Project/Area Number |
03670999
|
Research Category |
Grant-in-Aid for General Scientific Research (C)
|
Allocation Type | Single-year Grants |
Research Field |
Chemical pharmacy
|
Research Institution | Osaka University |
Principal Investigator |
KITA Yasuyuki Osaka University, Faculty of Pharmaceutical Sciences, Professor, 薬学部, 教授 (00028862)
|
Project Period (FY) |
1991 – 1992
|
Project Status |
Completed (Fiscal Year 1992)
|
Budget Amount *help |
¥2,100,000 (Direct Cost: ¥2,100,000)
Fiscal Year 1992: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 1991: ¥1,300,000 (Direct Cost: ¥1,300,000)
|
Keywords | discorhabdin / antitumor activity / marine natural Product / total synthesis / hypervalent iodine reagent / aminoindoloquinone imine system / azacarbocyclic spiro dienone system / discorhabdin |
Research Abstract |
The discorhabdin alkaloids (discorhabdin A-D) were isolated from the sponge of Latrunculia du Bocage in New Zealand and exhibit extreme toxicity toward tumor cells (P388 and L2110 leukemia). These novel molecules have a unique molecular skeleton incorporating an azacarbocyclic dibromospirohexadienone system and a highly oxidized indol system in which the tryptamine side chain is cyclized onto an indoloquinone. Recently, much attention has been paid to the total synthesis of these challenging targets. As a part of our continuous studies on hypervalent iodine chemistry, we have established a general route to the azacarbocyclic spiro dienone systems by an oxidative coupling reaction of the O-silylated phenol derivatives bearing both electron-poor and electron-rich aminoquinones at the para position, using phenyliodine(III) bis(trifluoroacetate)(PIFA). This method was applied to the first total synthesis of discorhabdin C. During this synthesis, a new effective method for the aminoindoloquinone imine systems was also developed. The synthetic studies of the other discorhabdin alkaloids (A,B,D), which have the thioether bonds in the molecule are still on line, including development of a new synthetic method for the optically active thioether bond formation.
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