## 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 โFull Textโ option. The original article is trackable v
Studies on phosphonium ylides XXI. Reactions of Wittig reagents with substituted 2-amino-1,4-naphthoquinones
โ Scribed by Leila Sadek Boulos; Mona Hizkial Nasr Arsanious
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 412 KB
- Volume
- 53
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
โฆ Synopsis
The reaction of methoxycarbonylmethylene 2b-and ethoxycarbonylmethylene 2e-triphenylphosphoranes with substituted 2-amino-l,4naphthoquinones la-c afforded the new p>rroline-ylidphosphoranes 3b-3g via 1,2-and 1,4-addition reactions. On the other hand, 2-dimethylamino-l,4-naphthoquinone ld reacts with cyanomethylenetriphenylphosphorane 2d to give adduct 4. Mechanisms accounting for the formation of the new prevJucts are discussed.
๐ SIMILAR VOLUMES
## Abstract Wittig reagents (__1aโc__) react with Nโ(phenylsulfonyl)โ1,4โbenzoquinone monoimine __2a__ to give adducts __3a__, __4a__, and __4b__. On the other hand, the reactions of __2b__ with the same ylides (__1aโc__) yield the new products __3b__, __6a__, and __6b__, respectively. Mechanisms a
## 1, 3, 2, fide 1 reacts with substituted 2-amino-1,4-naphthoquinons 2a-d to give 4,5,4ะ,5ะ-benzodiphenoquinonebis-1,3,2-thiazaphospholine-2-sulfide derivatives of type 3. Compatible analytical and spectroscopic results were obtained for all the new compounds. A mechanism is proposed to explain t
4-(4-Methylphenyl)-2,3-benzoxazin-1-one (1) reacts thermally with a series of alkylidene phosphoranes and the relevant salts to give mainly substituted isoquinolines. Thus, compound 1 reacts with ester ylides 2a and 2b to give isoquinolones 7a and 7b, whereas with benzoylmethylenetriphenylphosphoran