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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 📂 Article 📅 1990 🏛 Elsevier Science 🌐 English ⚖ 997 KB

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