Efficient Cu-catalyzed one-pot odorless synthesis of sulfides from triphenyltin chloride, aryl halides and S 8 in PEG-Reference-Cited by-同舟云学术

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Efficient Cu-catalyzed one-pot odorless synthesis of sulfides from triphenyltin chloride, aryl halides and S 8 in PEG

Published:2016-01 Issue:2 Volume:57 Page:192-195
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Rostami Abed,Rostami Amin,Iranpoor Nasser,Zolfigol Mohammad Ali

Funder

Iran National Science Foundation

University of Kurdistan Research Councils

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference62 articles.

1. Diaryl sulfide-based inhibitors of trypanothione reductase: inhibition potency, revised binding mode and antiprotozoal activities

2. Investigations on the 4-Quinolone-3-carboxylic Acid Motif. 1. Synthesis and Structure−Activity Relationship of a Class of Human Immunodeficiency Virus type 1 Integrase Inhibitors

3. Novel p-Arylthio Cinnamides as Antagonists of Leukocyte Function-Associated Antigen-1/Intracellular Adhesion Molecule-1 Interaction. 2. Mechanism of Inhibition and Structure-Based Improvement of Pharmaceutical Properties

4. The Palladium Catalyzed Nucleophilic Substitution of Aryl Halides by Thiolate Anions

5. A general and efficient method for the palladium-catalyzed cross-coupling of thiols and secondary phosphines

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2. Research Progress in C—S Coupling Reactions of Aryl Halides;Chinese Journal of Organic Chemistry;2023

3. 15-Membered Macrocyclic Schiff-Base-Pd(0) Complex Immobilized on Fe3O4 MNPs: An Novel Nanomagnetic Catalyst for the One-Pot Three-Component C–H Chalcogenation of Azoles by S8 and Aryl Iodides;Catalysis Letters;2022-10-26

4. Transition-Metal-Catalyzed C–S, C–Se, and C–Te Bond Formations via Cross-Coupling and Atom-Economic Addition Reactions. Achievements and Challenges;Chemical Reviews;2022-09-16

5. Transition-metal-catalyzed one-pot selenylation of electrophilic arylating agents using triphenyltin chloride/Se as a phenylselenating agent;Organic & Biomolecular Chemistry;2022

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