| pubmed-article:17452108 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:17452108 | lifeskim:mentions | umls-concept:C0003308 | lld:lifeskim |
| pubmed-article:17452108 | lifeskim:mentions | umls-concept:C0441655 | lld:lifeskim |
| pubmed-article:17452108 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
| pubmed-article:17452108 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
| pubmed-article:17452108 | lifeskim:mentions | umls-concept:C1958780 | lld:lifeskim |
| pubmed-article:17452108 | lifeskim:mentions | umls-concept:C1958781 | lld:lifeskim |
| pubmed-article:17452108 | lifeskim:mentions | umls-concept:C0243072 | lld:lifeskim |
| pubmed-article:17452108 | pubmed:issue | 12 | lld:pubmed |
| pubmed-article:17452108 | pubmed:dateCreated | 2007-5-8 | lld:pubmed |
| pubmed-article:17452108 | pubmed:abstractText | Starting from the key intermediate 5-(3,4,5-trimethoxyphenyl)-1,3,4-thiadiazole-2-thiol (4) or the oxadiazole analogue (5), the title compounds 9 and 10 are synthesized by a two-step process. Thioetherification reaction of 4 or 5 with an organic halide catalyzed by indium or indium tribromide first affords appropriate sulfide 7 or 8, which is then converted into title compounds 9 or 10 by hydrogen peroxide oxidation catalyzed by ammonium molybdate in ionic liquid [bmim]PF6. The structures are unequivocally confirmed by spectroscopic (IR, 1H and 13C NMR) data and elemental analyses. The structures of 8d and 10q are further established by X-ray crystallographic diffraction analysis. The compounds have been shown to be fungicidally active. Title compounds 10i and 10j can inhibit mycelia growth by approximately 50% (EC50) at 2.9-93.3 microg/mL in vitro against 10 kinds of fungi. | lld:pubmed |
| pubmed-article:17452108 | pubmed:language | eng | lld:pubmed |
| pubmed-article:17452108 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17452108 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:17452108 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17452108 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17452108 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17452108 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:17452108 | pubmed:month | Jun | lld:pubmed |
| pubmed-article:17452108 | pubmed:issn | 0968-0896 | lld:pubmed |
| pubmed-article:17452108 | pubmed:author | pubmed-author:DadoDD | lld:pubmed |
| pubmed-article:17452108 | pubmed:author | pubmed-author:MokM MMM | lld:pubmed |
| pubmed-article:17452108 | pubmed:author | pubmed-author:ChenZhuoZ | lld:pubmed |
| pubmed-article:17452108 | pubmed:author | pubmed-author:SongYangY | lld:pubmed |
| pubmed-article:17452108 | pubmed:author | pubmed-author:LuPingP | lld:pubmed |
| pubmed-article:17452108 | pubmed:author | pubmed-author:HuDe-YuDY | lld:pubmed |
| pubmed-article:17452108 | pubmed:author | pubmed-author:SongBao-AnBA | lld:pubmed |
| pubmed-article:17452108 | pubmed:author | pubmed-author:JinLin-HongLH | lld:pubmed |
| pubmed-article:17452108 | pubmed:author | pubmed-author:XuGuang-FangG... | lld:pubmed |
| pubmed-article:17452108 | pubmed:author | pubmed-author:BhaduryPinaki... | lld:pubmed |
| pubmed-article:17452108 | pubmed:author | pubmed-author:ChenCai-JunCJ | lld:pubmed |
| pubmed-article:17452108 | pubmed:author | pubmed-author:LiQian-ZhuQZ | lld:pubmed |
| pubmed-article:17452108 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:17452108 | pubmed:day | 15 | lld:pubmed |
| pubmed-article:17452108 | pubmed:volume | 15 | lld:pubmed |
| pubmed-article:17452108 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:17452108 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:17452108 | pubmed:pagination | 3981-9 | lld:pubmed |
| pubmed-article:17452108 | pubmed:meshHeading | pubmed-meshheading:17452108... | lld:pubmed |
| pubmed-article:17452108 | pubmed:meshHeading | pubmed-meshheading:17452108... | lld:pubmed |
| pubmed-article:17452108 | pubmed:meshHeading | pubmed-meshheading:17452108... | lld:pubmed |
| pubmed-article:17452108 | pubmed:meshHeading | pubmed-meshheading:17452108... | lld:pubmed |
| pubmed-article:17452108 | pubmed:meshHeading | pubmed-meshheading:17452108... | lld:pubmed |
| pubmed-article:17452108 | pubmed:meshHeading | pubmed-meshheading:17452108... | lld:pubmed |
| pubmed-article:17452108 | pubmed:meshHeading | pubmed-meshheading:17452108... | lld:pubmed |
| pubmed-article:17452108 | pubmed:meshHeading | pubmed-meshheading:17452108... | lld:pubmed |
| pubmed-article:17452108 | pubmed:meshHeading | pubmed-meshheading:17452108... | lld:pubmed |
| pubmed-article:17452108 | pubmed:year | 2007 | lld:pubmed |
| pubmed-article:17452108 | pubmed:articleTitle | Synthesis and antifungal activities of 5-(3,4,5-trimethoxyphenyl)-2-sulfonyl-1,3,4-thiadiazole and 5-(3,4,5-trimethoxyphenyl)-2-sulfonyl-1,3,4-oxadiazole derivatives. | lld:pubmed |
| pubmed-article:17452108 | pubmed:affiliation | Center for Research and Development of Fine Chemicals, Key Laboratory of Green Pesticide and Bioengineering, Ministry of Education, Guizhou University, Guiyang 550025, PR China. | lld:pubmed |
| pubmed-article:17452108 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:17452108 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| http://linkedlifedata.com/r... | http://linkedlifedata.com/r... | pubmed-article:17452108 | lld:chembl |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:17452108 | lld:pubmed |
