Title of article :
Total synthesis and adjuvant activity of all stereoisomers of pinellic acid
Author/Authors :
Tatsuya Shirahata، نويسنده , , Toshiaki Sunazuka، نويسنده , , Kiminari Yoshida، نويسنده , , Daisuke Yamamoto، نويسنده , , Yoshihiko Harigaya، نويسنده , , Takayuki Nagai، نويسنده , , Hiroaki Kiyohara، نويسنده , , Haruki Yamada، نويسنده , , Isao Kuwajima، نويسنده , , Satoshi mura، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2003
Pages :
5
From page :
937
To page :
941
Abstract :
Pinellic acid is a novel and potentially useful oral adjuvant when used in conjunction with intranasal inoculation of influenza HA vaccines. All stereoisomers of pinellic acid have been synthesized via regioselective asymmetric dihydroxylation, regioselective inversion, and stereoselective reduction, and their adjuvant activities were characterized. Among this series of isomers, 9S, 12S, 13S compound has the most potent adjuvant activity. Structure–activity relationships are discussed.
Journal title :
Bioorganic & Medicinal Chemistry Letters
Serial Year :
2003
Journal title :
Bioorganic & Medicinal Chemistry Letters
Record number :
793049
Link To Document :
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