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Advanced Synthesis & Catalysis, ISSN 1615-4150, 06/2014, Volume 356, Issue 9, pp. 2029 - 2039
A highly efficient and mild palladium‐catalyzed cross‐coupling of sodium sulfinates and alkynes for the selective synthesis of unsymmetrical internal alkynes and vinyl sulfones has been developed... 
palladium catalyst | cross‐coupling | alkynes | sodium sulfinates | vinyl sulfones | cross-coupling | OXIDATION | CARBON | ONE-POT SYNTHESIS | SULFIDES | CHEMISTRY, ORGANIC | DIARYL SULFONES | ARYL HALIDES | SONOGASHIRA REACTION | HYDROGEN-PEROXIDE | BOND ACTIVATION | CHEMISTRY, APPLIED | CARBOXYLIC-ACIDS | Palladium catalysts | Palladium | Organosulfur compounds | Synthesis | Sodium | Accessibility | Tolerances | Catalysis | Sulfones | Functional groups | Alkynes
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 7/2011, Volume 108, Issue 28, pp. 11344 - 11349
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 09/2014, Volume 53, Issue 39, pp. 10457 - 10461
gem‐Difluoropropargyl bromides are versatile intermediates in organic synthesis, but have rarely been employed in transition‐metal‐catalyzed cross‐coupling reactions... 
difluoropropargyl bromides | palladium | organoboron reagents | cross‐coupling | fluorine | Palladium | Cross-coupling | Difluoropropargyl bromides | Fluorine | Organoboron reagents | SUBSTITUTION | ACTIVATION | ANALOGS | STABILIZATION | REGIOSELECTIVITY | FREE CLICK CHEMISTRY | REDUCTIVE ELIMINATION | CHEMISTRY, MULTIDISCIPLINARY | cross-coupling | BROMIDE | DERIVATIVES | EFFICIENT | Drugs | Boron | Synthesis | Aromatic compounds | Bromides | Compatibility | Fluorination | Alkynes
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 10/2015, Volume 54, Issue 44, pp. 12923 - 12927
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 02/2014, Volume 20, Issue 9, pp. 2605 - 2612
...‐pot multicomponent coupling approach with cleavage of the C(sp3)N bonds. Three or four components of aryl iodides, alkynes, and amines were involved in this coupling process... 
multicomponent reactions | palladium | indoles | cleavage reactions | synthetic methods | Amines - chemistry | Phosphines - chemistry | Heterocyclic Compounds - chemistry | Indoles - chemical synthesis | Ligands | Alkynes - chemistry | Iodides - chemistry | Molecular Structure | Catalysis | Indoles - chemistry | Palladium - chemistry | Synthesis | Amines | Iodides | Aromatic compounds | Joining | Indoles | Derivatives | Alkynes
Journal Article
Chemical Society reviews, ISSN 0306-0012, 03/2014, Volume 43, Issue 5, pp. 1575 - 1600
Transition-metal (TM)-catalyzed hydroarylation reactions of alkynes have received much attention, because they enable the net insertion of alkyne C-C triple bonds into C-H bonds of aromatic precursors, resulting in regio... 
Transition Elements - chemistry | Heterocyclic Compounds - chemistry | Heterocyclic Compounds - chemical synthesis | Alkynes - chemistry | Boronic Acids - chemistry | Catalysis | Palladium - chemistry
Journal Article