2016
DOI: 10.1007/s11172-016-1301-7
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Synthesis of (α-nitroalkyl-ONN-azoxy)furoxan derivatives

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Cited by 5 publications
(1 citation statement)
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“…The isolated yields for these products was low (5-9% yield), whilst side reaction products 3,3-dimethyl-4,4-azoxyfuroxans 5 were formed in higher yields (up to 28%). [16] In 2017, Li and co-workers described a silver catalysed Hunsdiecker bromination on a broad range of carboxylic acids 6 yielding alkyl and benzyl bromides 7 (Scheme 4). [17] After identifying some underlying issues with other catalytic protocols in the field (expensive metals, instability of products using alternative methods), the group discovered a silver-catalyzed radical process (2.5 mol% of Ag(Phen) 2 OTf was optimum using mild conditions) with dibromoisocyanuric acid as the best brominating source (when NBS was utilized, no reaction occurred, and only trace amounts of product formed when employing DBH).…”
Section: Dibromoisocyanuric Acid: Applications In Organic Reactions 2mentioning
confidence: 99%
“…The isolated yields for these products was low (5-9% yield), whilst side reaction products 3,3-dimethyl-4,4-azoxyfuroxans 5 were formed in higher yields (up to 28%). [16] In 2017, Li and co-workers described a silver catalysed Hunsdiecker bromination on a broad range of carboxylic acids 6 yielding alkyl and benzyl bromides 7 (Scheme 4). [17] After identifying some underlying issues with other catalytic protocols in the field (expensive metals, instability of products using alternative methods), the group discovered a silver-catalyzed radical process (2.5 mol% of Ag(Phen) 2 OTf was optimum using mild conditions) with dibromoisocyanuric acid as the best brominating source (when NBS was utilized, no reaction occurred, and only trace amounts of product formed when employing DBH).…”
Section: Dibromoisocyanuric Acid: Applications In Organic Reactions 2mentioning
confidence: 99%