Results 21 to 30 of about 45,374 (213)

[3+2] Cycloaddition of alkyl aldehydes and alkynes enabled by photoinduced hydrogen atom transfer

open access: yesNature Communications, 2022
In contrast to the prevalence of 1,3-dipolar cycloadditions, radical [3+2] annulations of alkynes are underexplored. Here, the authors describe [3+2] cycloadditions of various internal alkynes with readily accessible aliphatic aldehydes via photoinduced ...
Siya Le   +6 more
doaj   +1 more source

Synthesis of aryl-1H-1,2,3-triazoles via 1,3-dipolar cycloaddition

open access: yesOrbital: The Electronic Journal of Chemistry, 2012
A series of Aryl-1H-1,2,3-triazoles were prepared from the reaction between aril-azide (1) with 1.5 equiv. of terminal alkynes (2a-o). The reactions carried out at room temperature and in the presence of CuI (10 mol%) in acetonitrile. The compounds (3a-o)
Wagner O. Valença   +2 more
doaj   +1 more source

Selective Manganese-Catalyzed Dimerization and Cross-Coupling of Terminal Alkynes [PDF]

open access: yes, 2021
For the first time, an efficient manganese-catalyzed dimerization of terminal alkynes to afford 1,3-enynes is described. This reaction is atom economic, implementing an inexpensive, earth abundant non-precious metal catalyst.
Karl, Kirchner   +5 more
core   +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

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

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

Selective C-H Halogenation of Alkenes and Alkynes Using Flavin-Dependent Halogenases [PDF]

open access: yes, 2023
Single component flavin-dependent halogenases (FDHs) possesses both flavin reductase and FDH activity in a single enzyme. We recently reported that the single component FDH AetF catalyzes site-selective bromination and iodination of a variety of aromatic
Cahmlo, Olive   +3 more
core   +2 more sources

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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