Iodine monofluoride, generated from XeF 2 and I 2 or NIS, reacts with alkenes to furnish iodofluorinated products [cf. (II), (IV), (V)] in good yields. The reaction of aromatics with XeF 2 and I 2 or NIS proceeds as electrophilic aromatic iodination [β (VII), (IX)]. Iodine monofluoride (IF), generat
ChemInform Abstract: A Mild and Effective Iodination Method Using Iodine in the Presence of Bis-(trifluoroacetoxy)iodobenzene.
β Scribed by R. BENHIDA; P. BLANCHARD; J.-L. FOURREY
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 38 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
Abstract
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable via the βReferencesβ option.
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
A Simple and Convenient Method for the Deprotection of Tetrahydropyranyl Ether Using Iodine in Methanol. -Iodine in methanol selectively cleaves primary and secondary tetrahydropyranyl and 4,4'-dimethoxytrityl protecting groups. Other protecting groups (such as benzoyl, benzyl, tert-butyloxycarbony