-Coupling Process Enabled by Ball-Milling

2020 ◽  
Vol 22 (19) ◽  
pp. 7433-7438
Author(s):  
Andrew C. Jones ◽  
William I. Nicholson ◽  
Harry R. Smallman ◽  
Duncan L. Browne
Keyword(s):  
Ball Milling ◽  
Cross Coupling ◽  
Coupling Process

scholarly journals Correction to “A Robust Pd-Catalyzed C–S Cross-Coupling Process Enabled by Ball-Milling”

2020 ◽  
Vol 22 (21) ◽  
pp. 8746-8746
Author(s):  
Andrew C. Jones ◽  
William I. Nicholson ◽  
Harry R. Smallman ◽  
Duncan L. Browne
Keyword(s):  
Ball Milling ◽  
Cross Coupling ◽  
Coupling Process

ChemInform Abstract: The Preparation of Substituted Pyrazoles from β,β-Dibromo-enones by a Tandem Condensation/Suzuki-Miyaura Cross-Coupling Process.

ChemInform ◽  
2010 ◽  
Vol 41 (27) ◽  
pp. no-no
Author(s):  
Sandra Beltran-Rodil ◽  
Michael G. Edwards ◽  
David S. Pugh ◽  
Mark Reid ◽  
Richard J. K. Taylor
Keyword(s):  
Cross Coupling ◽  
Coupling Process ◽  
Substituted Pyrazoles

scholarly journals Synthesis of Pd Complexes Containing Tailed NHC Ligands and Their Use in a Semicontinuous Membrane-Assisted Suzuki Cross-Coupling Process

2018 ◽  
Vol 22 (11) ◽  
pp. 1509-1517 ◽  
Author(s):  
Dominic Ormerod ◽  
Matthieu Dorbec ◽  
Eugen Merkul ◽  
Nadya Kaval ◽  
Nicolas Lefèvre ◽  
...  
Keyword(s):  
Cross Coupling ◽  
Coupling Process ◽  
Pd Complexes

scholarly journals General Approach to the Total Synthesis of Macroline-Related Sarpagine and Ajmaline Alkaloids1

2008 ◽  
Vol 3 (11) ◽  
pp. 1934578X0800301
Author(s):  
Chitra R. Edwankar ◽  
Rahul V. Edwankar ◽  
Sundari Rallapalli ◽  
James M. Cook
Keyword(s):  
Total Synthesis ◽  
Cross Coupling ◽  
Complex Molecules ◽  
Coupling Process ◽  
Efficient Strategy ◽  
Synthetic Routes

Described in this review is a general and efficient strategy for the synthesis of macroline-related sarpagine and ajmaline alkaloids. The tetracyclic ketone in the parent system, as well as the alkoxy substituted series served as templates for the synthesis of these complex molecules. The palladium-mediated enolate cross coupling process, regiospecific hydroboration, and Tollens reaction are some of the key transformations that have been employed for further functionalization of these templates. Synthetic routes that have been improved, in order to obtain gram quantities of these alkaloids form a part of this review.

Nano-CuFe2O4 as a magnetically separable and reusable catalyst for the synthesis of diaryl/aryl alkyl sulfides via cross-coupling process under ligand-free conditions

2011 ◽  
Vol 9 (17) ◽  
pp. 5989 ◽  
Author(s):  
Kokkirala Swapna ◽  
Sabbavarapu Narayana Murthy ◽  
Mocharla Tarani Jyothi ◽  
Yadavalli Venkata Durga Nageswar
Keyword(s):  
Cross Coupling ◽  
Reusable Catalyst ◽  
Coupling Process ◽  
Ligand Free ◽  
Magnetically Separable

scholarly journals Cu2(BDC)2(BPY)–MOF: an efficient and reusable heterogeneous catalyst for the aerobic Chan–Lam coupling prepared via ball-milling strategy

RSC Advances ◽  
2017 ◽  
Vol 7 (73) ◽  
pp. 46022-46027 ◽  
Author(s):  
Armaqan Khosravi ◽  
Javad Mokhtari ◽  
Mohammad Reza Naimi-Jamal ◽  
Sharareh Tahmasebi ◽  
Leila Panahi
Keyword(s):  
Ball Milling ◽  
Heterogeneous Catalyst ◽  
Boronic Acid ◽  
Aromatic Amines ◽  
Cross Coupling ◽  
Phenyl Boronic Acid

Nanoporous Cu2(BDC)2(BPY)–MOF was used as efficient and reusable heterogeneous catalyst to effect the aerobic cross-coupling of aromatic amines and phenyl boronic acid (Chan–Lam Coupling).

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