A General, Efficient, and Inexpensive Catalyst System for the Coupling of Aryl Iodides and Thiols

Fuk Yee Kwong; Stephen L. Buchwald

doi:10.1021/ol0266673

journal article Sep 11, 2002

A General, Efficient, and Inexpensive Catalyst System for the Coupling of Aryl Iodides and Thiols

Fuk Yee Kwong Stephen L. Buchwald

Organic Letters Vol. 4 No. 20 pp. 3517-3520 · American Chemical Society (ACS)

View at Publisher Save 10.1021/ol0266673

Topics

No keywords indexed for this article. Browse by subject →

References

50

[1]

For (2002)

[2]

Klapars A. J. Am. Chem. Soc. (2002) 10.1021/ja0260465

[3]

Klapars A. J. Am. Chem. Soc. (2001) 10.1021/ja016226z

[4]

Kwong F. Y. Org. Lett. (2002) 10.1021/ol0171867

[5]

Wolter M. Org. Lett. (2002) 10.1021/ol025548k

[6]

Wolter M. Org. Lett. (2001) 10.1021/ol0168216

[7]

Kiyomori A. Tetrahedron Lett. (1999) 10.1016/s0040-4039(99)00291-9

[8]

Marcoux J.-F. J. Am. Chem. Soc. (1997) 10.1021/ja971901j

[9]

Antilla J. C. Org. Lett. (2001) 10.1021/ol0160396

[10]

Gujadhur R. Tetrahedron Lett. (2001) 10.1016/s0040-4039(01)00888-7

[11]

Gujadhur R. K. Org. Lett. (2001) 10.1021/ol0170105

[12]

Kang S.-K. Synlett (2002) 10.1055/s-2002-20457

[13]

Fagan P. J. J. Am. Chem. Soc. (2000) 10.1021/ja000094c

[14]

Goodbrand H. B. J. Org. Chem. (1999) 10.1021/jo981804o

[15]

Buck E. J. Org. Lett. (2002) 10.1021/ol025839t

[16]

Liu G. J. Med. Chem. (2000) 10.1021/jm0002782

[17]

Beard R. L. J. Med. Chem. (1996) 10.1021/jm960386h

[18]

Nagai Y. J. Med. Chem. (1982) 10.1021/jm00351a012

[19]

Wang Y. Bioorg. Med. Chem. Lett. (2001) 10.1016/s0960-894x(01)00100-7

[20]

Bonnet B. Bioorg. Med. Chem. (2000) 10.1016/s0968-0896(99)00268-0

[21]

Sawyer J. S. J. Org. Chem. (1998) 10.1021/jo980800g

[22]

Kondo T. Chem. Rev. (2000) 10.1021/cr9902749

[23]

Using O Tetrahedron Lett. (1998) 10.1016/s0040-4039(97)10624-4

[24]

Using Collect. Czech. Chem. Commun. (1989) 10.1135/cccc19892240

[25]

J. Aust. J. Chem. (1985) 10.1071/ch9850899

[26]

Kalinin A. V. J. Org. Chem. (1999) 10.1021/jo990114x

[27]

Baxter A. J. G. J. Tetrahedron (1993) 10.1016/s0040-4020(01)91225-6

[28]

Rábai J. Synthesis (1990) 10.1055/s-1990-27033

[29]

Kulkarni N. N. Tetrahedron (1988) 10.1016/s0040-4020(01)86020-8

[30]

Dhareshwar G. P. Indian J. Chem. Sect. B. (1980)

[31]

Rajsner M. Collect. Czech. Chem. Commun. (1975) 10.1135/cccc19751604

[32]

Rajsner M. Collect. Czech. Chem. Commun. (1975) 10.1135/cccc19750719

[33]

Machek V. G. J. Prakt. Chem. (1942) 10.1002/prac.19421600105

[34]

Steinkopf W. Liebigs Ann. Chem. (1937) 10.1002/jlac.19375270117

[35]

