**Halochromic Molecules. Spectrophotometric Investigation of the Acidobasic Behaviour of Substituted 6,6‐Diphenyl‐6__H__‐chromeno[4, 3‐__b__]indolizines and their Aza‐analogues** Substituted 6,6‐diphenyl‐6__H__‐chromeno[4,3‐__b__]indolizines form ring‐opened, intensely coloured (diphenyl)‐indolizin
✦ LIBER ✦
Halochrome Molekeln. 5. Mitteilung. Synthese substituierter 6H-Chromeno[4,3-b]indolizine und ihrer Aza-analogen
✍ Scribed by Sigmund Gunzenhauser; Heinz Balli
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- German
- Weight
- 451 KB
- Volume
- 68
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
Halochromic Molecules. Synthesis of Substituted 6__H__‐Chromeno[4,3‐b]indolizines and their Aza‐analogues
We have synthesized a series of substituted chromeno[4,3‐b]indolizines and their respective aza‐analogues. Dyes generated from them contain the electrondonating 2‐(2‐hydroxy‐5‐methylphenyl)indolizin‐3‐yl moiety. The 90 MHz FT ^1^H‐NMR spectra of starting and final products supported the postulated structures. Fragmentations in the mass spectra also were consistent with the assumed structures.
📜 SIMILAR VOLUMES
Halochrome Molekeln. 6. Mitteilung. Spek
✍
Sigmund Gunzenhauser; Heinz Balli
📂
Article
📅
1985
🏛
John Wiley and Sons
🌐
German
⚖ 377 KB