| dc.contributor.author | Kelley, Elizabeth H. (Elizabeth Helen) | |
| dc.contributor.author | Jamison, Timothy F | |
| dc.date.accessioned | 2021-11-24T16:24:33Z | |
| dc.date.available | 2021-09-20T18:22:10Z | |
| dc.date.available | 2021-11-24T16:24:33Z | |
| dc.date.issued | 2019 | |
| dc.identifier.uri | https://hdl.handle.net/1721.1/132391.2 | |
| dc.description.abstract | © 2019 American Chemical Society. Synthesis of the fused polycyclic ether motif comprising the EFG rings of the marine ladder polyethers tamulamides A and B has been achieved via two different etherification strategies. Ultimately, a reductive etherification approach proved most successful due to tolerance of the G ring substitution and provided the EFG 6,7,6 ring system in 58% yield. | en_US |
| dc.description.sponsorship | NIGMS (Grant GM72566) | en_US |
| dc.language.iso | en | |
| dc.publisher | American Chemical Society (ACS) | en_US |
| dc.relation.isversionof | 10.1021/ACS.ORGLETT.9B03015 | en_US |
| dc.rights | Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use. | en_US |
| dc.source | PMC | en_US |
| dc.title | Synthesis of the EFG Framework of Tamulamides A and B | en_US |
| dc.type | Article | en_US |
| dc.contributor.department | Massachusetts Institute of Technology. Department of Chemistry | en_US |
| dc.relation.journal | Organic Letters | en_US |
| dc.eprint.version | Author's final manuscript | en_US |
| dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
| eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
| dc.date.updated | 2020-10-19T14:45:52Z | |
| dspace.orderedauthors | Kelley, EH; Jamison, TF | en_US |
| dspace.date.submission | 2020-10-19T14:45:55Z | |
| mit.journal.volume | 21 | en_US |
| mit.journal.issue | 19 | en_US |
| mit.license | PUBLISHER_POLICY | |
| mit.metadata.status | Publication Information Needed | en_US |
