| LDR | | 01921nam u200409 4500 |
| 001 | | 000000418898 |
| 005 | | 20190215163237 |
| 008 | | 181129s2017 |||||||||||||||||c||eng d |
| 020 | |
▼a 9780438098381 |
| 035 | |
▼a (MiAaPQ)AAI10901899 |
| 035 | |
▼a (MiAaPQ)OhioLINK:osu1512079123614577 |
| 040 | |
▼a MiAaPQ
▼c MiAaPQ
▼d 247004 |
| 082 | 0 |
▼a 540 |
| 100 | 1 |
▼a Akwaboah, Daniel Clement. |
| 245 | 10 |
▼a Synthetic Study of Amphidinolides C, C2, C3, and F: Construction of the C1--C9 and the C10--C25 Building Blocks. |
| 260 | |
▼a [S.l.]:
▼b The Ohio State University.,
▼c 2017. |
| 260 | 1 |
▼a Ann Arbor:
▼b ProQuest Dissertations & Theses,
▼c 2017. |
| 300 | |
▼a 333 p. |
| 500 | |
▼a Source: Dissertation Abstracts International, Volume: 79-12(E), Section: B. |
| 500 | |
▼a Adviser: Craig Forsyth. |
| 502 | 1 |
▼a Thesis (Ph.D.)--The Ohio State University, 2017. |
| 520 | |
▼a Amphidinolides C, C2, C3, and F are cytotoxic secondary metabolites that occur naturally from symbiotic marine dinoflagellates Amphidinium sp. from the Okinawan flatworm. They share an identical 25-membered macrolide core that possesses 11 ster |
| 520 | |
▼a Our contribution to the amphidinolide project was designed to assemble a common macrolide framework which could be elaborated with minimal synthetic manipulations to access all four target molecules. We recognized a hidden structural homology th |
| 590 | |
▼a School code: 0168. |
| 650 | 4 |
▼a Chemistry. |
| 650 | 4 |
▼a Organic chemistry. |
| 690 | |
▼a 0485 |
| 690 | |
▼a 0490 |
| 710 | 20 |
▼a The Ohio State University.
▼b Chemistry. |
| 773 | 0 |
▼t Dissertation Abstracts International
▼g 79-12B(E). |
| 773 | |
▼t Dissertation Abstract International |
| 790 | |
▼a 0168 |
| 791 | |
▼a Ph.D. |
| 792 | |
▼a 2017 |
| 793 | |
▼a English |
| 856 | 40 |
▼u http://www.riss.kr/pdu/ddodLink.do?id=T15000312
▼n KERIS
▼z 이 자료의 원문은 한국교육학술정보원에서 제공합니다. |
| 980 | |
▼a 201812
▼f 2019 |
| 990 | |
▼a ***1012033 |