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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

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✦ 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.


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Halochrome Molekeln. 6. Mitteilung. Spek
✍ Sigmund Gunzenhauser; Heinz Balli 📂 Article 📅 1985 🏛 John Wiley and Sons 🌐 German ⚖ 377 KB

**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