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Karl Pfleger Walter Fuchs Prof. Dr. Matthias Pailer 《Monatshefte für Chemie / Chemical Monthly》1977,108(2):459-467
The synthesis of disubstituted pyridines by radical reactions and their respective reactivities are reported. 相似文献
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Karl Pfleger Walter Fuchs Matthias Pailer 《Monatshefte für Chemie / Chemical Monthly》1978,109(3):597-602
The synthesis of benzyl and phenethyl substituted 3-pyridine carbonitriles and 3-pyridine carboxylic acid methylesters resp. by homolytic alkylation is reported. 相似文献
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Regiospecific Synthesis of (Polyhydroxypropyl)-pterins: Synthesis of D -Anapterin and L -Primapterin Condensation of 2,5,6-triaminopyrimidin-4-one( 5 ) with the semicarbazone of pentoses proceeds regiospecifically with formation of 7-(polyhydroxypropyl)pterins. D -Anapterin (=7-(D -erythro-1′,2′,3′-trihydroxypropyl)pterin; D - 3 ) was obtained in 40% yield, and L -primapterin (=7-(L -erythro-1′,2′-dihydroxypropyl)pterin; L - 4 )in 10% yield. 相似文献
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Zusammenfassung Von 2-Mercapto-4-methoxy-6-morpholino-1,3,5-triazin ausgehend wurde eine Reihe disubstituierter 1,3,5-Triazine mit verschiedenen funktionellen Gruppen synthetisiert.
2-Mercapto-4-methoxy-6-morpholino-1,3,5-triazine has been used as starting material for the synthesis of several disubstituted 1,3,5-triazines with different functional groups.相似文献
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Esam Khalifa Hans-Jürg Furrer Jost H. Bieri Max Viscontini 《Helvetica chimica acta》1978,61(7):2739-2743
Regiospecific deuteriation of folic acid Introduction of a nitroso function at the N (10)-position of folic acid activates the C(9)-hydrogen atoms in such a way, that the exchange of H with D at this position, in NaOD-solution, is extremely facilitated. This fact is utilized in the synthesis of 9,9-dideuterio-folic acid (IV), 7,9,9-trideuterio-folic acid (VII) and 7-deuterio-folic acid (IX). These three products are necessary for the 1H-NMR.-spectroscopical determination of the conformation of 5,6,7,8-tetrahydrofolic acid and its derivatives. 相似文献
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Industrial drug research is undergoing radical changes. Advances in molecular biology and gene technology have resulted in the development of test systems with which a very large number of substances can be screened for their biological activity. In order to keep pace with this high-throughput screening procedure, preparative chemists need to reconsider conventional synthetic strategies. 相似文献