Synthetic studies toward the total synthesis of azaspiracid-1 Public Deposited

http://ir.library.oregonstate.edu/concern/graduate_thesis_or_dissertations/7h149t10p

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  • Azaspiracid-1, a novel marine toxin that contains 9 rings and 20 stereogenic centers, has drawn considerable attention from synthetic groups worldwide due to its structural complexity, which includes a unique trioxabisspiroketal fused to a tetrahydrofuran ring (ABCD rings), a piperidine-tetrahydrofuran spiroaminal system fused to a 2,9-dioxabicyclo[3.3.1]nonane system (FGHI rings), a connecting six-membered cyclic hemiketal bridge (E ring) and a γ,δ-unsaturated terminal carboxylic acid side chain. Our efforts toward the total synthesis of azaspiracid-1 led to the completion of both C1-C26 northern and C27-C40 southern halves of azaspiracid-1. Herein, our improved and scalable synthetic studies toward the total synthesis of azaspiracid-1 is described. In particular, an improved and scalable synthesis of sulfone 3.6 with a key one-pot ketalization and methylation of ketone 3.22 to methylated hemiketal 3.24 is illustrated. A total 19 mmol of sulfone 3.6 has been prepared by this approach. An improved and scalable synthesis of aldehyde 3.7 utilizing allyl bromide 3.31 to couple with Evans auxiliary 3.33 has been developed. A total of 10 mmol of aldehyde 3.7 has been prepared by this approach. An improved synthesis toward the ABC ring fragment 3.52 with a high yield Julia coupling step is shown. Large scale improved syntheses of the linkage fragment 3.2, the aldehyde fragment 4.9 and the azide fragment 4.10 of the southern portion of (–)-azaspiracid-1 have been described. With an abundant material prepared by this scalable improved approach, we are confident that completing the total synthesis of (–)-azaspiracid-1 will occur in the near future.
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  • description.provenance : Approved for entry into archive by Julie Kurtz(julie.kurtz@oregonstate.edu) on 2012-07-06T16:22:47Z (GMT) No. of bitstreams: 2 SuDong2012.pdf: 1920374 bytes, checksum: b54c5eab7c55253bcc993fb64b03dd39 (MD5) supplemental NMR.pdf.pdf: 3302870 bytes, checksum: 71ddafcf6b4647e582ccd6cf76eac326 (MD5)
  • description.provenance : Rejected by Julie Kurtz(julie.kurtz@oregonstate.edu), reason: Rejecting to remove page numbers on the pretext pages. Also the title page needs to appear after the copyright page and before the approval page. Once revised, open the item that was rejected. Replace the attached file with the revised file and resubmit. Thanks, Julie on 2012-06-25T16:48:47Z (GMT)
  • description.provenance : Submitted by Dong Su (sud@onid.orst.edu) on 2012-06-24T05:21:57Z No. of bitstreams: 2 supplemental NMR.pdf.pdf: 3302870 bytes, checksum: 71ddafcf6b4647e582ccd6cf76eac326 (MD5) SuDong2012.pdf.pdf: 4329956 bytes, checksum: 889abd266174241ffd5c696a380eca54 (MD5)
  • description.provenance : Approved for entry into archive by Laura Wilson(laura.wilson@oregonstate.edu) on 2012-07-11T16:11:07Z (GMT) No. of bitstreams: 2 SuDong2012.pdf: 1920374 bytes, checksum: b54c5eab7c55253bcc993fb64b03dd39 (MD5) supplemental NMR.pdf.pdf: 3302870 bytes, checksum: 71ddafcf6b4647e582ccd6cf76eac326 (MD5)
  • description.provenance : Submitted by Dong Su (sud@onid.orst.edu) on 2012-06-28T04:39:03Z No. of bitstreams: 2 SuDong2012.pdf: 1920374 bytes, checksum: b54c5eab7c55253bcc993fb64b03dd39 (MD5) supplemental NMR.pdf.pdf: 3302870 bytes, checksum: 71ddafcf6b4647e582ccd6cf76eac326 (MD5)
  • description.provenance : Made available in DSpace on 2012-07-11T16:11:07Z (GMT). No. of bitstreams: 2 SuDong2012.pdf: 1920374 bytes, checksum: b54c5eab7c55253bcc993fb64b03dd39 (MD5) supplemental NMR.pdf.pdf: 3302870 bytes, checksum: 71ddafcf6b4647e582ccd6cf76eac326 (MD5) Previous issue date: 2012-05-31

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