2010
DOI: 10.1016/j.tet.2009.12.046
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Hypervalent iodine-mediated phenol dearomatization in natural product synthesis

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Cited by 606 publications
(172 citation statements)
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References 240 publications
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“…[47] Other common transformations mediated by hypervalent iodine include oxidative aryl coupling reactions, dehydrogenation of ketones, aziridination, epoxidation, rearrangements, fragmentations, and deprotection of dithianes.…”
Section: Organic Synthesismentioning
confidence: 99%
“…[47] Other common transformations mediated by hypervalent iodine include oxidative aryl coupling reactions, dehydrogenation of ketones, aziridination, epoxidation, rearrangements, fragmentations, and deprotection of dithianes.…”
Section: Organic Synthesismentioning
confidence: 99%
“…[47] Andere typischerweise von hypervalentem Iod vermittelte Reaktionen umfassen oxidative Arylkupplungen, Dehydrierung von Ketonen, Aziridinierung, Epoxidierung, Umlagerungen, Fragmentierungen und Entschützen von Dithianen.…”
Section: Aufsätzeunclassified
“…[12] Using this methodology, intramolecular oxidation of O-silylated phenols bearing various types of aminoquinones at the para position gave azacarbocyclic spiro dienones in good yields (Scheme 87). [170] This reaction was applied in the total synthesis of discorhabdin C. A certain type of iodonium ylides, called iodonium bis(sulfonyl)methylides, react with enones in a [3+2] cycloaddition catalyzed by rhodium(II) acetate, delivering arylindanes in moderate yields (Scheme 88).…”
Section: Aminohalogenationmentioning
confidence: 99%
“…Oxidative dearomatization of phenols, which can be considered as a special type of α-functionalization, has recently been reviewed and is therefore omitted. [12] 2 Oxygenation…”
Section: Introductionmentioning
confidence: 99%