Articles written in Journal of Chemical Sciences
Volume 121 Issue 6 November 2009 pp 1035-1040
Highly functionalized (𝐸)-2-arylvinyl bromides were prepared in high yields through a new convenient access by acylation of (𝐸)-4-(2-bromovinyl)phenol with fatty and aromatic acids at room temperature using dicyclohexyl carbodiimide (DCC) and dimethylaminopyridine (DMAP).
Volume 129 Issue 3 March 2017 pp 289-294 Rapid Communication
CuI-catalyzed selective Ullmann C–O coupling of 1,4-disubstituted 1,2,3-triazole bromides with phenols were achieved through the coordination of N(2) atom. The ortho C–Br bond in N(1) aryl can be selectively coupled with phenols, while other C–Br bonds remain inert, generating ortho aryloxyl 1,4-diaryl1,2,3-triazoles.
Volume 131 Issue 7 July 2019 Article ID 0055
A facile and efficient method for direct C–H formylation of phenolated 1,4-disubstituted 1,2,3-triazoles using DMSO as the formyl source has been developed. The reaction proceeded smoothly under metal-free conditions with good functional group tolerance and high selectivity co-controlled by the triazole ring and hydroxyl group.
Volume 134, 2022
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