|Related Categories||Alkynes, Building Blocks, Chemical Synthesis, Organic Building Blocks, Terminal More...|
|bp||87-91 °C/11 mmHg(lit.)|
|density||1.019 g/mL at 25 °C(lit.)|
1,3-dipolar cycloaddition of acceptor-cyclopropylmethy
Forms the corresponding propargyl aldehyde in good yield directly from DMF-dimethyl acetal without the need for making an acetylide salt.
Used together with an arylboronic acid and sodium azide in a copper-catalyzed, three-component synthesis of trisubstituted 1,2,4-triazoles. Employed in a study of a gold (III)-catalyzed hydroamination of alkynes leading to N-vinylindoles.
1, 5 g in glass bottle
Certificate of Analysis
Aldrich Chemistry lists over 600 alkyne building blocks, including a wide array of propargyl alcohols, acetylenic boron reagents, and halogenated substrates for cross-coupling. Additionally, many of ...
Keywords: Building blocks, Coupling reactions, Cross couplings
Tetrahedron Lett. 45, 5043, (2004)
Synlett, 278, (2007)
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