✍ Scribed by P. Sai Prathima; C. Uma Maheswari; K. Srinivas; M. Mohan Rao
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Aryl‐substituted olefins are prone to vicinal dioxygenation under conditions A) to give mono‐acetylated diols.
📜 SIMILAR VOLUMES
## Abstract A mild and efficient synthesis of the title compounds (III) via reaction of 4‐hydroxy‐6‐methyl‐pyran‐one with various substituted 2‐hydroxybenzaldehydes in water is described.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract The reaction works best with organic bromides: 1,3‐dipolar cycloaddition of the resulting alkyl‐ and aryl azides with terminal alkynes affords disubstituted 1,2,3‐triazoles regioselectively.