2016
DOI: 10.1002/chin.201610198
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ChemInform Abstract: Linear and V‐Shaped Alkynyl‐1,3,5‐triazines.

Abstract: The title triazines are obtained by sequential substitution of the 2‐ and 4‐chloro groups of 2,4‐dichloro‐1,3,5‐triazines by regioselective Sonogashira coupling.

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Cited by 3 publications
(3 citation statements)
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“…Materials and Procedures. Employing standard Schlenk techniques, all reactions were performed under a dry nitrogen atmosphere using a method described in the literature: triazine with a methoxy group substituent 24 and triazine-conjugated alkyne ligands 38 were synthesized. The other reagents were obtained from commercial sources.…”
Section: ■ Experimental Sectionmentioning
confidence: 99%
“…Materials and Procedures. Employing standard Schlenk techniques, all reactions were performed under a dry nitrogen atmosphere using a method described in the literature: triazine with a methoxy group substituent 24 and triazine-conjugated alkyne ligands 38 were synthesized. The other reagents were obtained from commercial sources.…”
Section: ■ Experimental Sectionmentioning
confidence: 99%
“…58). 92 2,4-Dichloro-1,3,5-triazine derivatives were selected as starting reagents. Sequential substitution of chlorine atoms using the Sonogashira cross-coupling reaction resulted in desired symmetric or asymmetric products in good yields.…”
Section: Synthesis and Photophysical Properties Of Alkenyl-and Alkyny...mentioning
confidence: 99%
“…This disubstituted-triazine derivative can be used as an intermediate to synthesize porous adsorbent materials which an be used to remove special metal ions [8] or to capture special gases [9]. There are some related structures [10][11][12] in the structural database.…”
Section: Commentmentioning
confidence: 99%