alkyne

(redirected from Alkynes)
Also found in: Dictionary, Medical, Encyclopedia.
Graphic Thesaurus  🔍
Display ON
Animation ON
Legend
Synonym
Antonym
Related
  • noun

Synonyms for alkyne

a colorless flammable gas used chiefly in welding and in organic synthesis

References in periodicals archive ?
1] disappeared, which corresponds to the stretching vibration of azide and alkyne C-H, respectively.
In 1978, we discovered Zr-catalyzed methylalumination of alkynes (ZMA) (19)-(21) and tentatively proposed its mechanism as shown in Scheme 1.
Alkynes are known to participate in so-called 'click chemistry' reactions making it simple and easy to add other molecular layers above the first.
Recently, the Huisgen 1,3 dipolar cycloaddition of azides to alkynes to yield 1,2,3 triazoles has emerged as a highly useful and premier example of click chemistry [10-15].
Cycloaddition of thiophene S-oxides to allenes, alkynes and to benzyne, New Journal of Chemistry, 27: 1377-1384.
The IR findings revealed involvement of carboxyl (-COOH), hydroxyl (-OH), amides (-NH), amine (-NH), alkynes (CH), alkanes (CH2, CH3), ethers (C-O), ketones (C=O) and some other miscellaneous groups i.
In this way the 1,2,4-triazines can be reacted with alkynes to form pyridine rings.
1] can be assigned to alkynes carbon triple bond stretching vibration, with possible contribution from C=C=C bond stretching vibration of allenes [13].
alkanes, naphthenes, alkynes, aromatics, and others), from viscously
According to the editors (both of the National Center for Scientific Research, France), the selective activations of terminal alkynes and propargylic alcohols via vinylidene- and allenylidene-metal intermediates play an important role in recent developments of synthetic methods with useful applications in the synthesis of natural products and molecular materials and have opened new catalytic routs toward anti-Markovnikov additions to terminal alkynes, carbocyclizations, or propargylations.
The BRI system has unique balled media and can also effectively biodegrade various alkynes, alkenes, and many aromatic compounds, according to Boswell.
Furthermore, for reduction, gold can hydrogenate alkenes, alkynes, imines and carbonyls in the presence of H2.