Results 21 to 30 of about 47,675 (279)

Ruthenium-Catalyzed Cycloaddition of Alkynes and Organic Azides

open access: yes, 2016
Cp*RuCl(PPh3)2 is an effective catalyst for the regioselective “fusion” of organic azides and terminal alkynes, producing 1,5-disubstituted 1,2,3-triazoles.
Xinguo Chen (295183)   +7 more
core   +5 more sources

Electrochemical Hydroboration of Alkynes [PDF]

open access: yesChemistry – A European Journal, 2021
Abstract Herein we reported the electrochemical hydroboration of alkynes by using B 2 Pin 2 as the boron source. This unprecedented reaction manifold was applied to a broad range of alkynes, giving the hydroboration products in good to
Maude Aelterman   +3 more
openaire   +2 more sources

Iodine-mediated hydration of alkynes on keto-functionalized scaffolds: mechanistic insight and the regiospecific hydration of internal alkynes

open access: yesBeilstein Journal of Organic Chemistry, 2019
An iodine-mediated hydration reaction of alkynes serves as a green alternative to metal-catalyzed procedures. Previous work has shown that this method works well with terminal alkynes on keto-functionalized scaffolds, including 1,3-dicarbonyls and their ...
Zachary Lee   +8 more
doaj   +1 more source

Chemoselective Biohydrogenation of Alkenes in the Presence of Alkynes for the Homologation of 2‐Alkynals/3‐Alkyn‐2‐ones into 4‐Alkynals/Alkynols [PDF]

open access: yesAdvanced Synthesis & Catalysis, 2019
AbstractThe chemoselective hydrogenation of alkenes in the presence of alkynes is a very challenging transformation to achieve with traditional chemical methods. The development of an effective procedure to perform this transformation would enrich the tool‐kit available to organic chemists for the development of useful synthetic routes, and the ...
Colombo D.   +6 more
openaire   +3 more sources

From Amines to Alkynes – Lighting the Way [PDF]

open access: yes, 2018
We present a metal-free photoredox strategy for the formation of Csp3-Csp bonds from redox-activated primary amine derivatives. The developed reaction of 2,4,6-triphenylpyridiniu salts with alkynyl tosylates, leading to functionalized alkynes , is easily
Michał, Ociepa   +2 more
core   +1 more source

Recent Advances in the Addition of Amide/Sulfonamide Bonds to Alkynes

open access: yesMolecules, 2019
The addition of amide/sulfonamide bonds to alkynes is not only one of the most important strategies for the direct functionalization of carbon–carbon triple bonds, but also a powerful tool for the downstream transformations of amides/sulfonamides ...
Fei Zhao   +5 more
doaj   +1 more source

Efficient Sonogashira Coupling Reaction Catalyzed by Copper (I) Iodide in the Presence of KF/Al2O3 [PDF]

open access: yesشیمی کاربردی روز, 2009
We have developed a convenient and efficient method for coupling of aryl iodides and bromides with terminal alkynes. The protocol uses CuI as catalyst, 1, 10-phenanthroline as ligand, KF/Al2O3 as base and toluene as solvent.
Rahman Hosseinzadeh   +2 more
doaj   +1 more source

Reactions of Tetracyclone Molybdenum Complexes with Electrophilic Alkynes: Cyclopentadienone–Alkyne Coupling and Alkyne Coordination [PDF]

open access: yesOrganometallics, 2017
The reactions of the complexes [Mo(CO)2(η4-C4Ph4CO)2] and [Mo(CO)3(NCMe)(η4-C4Ph4CO)] with the alkynes dimethyl acetylenedicarboxylate (DMAD; RC≡CR where R = CO2Me) and methyl propiolate (RC≡CH) have been studied. In the case of DMAD, the initial product is the green carbonyl complex [Mo(CO)(RC≡CR)(η5,σ-C4Ph4COCR═CR)] (3), in which two alkyne molecules
Adams, H.   +4 more
openaire   +2 more sources

The Effect of N-Donor Ligands on the Reaction of Ruthenium Hydrides with 1-Alkynes

open access: yes, 2016
Neutral ruthenium hydrides Ru(CO)ClH(L)(PPh3)2 bearing one N-donor ligand react with 1-alkynes at 23 °C to yield neutral alkenyl complexes Ru(CO)Cl(CHCHR)(L)(PPh3)2.
Antonio M. Echavarren (1299936)   +5 more
core   +1 more source

Iron-catalyzed formation of six-membered rings from alkyne

open access: yesGreen Synthesis and Catalysis
Iron compounds, exhibiting high catalytic behavior and excellent compatibility, have been considered as low-toxic, cheap, efficient, and green catalysts for many important organic transformations.
Hui Li   +7 more
doaj   +1 more source

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