✦ LIBER ✦

183. The chemistry of fungi. Part X. The synthesis of 4-hydroxy-3-acetylcoumarins

✍ Scribed by Badcock, G. G. ;Dean, F. M. ;Robertson, Alexander ;Whalley, W. B.

Book ID: 115531078
Publisher: The Royal Society of Chemistry
Year: 1950
Weight: 849 KB
Category: Article
ISSN: 0368-1769
DOI: 10.1039/jr9500000903

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The chemistry of fungi. Part LXXI. Synth

The chemistry of fungi. Part LXXI. Synthesis of 3,5-dihydroxy-4-methylbenzoic acid

✍ Briggs, David R.; Whalley, W. Basil 📂 Article 📅 1976 🏛 Royal Society of Chemistry ⚖ 331 KB

Chemistry of Modified Flavonoids. Part 2

Chemistry of Modified Flavonoids. Part 24. Synthesis of 4-Aryloxy-3-(2-hydroxy-4-hydroxy/alkoxyphenyl)pyrazoles.

✍ V. V. Arkhipov; M. M. Garazd; M. N. Smirnov; V. P. Khilya 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 16 KB

The chemistry of fungi. Part LXX. Synthe

The chemistry of fungi. Part LXX. Synthesis of some xanthones

✍ Ellis, Rodney C.; Whalley, W. Basil; Ball, Kenneth 📂 Article 📅 1976 🏛 Royal Society of Chemistry ⚖ 926 KB

ChemInform Abstract: Chemistry of 3-Heta

ChemInform Abstract: Chemistry of 3-Hetarylcoumarins. Part 3. Synthesis and Aminomethylation of 7′-Hydroxy-3,4′-bicoumarins (III).

✍ Frasinyuk, M. S.; Bondarenko, S. P.; Khilya, V. P. 📂 Article 📅 2012 🏛 John Wiley and Sons ⚖ 32 KB

Anthracyclines. Part 3. The total synthe

Anthracyclines. Part 3. The total synthesis of 4-demethoxydaunomycin

✍ Broadhurst, Michael J.; Hassall, Cedric H.; Thomas, Gareth J. 📂 Article 📅 1982 🏛 Royal Society of Chemistry ⚖ 841 KB

The synthesis of novel crown ethers, par

The synthesis of novel crown ethers, part X, 4-propyl-and 3-ethyl-4-methylchromenone-crown ethers

✍ Esra Tiftikçi; ÇAkil Erk 📂 Article 📅 2004 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 60 KB

## Abstract Starting from ethyl propionylacetate, and ethyl 2‐ethylacetoacetate we prepared 4‐propyl‐7,8‐, 4‐propyl‐6,7‐, 3‐ethyl‐4‐methyl‐7,8‐ and 3‐ethyl‐4‐methyl‐6,7‐dihydroxy‐2__H__‐chromenones which were allowed to react with the bis‐dihalides or ditosylates of glycols in DMF/Na~2~CO~3~ to aff