1991 Fiscal Year Final Research Report Summary
Enantioselective Syntheses of Natural Products based on a Biosynthetic Pathway
Project/Area Number |
01571139
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Research Category |
Grant-in-Aid for General Scientific Research (C)
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Allocation Type | Single-year Grants |
Research Field |
Chemical pharmacy
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Research Institution | Department of Pharmaceutical Science, Akita University |
Principal Investigator |
SUZUKI Toshio Akita University of Medicine, Pharmaceutical Science, Associate Professor, 医学部, 助教授 (20108559)
|
Co-Investigator(Kenkyū-buntansha) |
UNO Katsuo Akita University of Medicine, Pharmaceutical Science, Professor, 医学部, 教授
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Project Period (FY) |
1989 – 1991
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Keywords | D-Mannitol / L-Ascorbic acid / Claisen rearrangement / Cyclopentanone derivative / Steroid / (-)-Chokol A / Vitamin D_3 / Brefeldin A |
Research Abstract |
Enantioselective syntheses of various types of natural products were examined based on a biosynthetic pathway. Namely, four chiral cyclopentanone derivatives (1), (2), (3) and (4) were synthesized via 1, 2-0-isopropylideneglyceraldehyde from D-mannitol and L-ascorbic acid using Claisen rearrangement as a key step. <<chemical formula>> Trans-hydrindanone propion acid (5) bicyclo[3.3.0]octane (6) and (-)-chokol A (7) were synthesized from the compound (2). whereas de-AB-cholestane derivative (8). key intermediate for construction of vitamin D3. was obtained from the compound (4). During the course of the syntheses of steroids. fortunately. we are able to develop steroids possessing extremely strong anti-inflamatory activity and non pituitary adrenal suppression. so called -antedrug- and "pro-antedrug-". Furthermore. trans-hydrindanone (9) and cyclopentanone derivative (10) were synthesized by intramolecular ring opening of the corresponding epoxides. respectively. These cyclized products could also be important intermediates for construction of 1, 25(OH)_2 vitamin D_3 and brefeldin A possessing antifungal, antiviral and other biological activities.
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Research Products
(13 results)