| dc.contributor.author | Takahashi, Keisuke | |
| dc.contributor.author | Ikenaka, Yoshinori | |
| dc.contributor.author | Tsurumi, Tatsuya | |
| dc.contributor.author | Inami, Moe | |
| dc.contributor.author | Li, Zui | |
| dc.date.accessioned | 2019-07-22T11:02:57Z | |
| dc.date.available | 2019-07-22T11:02:57Z | |
| dc.date.issued | 2019 | |
| dc.identifier.citation | Takahashi, K. et al. 2019. Syntheses of 4‐OH and 5‐OH imidacloprids. ChemistrySelect, 4(24):7343-7345. [https://doi.org/10.1002/slct.201901491] | en_US |
| dc.identifier.issn | 2365-6549 (Online) | |
| dc.identifier.uri | http://hdl.handle.net/10394/32940 | |
| dc.identifier.uri | https://onlinelibrary.wiley.com/doi/10.1002/slct.201901491 | |
| dc.identifier.uri | https://doi.org/10.1002/slct.201901491 | |
| dc.description.abstract | 4‐OH and 5‐OH imidacloprids, important metabolites of neonicotinoid insecticides, were synthesised in 4 steps starting from S‐methylisothiourea sulfate. The structure of 4‐OH imidacloprid was determined by X‐ray crystallographic analysis. This is the first example of the synthesis of both metabolites independently | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Wiley | en_US |
| dc.subject | Imidacloprid | en_US |
| dc.subject | Insecticide | en_US |
| dc.subject | Metabolite | en_US |
| dc.subject | Neonicotinoid | en_US |
| dc.title | Syntheses of 4‐OH and 5‐OH imidacloprids | en_US |
| dc.type | Article | en_US |
| dc.contributor.researchID | 27878368 - Ikenaka, Yoshinori | |
