Reaction of anthranil with N-phenylmaleimide
✍ Scribed by Taylor, Edward Curtis; Eckroth, David R.; Bartulin, Juan
- Book ID
- 125930571
- Publisher
- American Chemical Society
- Year
- 1967
- Tongue
- English
- Weight
- 250 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract The triethylamine‐catalyzed reactions of methyl __N__‐(cyanothioformyl)anthranilate (**1**) with isocyanates result in cyclization involving the cyano group to form methyl 2‐(4‐imino‐2‐oxo‐3‐substituted‐5‐thioxoimi‐dazolidin‐1‐yl)benzoates (**4**). Ring closure at the ester carbonyl to
Dan8 le cadre de travaux consacrhs % I'Ctudedes reactions des diazoalcanes 1\*2\*3 nous envisageons 1'6tudcde lareaction des aryldiasomCthanes substitues avec la N-ph~nylmalCimide. L%tude de la &action de certain6 diazoalcanes sur la N-phCnylmal6imide et ses dCri-&s a dkj% e'tk entreprise par d'autr
## 2,4,6-Trialkylphenylphospholes 3a (RסMe), 3b (Rסi-Pr) and 3c (Rסt-Bu), with increasing flattening at phosphorus and hence with increasing electron delocalisation, underwent the Diels-Alder reaction with N-phenylmaleimide to give predominantly cycloadducts 4a-c with the trialkylphenyl subs