## 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 convenient synthesis of 1H-2,3-benzoxazines by an acid-catalyzed intramolecular Mitsunobu reaction
β Scribed by Hiroyuki Kai; Toru Nakai
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- French
- Weight
- 61 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
A convenient, efficient method for the preparation of benzoxazines is described. 2-(Hydroxyiminomethyl)benzyl alcohols were cyclodehydrated to construct 1H-2,3-benzoxazines by acid-catalyzed intramolecular Mitsunobu reaction. This reaction depended on the geometry of the hydroxyimino moiety in the reaction precursor.
π SIMILAR VOLUMES
A convenient procedure for preparation of the title compound of->99% ee starting from 1-(2,3-difluoro-6-nitrophenoxy)-2-propanone (3) is presented. The key reaction is the intramolecular cyclization reaction in the presence of zinc chloride.
A simple and efficient route to monoprotected E-and Z-2-alkylidene-1 ,Zpropanediols was developed. The key step involves an unusual regio-and stereoselective SR2' Mitsunobu reaction of substituted 3-hydtoxy-2methylenealkenoate. We recently reported that 3.4,~tri-0-benzyl-D-glucose could be used as a
## Abstract Cyclizations of substrates (I) and (III) under conditions A) gives the target benzoxazines.