A variety of the protected O-[(3-deoxy-a-D-manno-2-octulopyranosyl)onic acid]-(2+4)-3-deoxy-D-marano-2octulosonic acid [a-Kdo-(2+4)-Kdo] derivatives have been synthesized starting from methyl [2-(trimethylsilyl)ethyl4,5,7,8-tetra-Oacetyl-3-deoxy-a-D-manno-2-octulopyranosid]onate. Some of these were
✦ LIBER ✦
Monastrol analogs: A synthesis of pyrazolopyridine, benzopyranopyrazolopyridine, and oxygen-bridged azolopyrimidine derivatives and their biological screening
✍ Scribed by Jan Svetlik; Lucia Veizerová; Thomas U. Mayer; Mario Catarinella
- Book ID
- 104004466
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 193 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0960-894X
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✦ Synopsis
A synthesis of novel pyrazolopyridine, benzopyranopyrazolopyridine, and oxygen-bridged pyrazolo-, tetrazolo-, benzimidazo-, and thiazolopyrimidines via Hantzsch- and Biginelli-like condensations has been developed. The ability of these compounds to inhibit Eg5 activity has been examined. The results indicate that synthetic manipulations in the monastrol thiourea moiety are inefficient.
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Makoto Kiso; Minoru Fujita; Yuji Ogawa; Hideharu Ishida; Akira Hasegawa
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1990
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Elsevier Science
🌐
English
⚖ 997 KB