The "Electrophilic" trichloromethyl radical was introduced directly into the model purine compound, caffeine, leading to products 2 and 3 (the former being smoothly converted to the corresponding carboxy ester derivative) ana to the unexpected C-5 substituted title compound 4. -Extensive investigati
Controlled C-5 methylation of caffeine by benzoyloxy radical addition at C-8
β Scribed by J Zylber; L Ouazzani-Chahdi; A Chiaroni; C Riche
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- French
- Weight
- 213 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0040-4039
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Addition of carbon radicals generated from organoselenium reagents P SeR: R= COPh, CO\*Et, CH,CO,Et, CH2COMe, and CH,CN) to 4',5'-unsaturated uraciinucleosides was found to provide a highly efficient entry to C-C bond formation at the 5'-position, the stereochemical outcome of which is dependent upo
## Abstract For Abstract see ChemInform Abstract in Full Text.
Highly Functionalized Cyclopentanes by Radical Cyclization of Unsaturated Bromolactones. Part 3. Preparation of Carbaaldohexofuranoses. Determination of the Relative Configuration at C-4/C-5 or 2,3-Unsaturated Heptono-1,4-lactones by Means of 1 H NMR Spectroscopy. -Key step in the synthesis of carb