Synthesis of Key Fragments Contained in the Framework of Amphidinol 3

Bibliographic Details
Main Author: Bedore, Matthew William
Language:English
Published: The Ohio State University / OhioLINK 2008
Subjects:
Online Access:http://rave.ohiolink.edu/etdc/view?acc_num=osu1211485773
id ndltd-OhioLink-oai-etd.ohiolink.edu-osu1211485773
record_format oai_dc
spelling ndltd-OhioLink-oai-etd.ohiolink.edu-osu12114857732021-08-03T05:53:49Z Synthesis of Key Fragments Contained in the Framework of Amphidinol 3 Bedore, Matthew William Chemistry amphidinol 3 Julia-Kocienski olefination polyene marine polyketide <p>Amphidinol 3 was isolated from the marine dinoflagellate Amphidinium Klebsii found off the shores of Kanagawa, Japan. Structurally, amphidinol 3 (AM3) features a skipped northern polyene chain, a highly oxygenated central THP core, and a southern polyol chain containing a series of 1,5 diols. The 67-carbon backbone houses a total of 25 stereogenic centers and 8 (E) olefins.</p><p>Biologically, AM3 has the highest activity of the known 15 isolated members of the amphidinol family and possesses antifungal and hemolytic activities. Comparison to two other potent polyene antiobiotics, amphotocerin B (AmB) and filipin III, proved that AM3 exhibited both channel-type and damage-type hemolytic properties. Furthermore, the pore size created by AM3 in a cell membrane resembles that of cationic amine natural products of which AM3 shares virtually no similar defining structural characteristics. </p><p>The synthesis of the C1-C30 irregular polyol domain of AM3 was accomplished using the pathway originally developed by Chang with strategic optimization and alteration of the route. The readily available D and L-malic acids were utilized to construct large portions of the polyol chain and highly stereoselective methods were usedto elaborate these fragments. The coupling of the polyol components took place using the highly efficient Julia-Kocienski olefination to form the fully protected backbone.</p><p>The highly oxygenated C31-C52 central core of AM3 was synthesized from two THP fragments that were coupled via the Nozaki-Hiyama-Kishi reaction. The construction of the THP fragments was realized through a central intermediate in order to take advantage of the partial symmetry of the molecule. The readily available D-ribose served as a means for assembling the common intermediate.</p><p>After synthesis of the C53-C67 skipped polyene chain, the three major fragments of AM3 were completed. The union of these fragments via the highly selective Julia- Kocienski olefination to form the fully protected version of AM3 was explored with ultimate assembly of the C31-C67 fragment. Progress toward the complete total synthesis of this unique marine polyketide will also be reported.</p> 2008-08-21 English text The Ohio State University / OhioLINK http://rave.ohiolink.edu/etdc/view?acc_num=osu1211485773 http://rave.ohiolink.edu/etdc/view?acc_num=osu1211485773 unrestricted This thesis or dissertation is protected by copyright: all rights reserved. It may not be copied or redistributed beyond the terms of applicable copyright laws.
collection NDLTD
language English
sources NDLTD
topic Chemistry
amphidinol 3
Julia-Kocienski olefination
polyene
marine polyketide
spellingShingle Chemistry
amphidinol 3
Julia-Kocienski olefination
polyene
marine polyketide
Bedore, Matthew William
Synthesis of Key Fragments Contained in the Framework of Amphidinol 3
author Bedore, Matthew William
author_facet Bedore, Matthew William
author_sort Bedore, Matthew William
title Synthesis of Key Fragments Contained in the Framework of Amphidinol 3
title_short Synthesis of Key Fragments Contained in the Framework of Amphidinol 3
title_full Synthesis of Key Fragments Contained in the Framework of Amphidinol 3
title_fullStr Synthesis of Key Fragments Contained in the Framework of Amphidinol 3
title_full_unstemmed Synthesis of Key Fragments Contained in the Framework of Amphidinol 3
title_sort synthesis of key fragments contained in the framework of amphidinol 3
publisher The Ohio State University / OhioLINK
publishDate 2008
url http://rave.ohiolink.edu/etdc/view?acc_num=osu1211485773
work_keys_str_mv AT bedorematthewwilliam synthesisofkeyfragmentscontainedintheframeworkofamphidinol3
_version_ 1719427322397851648