Hypervalent Iodine Reagents for the Oxidation of Alcohols and Their Application to Complex Molecule Synthesis
✍ Scribed by Hirofumi Tohma; Yasuyuki Kita
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 424 KB
- Volume
- 346
- Category
- Article
- ISSN
- 1615-4150
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✦ Synopsis
Abstract
Hypervalent iodine(V) derivatives such as 2‐iodoxybenzoic acid (IBX) and Dess–Martin periodinane [DMP; 1,1,1‐tris(acetyloxy)‐1,1‐dihydro‐1,2‐benziodoxol‐3‐(1__H__)‐one] have been used widely for the oxidation of alcohols to aldehydes and ketones during the last decade because of their high chemoselectivity, mild reactivity, and high yielding process. This review focuses on the recent progress in the oxidation of alcohols to carbonyl compounds using IBX, DMP, and other hypervalent iodine reagents, and their application to total syntheses of a variety of complex natural products.
📜 SIMILAR VOLUMES
## Abstract The domino reaction of 2,3‐epoxy‐1‐alcohol derivatives, namely tetrasubstituted 2,3‐epoxy‐1‐alcohols and 2‐ or 3‐alkyl trisubstituted 2,3‐epoxy‐1‐alcohols, with PhI(OCOCF~3~)~2~ in the presence of H~2~O is described in detail. In this reaction, several types of lactol derivatives can be
Hypervalent Iodine in Synthesis. Part 24. A Facile Method for the Preparation of Arylsulfinic Esters: Oxidation of Disulfides or Thiophenols by Phenyliodine(III) Bis(trifluoroacetate) in the Presence of Alcohols. -The oxidative reaction of disulfides (I) and thiophenols (IV) occurs readily in a sin