An efficient combination of Dess-Martin periodinane with molecular iodine and KBr for the facile oxidative aromatization of Hantzsch 1,4-dihydropyridines

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The crystal structure of the Dess–Martin periodinane

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Oxidative cleavage of vicinal diols: IBX can do what Dess-Martin periodinane (DMP) can.

The fact that IBX exhibits reactivity akin to DMP is demonstrated from the results observed with strained and sterically hindered syn 1,2-diols, which undergo oxidative cleavage via a 12-I-5 spirobicyclic periodinane. The use of TFA, a protonating solvent, promotes the formation of the 12-I-5 intermediate for 1,2-diols of all types (sec,sec, sec,tert and tert,tert), leading to efficient oxidati...

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Iodine(V) reagents in organic synthesis. Part 2. Access to complex molecular architectures via Dess-Martin periodinane-generated o-imidoquinones.

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ژورنال

عنوان ژورنال: Arkivoc

سال: 2008

ISSN: 1551-7012

DOI: 10.3998/ark.5550190.0009.c02