Roberts K. C. J. Chem. Soc. (1929) 10.1039/jr9290000863

[36]

Migita T. Bull. Chem. Soc. Jpn. (1980) 10.1246/bcsj.53.1385

[37]

Kosugi M. Bull. Chem. Soc. Jpn. (1985) 10.1246/bcsj.58.3657

[38]

Zheng N. J. Org. Chem. (1998) 10.1021/jo9814703

[39]

McWilliams J. C. Org. Synth. (2002) 10.15227/orgsyn.079.0043

[40]

Li G. Y. Angew. Chem., Int. Ed. (2001) 10.1002/1521-3773(20010417)40:8<1513::aid-anie1513>3.0.co;2-c

[41]

Li G. Y. J. Org. Chem. (2001) 10.1021/jo010764c

[42]

Li G. Y. J. Org. Chem. (2002) 10.1021/jo010983y

[43]

Schopfer U. Tetrahedron (2001) 10.1016/s0040-4020(01)00157-0

[44]

Harr M. S. Synlett (1999) 10.1055/s-1999-2910

[45]

Ishiyama T. J. Organomet. Chem. (1996) 10.1016/s0022-328x(96)06495-9

[46]

Ciattini P. G. Tetrahedron Lett. (1995) 10.1016/0040-4039(95)00677-5

[47]

Ullmann Ber. Dtsch. Chem. Ges. (1903) 10.1002/cber.190303602174

[48]

Org. Lett. (2000) 10.1021/ol005832g

[49]

Palomo C. Tetrahedron Lett. (2000) 10.1016/s0040-4039(99)02269-8

[50]

The (2002)

Cited By

496

Ultrasound-Promoted C–S Cross-Coupling via the 1,4-Addition Reaction of Thiophenols with Quinonediimides

Xingxing Ji, Hongxue Zhang · 2026

The Journal of Organic Chemistry

Samarium Diiodide-Mediated Radical Thioetherification of Alkyl Bromides with Disulfide Ethers

Wei Zhou, Yongqi Liang · 2026

The Journal of Organic Chemistry

Visible-Light-Promoted C–S Cross-Coupling via Intermolecular Charge Transfer

Bin Liu, Chern-Hooi Lim · 2017

Journal of the American Chemical So...

Photoredox Mediated Nickel Catalyzed Cross-Coupling of Thiols With Aryl and Heteroaryl Iodides via Thiyl Radicals

Martins S. Oderinde, Mathieu Frenette · 2016

Journal of the American Chemical So...

Room‐Temperature Arylation of Thiols: Breakthrough with Aryl Chlorides

Min Jiang, Haifang Li · 2016

Angewandte Chemie International Edi...

Reaction under Ball-Milling: Solvent-, Ligand-, and Metal-Free Synthesis of Unsymmetrical Diaryl Chalcogenides

Nirmalya Mukherjee, Tanmay Chatterjee · 2013

The Journal of Organic Chemistry

Transition-Metal-Catalyzed C−S, C−Se, and C−Te Bond Formation via Cross-Coupling and Atom-Economic Addition Reactions

Irina P. Beletskaya, Valentine P. Ananikov · 2011

Chemical Reviews

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

Miki Murata, Stephen L. Buchwald · 2004

Tetrahedron

Metrics

496

Citations

50

References

Details

Published: Sep 11, 2002
Vol/Issue: 4(20)
Pages: 3517-3520

Authors

F

Fuk Yee Kwong

Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139

S

Stephen L. Buchwald

Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139

Cite This Article

Fuk Yee Kwong, Stephen L. Buchwald (2002). A General, Efficient, and Inexpensive Catalyst System for the Coupling of Aryl Iodides and Thiols. Organic Letters, 4(20), 3517-3520. https://doi.org/10.1021/ol0266673

A General, Efficient, and Inexpensive Catalyst System for the Coupling of Aryl Iodides and Thiols

You May Also Like