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Srogl, Jiri, Liu, Wansheng, Marshall, Daniel, Liebeskind, Lanny S. (1999) Bio-organometallic Organosulfur Chemistry. Transi- tion Metal-Catalyzed Cross-Coupling Using Coen- zyme M or Thioglycolic Acid as the Leaving Group. Journal Of The American Chemical Society, 121 (40) 9449-9450 doi:10.1021/ja991654e

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Reference TypeJournal (article/letter/editorial)
TitleBio-organometallic Organosulfur Chemistry. Transi- tion Metal-Catalyzed Cross-Coupling Using Coen- zyme M or Thioglycolic Acid as the Leaving Group
JournalJournal Of The American Chemical Society
AuthorsSrogl, JiriAuthor
Liu, WanshengAuthor
Marshall, DanielAuthor
Liebeskind, Lanny S.Author
Year1999 (October)Volume121
Issue40
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/ja991654eSearch in ResearchGate
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Mindat Ref. ID1551024Long-form Identifiermindat:1:5:1551024:0
GUID0
Full ReferenceSrogl, Jiri, Liu, Wansheng, Marshall, Daniel, Liebeskind, Lanny S. (1999) Bio-organometallic Organosulfur Chemistry. Transi- tion Metal-Catalyzed Cross-Coupling Using Coen- zyme M or Thioglycolic Acid as the Leaving Group. Journal Of The American Chemical Society, 121 (40) 9449-9450 doi:10.1021/ja991654e
Plain TextSrogl, Jiri, Liu, Wansheng, Marshall, Daniel, Liebeskind, Lanny S. (1999) Bio-organometallic Organosulfur Chemistry. Transi- tion Metal-Catalyzed Cross-Coupling Using Coen- zyme M or Thioglycolic Acid as the Leaving Group. Journal Of The American Chemical Society, 121 (40) 9449-9450 doi:10.1021/ja991654e
In(1999, October) Journal Of The American Chemical Society Vol. 121 (40) American Chemical Society (ACS)

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Liebeskind, Lanny S., Srogl, Jiri (2002) Heteroaromatic Thioether−Boronic Acid Cross-Coupling under Neutral Reaction Conditions. Organic Letters, 4. 979-981 doi:10.1021/ol0200091
Liebeskind, Lanny S., Srogl, Jiri (2000) Thiol Ester−Boronic Acid Coupling. A Mechanistically Unprecedented and General Ketone Synthesis. Journal Of The American Chemical Society, 122 (45) 11260-11261 doi:10.1021/ja005613q
Villalobos, Janette M., Srogl, Jiri, Liebeskind, Lanny S. (2007) A New Paradigm for Carbon−Carbon Bond Formation:  Aerobic, Copper-Templated Cross-Coupling. Journal Of The American Chemical Society, 129 (51) 15734-15735 doi:10.1021/ja074931n
Savarin, Cecile, Srogl, Jiri, Liebeskind, Lanny S. (2000) Thiol Ester−Boronic Acid Cross-Coupling. Catalysis Using Alkylative Activation of the Palladium Thiolate Intermediate. Organic Letters, 2. 3229-3231 doi:10.1021/ol000231a
Savarin, Cecile, Srogl, Jiri, Liebeskind, Lanny S. (2001) Substituted Alkyne Synthesis under Nonbasic Conditions:  Copper Carboxylate-Mediated, Palladium-Catalyzed Thioalkyne−Boronic Acid Cross-Coupling. Organic Letters, 3. 91-93 doi:10.1021/ol006807d
Srogl, Jiri, Allred, Gary D., Liebeskind, Lanny S. (1997) Sulfonium Salts. Participantspar Excellencein Metal-Catalyzed Carbon−Carbon Bond-Forming Reactions. Journal Of The American Chemical Society, 119 (50) 12376-12377 doi:10.1021/ja9726926
Liebeskind, Lanny S., Srogl, Jiri, Savarin, Cecile, Polanco, Concepcion (2002) Bioinspired organometallic chemistry. Pure and Applied Chemistry, 74 (1) 115-122 doi:10.1351/pac200274010115
Savarin, Cecile, Srogl, Jiri, Liebeskind, Lanny S. (2002) A Mild, Nonbasic Synthesis of Thioethers. The Copper-Catalyzed Coupling of Boronic Acids withN-Thio(alkyl, aryl, heteroaryl)imides. Organic Letters, 4. 4309-4312 doi:10.1021/ol026948a
Wittenberg, Rüdiger, Srogl, Jiri, Egi, Masahiro, Liebeskind, Lanny S. (2003) Ketone Synthesis under Neutral Conditions. Cu(I) Diphenylphosphinate-Mediated, Palladium-Catalyzed Coupling of Thiol Esters and Organostannanes. Organic Letters, 5. 3033-3035 doi:10.1021/ol034962x
Kusturin, Carrie, Liebeskind, Lanny S., Rahman, Hayat, Sample, Kirby, Schweitzer, Barbara, Srogl, Jiri, Neumann, William L. (2003) Switchable Catalysis:  Modular Synthesis of Functionalized Pyrimidinones via Selective Sulfide and Halide Cross-Coupling Chemistry. Organic Letters, 5. 4349-4352 doi:10.1021/ol035649y
Allred, Gary D., Liebeskind, Lanny S. (1996) Copper-Mediated Cross-Coupling of Organostannanes with Organic Iodides at or below Room Temperature. Journal Of The American Chemical Society, 118 (11) 2748-2749 doi:10.1021/ja9541239
 
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