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Synlett, ISSN 0936-5214, 10/2017, Volume 29, Issue 6, pp. 727 - 730
.... This trend is the same as that in the vinylidene rearrangement of internal alkynes at a group 8 metal center. 
cluster | reaction mechanism | internal alkyne | rearrangement | Physical Sciences | Chemistry | Chemistry, Organic | Science & Technology
Journal Article
Advanced synthesis & catalysis, ISSN 1615-4150, 08/2017, Volume 359, Issue 16, pp. 2847 - 2856
The stereoselective E‐iodosulfonylation of internal alkynes for synthesizing highly defined tetrasubstituted olefins using sodium phenyl sulfinate and iodine has been achieved... 
iodosulfonylation | radical reaction | difunctionalization | internal alkynes | iodine | Nitriles | Olefins | Alkenes | Substrates | Iodine | Alkynes
Journal Article
Advanced synthesis & catalysis, ISSN 1615-4150, 06/2019, Volume 361, Issue 12, pp. 2855 - 2863
...)indole with internal alkynes. Excess amounts of silver acetate (5.0 equiv.) were found to be crucial for the efficient C2 naphthylation and C2 enol esterification of indoles... 
Rhodium | C−H Functionalization | Internal Alkynes | N-(2-Pyrimidyl)indole | Acetates | Indoles | Esterification | Alkynes
Journal Article
Advanced synthesis & catalysis, ISSN 1615-4150, 07/2018, Volume 360, Issue 13, pp. 2429 - 2434
...‐alkyne cycloaddition (RhAAC) under mild conditions is reported. This approach is water and air compatible and has a broad substrate scope, good functional group tolerance, high yields and excellent regioselectivities... 
regioselectivity | internal alkynylphosphonates | mild conditions | triazolyl-4-phosphonates | rhodium | Rhodium | Phosphonates | Substitutes | Carbohydrates | Cycloaddition | Synthesis | Regioselectivity | Functional groups | Substrates | Alkynes
Journal Article
Macromolecular chemistry and physics, ISSN 1022-1352, 09/2014, Volume 215, Issue 17, pp. 1603 - 1608
Journal Article
Macromolecular rapid communications., ISSN 1022-1336, 08/2012, Volume 33, Issue 16, pp. 1356 - 1361
Journal Article
Kinetics and catalysis, ISSN 1608-3210, 12/2016, Volume 57, Issue 6, pp. 853 - 858
.... 857–864. Catalytic Properties of Nanostructured Pd–Ag Catalysts in the Liquid-Phase Hydrogenation of Terminal and Internal Alkynes A. V . Rassolov a , P . V... 
selectivity | liquid-phase hydrogenation | Pd–Ag | internal alkynes | terminal alkynes | catalyst structure | Chemistry | nanoparticles | bimetallic catalysts | Physical Chemistry | diphenylacetylene | Catalysis | phenylacetylene | Physical Sciences | Chemistry, Physical | Science & Technology | Palladium catalysts | Palladium | Hydrogenation | Analysis
Journal Article
Kinetics and catalysis, ISSN 0023-1584, 9/2016, Volume 57, Issue 5, pp. 625 - 631
Pd–In/Al2O3 and Pd–In/MgAl2O4 catalysts prepared from dinuclear Pd–In acetate complexes were studied in the hydrogenation of alkyne compounds with different structures. The Pd... 
Chemistry | 1-phenyl-1-propyne | bimetallic catalysts | liquid-phase hydrogenation | Physical Chemistry | diphenylacetylene | internal alkynes | terminal alkynes | Catalysis | phenylacetylene | kinetics | mechanism | Physical Sciences | Chemistry, Physical | Science & Technology | Palladium catalysts | Thermodynamics | Palladium | Adsorption | Hydrogenation | Analysis
Journal Article
Kinetics and catalysis, ISSN 0023-1584, 9/2016, Volume 57, Issue 5, pp. 617 - 624
.... 621–628. Supported Catalysts Based on Pd–In Nanoparticles for the Liquid-Phase Hydrogenation of Terminal and Internal Alkynes: 1. Formation and Structure P. V. M... 
catalyst structure | Chemistry | nanoparticles | liquid-phase hydrogenation | bimetallic catalysts | Physical Chemistry | acetate complex | Pd–In | internal alkynes | electron microscopy | terminal alkynes | Catalysis | Physical Sciences | Chemistry, Physical | Science & Technology | Palladium catalysts | Nanoparticles | Palladium | Hydrogen | Hydrogenation
Journal Article
Synlett, ISSN 0936-5214, 08/2015, Volume 26, Issue 13, pp. 1885 - 1889
...–H activation of benzamidine and terminal alkynes has been developed. In this practical and high-yielding process, the C... 
letter | terminal alkynes | C-H activation | internal oxidant | C-C bond coupling
Journal Article
Polymer (Guilford), ISSN 0032-3861, 01/2017, Volume 109, pp. 1 - 12
...) or copper catalyzed azide-alkyne cycloadditions. Di(2-ethylhexyl) phthalate derivatives (DEHP-ether and DEHP-ester... 
Internal plasticizer | Huisgen azide-alkyne cycloaddition | Phthalate diester | Polymer Science | Physical Sciences | Science & Technology | Copper | Esters | Analysis
Journal Article
Kinetics and catalysis, ISSN 1608-3210, 08/2017, Volume 58, Issue 4, pp. 480 - 491
Journal Article
Chinese journal of chemistry, ISSN 1001-604X, 05/2014, Volume 32, Issue 5, pp. 387 - 390
A new cross‐coupling reaction of N‐benzylic sulfonamides with terminal alkynes for the synthesis of internal alkynes is reported... 
internal alkynes | alkynylation | cross‐coupling | carbon nucleophiles | benzylic amines | cross-coupling
Journal Article
Chemistry : a European journal, ISSN 0947-6539, 04/2012, Volume 18, Issue 14, pp. 4179 - 4184
Taking control of boron: A highly regio‐ and stereoselective copper‐catalyzed hydroboration of unsymmetrical internal alkynes has been developed... 
copper | internal alkynes | homogeneous catalysis | hydroboration | alkynes | Boron | Hydroboration | Catalysts | Hydrides | Catalysis | Copper | Alkynes
Journal Article