𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Quinazolines. I. Oxidation of indole-1,2-dicarboximides and subsequent conversion of their oxidation products to quinazolinones

✍ Scribed by Ishizumi, Kikuo; Inaba, Shigeho; Yamamoto, Hisao

Book ID
121448492
Publisher
American Chemical Society
Year
1973
Tongue
English
Weight
445 KB
Volume
38
Category
Article
ISSN
0022-3263

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Synthesis of oximes, conversion to nitri
Synthesis of oximes, conversion to nitrile oxides and their subsequent 1,3-dipolar cycloaddition reactions under microwave irradiation and solvent-free reaction conditions
✍ BΓ©atrice Touaux; FranΓ§oise Texier-Boullet; Jack Hamelin πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 147 KB πŸ‘ 2 views

Aldoximes and ketoximes were readily synthesized from aldehydes and hydroxylamine hydrochloride on Al 2 O 3 without solvent under microwave irradiation. At higher irradiation power, aldoximes dehydrated to nitriles and ketoximes rearranged to amides. Aldoximes reacted in a one-pot reaction with Nchl

ChemInform Abstract: Synthesis of Oximes
ChemInform Abstract: Synthesis of Oximes, Conversion to Nitrile Oxides and Their Subsequent 1,3-Dipolar Cycloaddition Reactions under Microwave Irradiation and Solvent-Free Reaction Conditions.
✍ B. TOUAUX; F. TEXIER-BOULLET; J. HAMELIN πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 34 KB πŸ‘ 1 views

Synthesis of Oximes, Conversion to Nitrile Oxides and Their Subsequent 1,3-Dipolar Cycloaddition Reactions under Microwave Irradiation and Solvent-Free Reaction Conditions. -Aldoximes and ketoximes (II) are readily synthesized from aldehydes and ketones (I) on Al 2 O 3 under microwave irradiation.