The structures of 2,2-dialkyl-1,3,2-dithiastannolanes
✍ Scribed by Alwyn G. Davies; Seán D. Slater; David C. Povey; Gallienus W. Smith
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- English
- Weight
- 751 KB
- Volume
- 352
- Category
- Article
- ISSN
- 0022-328X
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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 si
**Azimines VI: 1‐Alkoxycarbonyl‐2,3‐dialkyl‐ and ‐2,3‐diarylazimines** Alkoxycarbonyl‐nitrenes **2** – generated in situ by α‐elimination from __N__‐[(4‐nitrophenyl)‐sulfonyloxy]carbamates **4** – were reacted with six aliphatic and aromatic azo compounds to yield 1‐alkoxycarbonyl‐azimines **11** (