## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 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
Stereoselective synthesis of dialkyl 3-spiroindanedione-1,2,3,3a-tetrahydropyrrolo[1,2-a]quinoline-1,2-dicarboxylates
β Scribed by Issa Yavari; Anvar Mirzaei; Loghman Moradi; Nargess Hosseini
- Publisher
- Elsevier Science
- Year
- 2008
- Tongue
- French
- Weight
- 138 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
The 1:1 intermediate generated by the addition of quinoline to dialkyl acetylenedicarboxylates is trapped by 1,3-indanedione to yield dialkyl 3-spiroindanedione-1,2,3,3a-tetrahydropyrrolo[1,2-a]quinoline-1,2-dicarboxylates in good yields. The structures of these products were confirmed by NMR and single-crystal X-ray diffraction studies.
π SIMILAR VOLUMES
Alk&ractz 6h4ethoxy4methylquinoline was converted inlo 8-melhoxy-l,3,4,S-teuahydroFyrmlo[4,3,2~e]quinoline by a six reaction sequence in which the IWI wp wm the formation of ihe indole ring. damirone B ki i batielline C Cl Me isobatzellinr C dehydrobufotenino chloride
## Abstract For Abstract see ChemInform Abstract in Full Text.