A general strategy for diverse syntheses of anhydrolandomycinone, tetrangulol, and landomycinone
| dc.citation.epage | 1888 | en_US |
| dc.citation.spage | 1885 | en_US |
| dc.citation.volume | 54 | en_US |
| dc.contributor.author | Sie, Cheng-Jhe | en_US |
| dc.contributor.author | Patteti, Venukumar | en_US |
| dc.contributor.author | Yang, Yi-Ru | en_US |
| dc.contributor.author | Mong, Kwok-Kong Tony | en_US |
| dc.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | en_US |
| dc.date.accessioned | 2018-08-21T05:53:19Z | |
| dc.date.available | 2018-08-21T05:53:19Z | |
| dc.date.issued | 2018-02-21 | en_US |
| dc.description.abstract | A general synthetic strategy based on a protecting group-promoted CH arylation method was developed for total syntheses of anhydro-landomycinone (1), tetrangulol (2), and landomycinone (3) from the same set of starting materials. | en_US |
| dc.identifier.doi | 10.1039/c7cc09818a | en_US |
| dc.identifier.issn | 1359-7345 | en_US |
| dc.identifier.journal | CHEMICAL COMMUNICATIONS | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1039/c7cc09818a | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/144530 | |
| dc.identifier.wosnumber | WOS:000425192800017 | en_US |
| dc.language.iso | en_US | en_US |
| dc.title | A general strategy for diverse syntheses of anhydrolandomycinone, tetrangulol, and landomycinone | en_US |
| dc.type | Article | en_US |
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