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Hypervalent iodine oxidation: α-Functionalization of β-dicarbonyl compounds using iodosobenzene

✍ Scribed by Robert M. Moriarty; Radhe K. Vaid; Vasulinga T. Ravikumar; Beena K. Vaid; Thomas E. Hopkins


Publisher
Elsevier Science
Year
1988
Tongue
French
Weight
456 KB
Volume
44
Category
Article
ISSN
0040-4020

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📜 SIMILAR VOLUMES


Hypervalent iodine oxidation: Synthesis
✍ Robert M. Moriarty; Radhe K. Vaid; Thomas E. Hopkins; Beena K. Vaid; Atilla Tunc 📂 Article 📅 1989 🏛 Elsevier Science 🌐 French ⚖ 254 KB

Hypervalent iodine oxidation of Z-(trimethylsilyloxy)furan with iodosobenzeneboron bifluoride etherate in the presence of various nucleophiles yields 5-substituted-2(.5H)-furanones. 5Substituted-2(5H)-furanones are versatile intermediates for the synthesis of a number of important natural products a

Hypervalent iodine oxidation of amines u
✍ Robert M Moriarty; Radhe K Vaid; Michael P Duncan; Masahito Ochiai; Minako Inena 📂 Article 📅 1988 🏛 Elsevier Science 🌐 French ⚖ 256 KB

Primary aliphatic amines on oxidation with iodosobenzene in CH2C12 or H20 yield the corresponding nitriles, while primary cycloalkylamines give the corresponding cyclic ketones. Lactams are obtained by the oxidation of cyclic amines. (S)(-) Nicotine (JJ,) is oxidized to (+)-cotinine (a). The interm