articleTop 10% cited
A General, Efficient, and Inexpensive Catalyst System for the Coupling of Aryl Iodides and Thiols
Organic Letters · 2002 · Vol. 4(20) · pp. 3517–3520
Fuk Yee Kwong✉(Massachusetts Institute of Technology)Stephen L. Buchwald(Massachusetts Institute of Technology)
Abstract
An efficient copper-catalyzed carbon-sulfur bond formation reaction was developed. This method is particularly noteworthy given its experimental simplicity, high generality, and exceptional level of functional group toleration and the low cost of the catalyst system. [reaction: see text]
Sulfur-Based Synthesis TechniquesChemical Synthesis and ReactionsCatalytic Cross-Coupling ReactionsChemistryCatalysisArylSimplicityGeneralityCombinatorial chemistrySulfurFunctional groupCoupling reactionReaction conditions
MeSH terms
CatalysisChemistry, OrganicCopperIodidesSulfhydryl CompoundsMolecular Structure
Funding
- Pfizer
Citations
513
FWCI
6.12
field-weighted impact
References
48
Percentile
97%
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References
Copper-Catalyzed Coupling of Alkylamines and Aryl Iodides: An Efficient System Even in an Air Atmosphere
Organic Letters · 2002 · 503 citations
Formation of Aryl−Nitrogen, Aryl−Oxygen, and Aryl−Carbon Bonds Using Well-Defined Copper(I)-Based Catalysts
Organic Letters · 2001 · 542 citations
The Palladium Catalyzed Nucleophilic Substitution of Aryl Halides by Thiolate Anions
Bulletin of the Chemical Society of Japan · 1980 · 405 citations
An efficient copper-catalyzed coupling of aryl halides with imidazoles
Tetrahedron Letters · 1999 · 346 citations
Copper-Catalyzed Coupling of Aryl Iodides with Aliphatic Alcohols
Organic Letters · 2002 · 383 citations
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