Ötvös, Sándor Balázs and Hatoss, Gábor and Georgiádes, Ádám and Kovács, Szabolcs and Mándity, István and Novák, Zoltán and Fülöp, Ferenc (2014) CONTINUOUS-FLOW AZIDE–ALKYNE CYCLOADDITIONS WITH AN EFFECTIVE BIMETALLIC CATALYST AND A SIMPLE SCAVENGER SYSTEM. RSC Advances. ISSN 2046-2069
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Abstract
A flow chemistry-based technique is presented herein for Cu(I)-catalyzed azide–alkyne cycloadditions with a copper on iron bimetallic system as the catalyst and iron powder as a readily available copper-scavenger. The method proved to be rapid and safe as compared with the conventional batch experiment; and by using an in-line copper scavenger, the level of copper impurities in the triazole products could readily be reduced to negligibly small amounts. The process was widely applicable, as not only terminal alkynes, but also various disubstituted acetylenes were nicely tolerated as dipolarophiles leading to useful 1,4,5-trisubstituted 1,2,3-triazoles.
Item Type: | Article |
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Subjects: | Q Science / természettudomány > QD Chemistry / kémia > QD04 Organic chemistry / szerves kémia |
Depositing User: | Dr. Zoltán Novák |
Date Deposited: | 11 Feb 2015 09:10 |
Last Modified: | 11 Feb 2015 09:10 |
URI: | http://real.mtak.hu/id/eprint/21505 |
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