Full article: Unusual synthesis of azines and their oxidative degradation to carboxylic acid using iodobenzene diacetate
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A one-pot oxidative decarboxylation–Friedel-Crafts reaction of acyclic α-amino acid derivatives activated by the combination of iodobenzene diacetate ... - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/B815227F
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Synthesis of α-sulfonyloxyketones via iodobenzene diacetate (PIDA)-mediated oxysulfonyloxylation of alkynes with sulfonic acids - RSC Advances (RSC Publishing) DOI:10.1039/C7RA11875A
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Recent Advances in Iodosobenzene‐Mediated Construction of Heterocyclic Scaffolds: Transition‐Metal‐Free Approaches and Scope - Gayen - 2018 - European Journal of Organic Chemistry - Wiley Online Library
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organic chemistry - Mechanism of oxidative dearomatisation with hypervalent iodine - Chemistry Stack Exchange
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A facile iodine(III)-mediated synthesis of 3-(3-aryl-1-phenyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[4,3-a]pyridines via oxidation of 2-((3-aryl-1-phenyl-1H-pyrazol-4-yl)methylene)-1-(pyridin-2-yl)hydrazines and their antimicrobial evaluations | Organic and ...
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Synthesis of α-sulfonyloxyketones via iodobenzene diacetate (PIDA)-mediated oxysulfonyloxylation of alkynes with sulfonic acids - RSC Advances (RSC Publishing) DOI:10.1039/C7RA11875A
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Iodine(III) promotes cross-dehydrogenative coupling of N-hydroxyphthalimide and unactivated C(sp3)–H bonds | Communications Chemistry
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Iodine(III) promotes cross-dehydrogenative coupling of N-hydroxyphthalimide and unactivated C(sp3)–H bonds | Communications Chemistry
![A one-pot oxidative decarboxylation–Friedel-Crafts reaction of acyclic α-amino acid derivatives activated by the combination of iodobenzene diacetate ... - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/B815227F A one-pot oxidative decarboxylation–Friedel-Crafts reaction of acyclic α-amino acid derivatives activated by the combination of iodobenzene diacetate ... - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/B815227F](https://pubs.rsc.org/image/article/2008/OB/b815227f/b815227f-s4.gif)