Long-chain substituted chromones from two dianellinae
β Scribed by R.G. Cooke; J.G. Down
- Book ID
- 104248760
- Publisher
- Elsevier Science
- Year
- 1970
- Tongue
- French
- Weight
- 131 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
of petroleum extracts of roots of both Dianella revoluta and Stypandra -a series of compounds of general structure ( I 1, where R = C H 27 55 (n), C29H59(n), or C3,Hb3(nf. The compounds were characterised as a mixture of homologuea, and structures have been assigned on the basis of the evidence below. I 11 III Compounds ( I ) give an intense purple colour with ethanolic FeC13, as is typical for 5-hydroxychromones'. The homologues show absorption maxima at 232, 2$(sh), 260 and 301 tan, ( 1ogE 4.4, 4.25, 4.3 and 4.1 1, and minima at 244 and 276 mv ( log& 4.2 and 3.9 ). These values compare very closely with those for dihydropeuceniu ( II 1, but differ significantly from values for analogous 8-alkylchromones2.
π SIMILAR VOLUMES
An Efficient Synthesis of New Long-Chain Substituted Tetrathiafulvalene Derivatives Involving Two Tetrathiafulvalene Moieties -[preparation of (IV) and analogues such as (V)]. -(SUDMALE, I.;
## Abstract Review: 30 refs.