ChemInform Abstract: Cyclic Dimerization of 2-Piperidylglycine.
โ Scribed by K. CHUNG; D. LEE; H. KIM
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 29 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
โฆ Synopsis
Cyclic Dimerization of 2-Piperidylglycine.
-As part of studies on the preparation of the antitumor agent DKP 593A a good method for preparing the piperazine-2,5-dione (VIII) from 2-piperidylglycine derivative (I) is found. If the intermediate (VI) is protected by Cbz instead of Boc the corresponding piperazinedione is not formed. -(CHUNG, K.; LEE, D.; KIM, H.; Bull.
๐ SIMILAR VOLUMES
Spontaneous Dimerization of 2-(4-Methylphenylamino)thiophene. -The new title thiophene (III), prepared from thiophenethiole (I) and ptoluidine (II), undergoes spontaneously a dimerization during storage at room temperature to produce the compound (IV). -(VVEDENSKII, V.