## Isocoumarins I Ring-chain tautomerism I Peniophora sanguinea The structure (?)-3,6,8-trihydroxy-3-pentadecyl-3,4-dihy-by total synthesis of this compound and some of its derivatidroisocoumarin 1 assigned by earlier workers to peniolactol, a metabolite of Peniophora sunguinea, has been confirmed
The Synthesis of Some 1, 8-Phenanthrolines and Related Compounds
✍ Scribed by Diether G. Markees
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- German
- Weight
- 353 KB
- Volume
- 66
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
The synthesis of ethyl 4‐oxo‐1, 4‐dihydro‐1, 8‐phenanthroline‐3‐carboxylate (2a) and some other 1, 8‐phenanthrolines is reported. The ethylation of the above ester yields a thermochromic product 2b and some ethyl 4‐ethoxy‐1, 8‐phenanthroline‐3‐carboxylate (3b). Reexamination of similar ethylations of analogous esters derived from 1, 7‐phenanthroline and 1, 10‐phenanthroline indicated formation of the O‐ethyl derivative of the former and the N‐ethyl derivative of the latter.
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## Abstract 1,1′‐Thiobis (2‐hydroxyethane) has been synthesized isotopically labelled with sulphur‐35, carbon‐13 and deuterium. The conversion to 1,1′‐thiobis (2‐chloroethane) labelled with sulphur‐35 and carbon‐13 is described.