CAS: 5108-96-3; Ammonium Pyrrolidine-1-Carbodithioate

相似化合物

25769-03-3 701-13-3 40398-36-5

上下游产品

CAS号123-75-1 四氢吡咯 | CAS号75-15-0 二硫化碳 | CAS号496-08-2 Dithiobis(pyrro...

四氢吡咯,二硫化碳置于ammonium Hydroxide体系中,用 乙醚 作为反应溶剂,化学反应 1.0H,以85%的收率获得产物吡咯烷二硫代甲酸铵盐
参考文献:吡咯烷二硫代氨基甲酸酯的锡(iv)配合物:合成,表征和抗真菌活性.
标题:吡咯烷二硫代氨基甲酸酯的锡(iv)配合物:合成,表征和抗真菌活性.
摘要:吡咯烷二硫代氨基甲酸铵[nh4 {s2Cn(ch2)4}]与sncl2,[sn(c6H5)2Cl2],[sn(c6H5)3Cl],[sn(c4H9)2Cl2]和[sn(c6H11)3Cl以高收率得到的化合物[sn {s2Cn(ch2)4} 2Cl2](1),[sn {s2Cn(ch2)4} 2Ph2](2),[sn {s2Cn(ch2)4} Ph3](3),[sn {s2Cn(ch2)4} 2 N-Bu2](4)和[sn {s2Cn(ch2)4} Cy3](5).通过红外,多核NMR(1H,13C {1H}和119Sn {1H})和119Sn Mossbauer光谱对复合物进行表征.另外,通过x射线晶体学确定4的晶体结构.锡(iv)配合物以及配体的体外抗真菌活性是在人致病性真菌白色念珠菌上进行的,浓度为0.025.0.050;0.100; 0.200;0.400;0.800;1.600和3
DOI:10.1016/j.Ejmech.2005.07.008

专利信息

专利号:US-2024182421-A1
优先权日:2021-03-19
标题 :Synthesis of endochin-like quinolones
发明人：RISCOE MICHAEL K; NILSEN AARON; JIN HAIHONG; POU SOVITJ; WINTER ROLF W; DODEAN ROZALIA ANA; LIEBMAN KATHERINE M
权利人:UNIV OREGON HEALTH & SCIENCE; US GOV VETERANS AFFAIRS
摘要:Described herein are new synthetic routes for production of Endochin-Like Quinolone (ELQ) compounds. Synthetic routes to 3-substituted 4(1H)-quinolones are presented that are amenable to industrial scale preparation. One herein presented approach is relatively short, does not require palladium, and involves no chromatographic separation. A second herein presented approach is similarly relatively short, does not require palladium, involves no chromatographic separation, and also avoids high vacuum distillation. Additionally, both approaches require no protecting group chemistry because the insoluble 4(1H)-quinolone is not formed until the final reaction step.

专利号:CN-110204558-B
优先权日:2014-08-15
标 题:Synthesis of cephalosporin compounds

专利号:WO-2022197979-A1
优先权日:2021-03-19
标题:Synthesis of endochin-like quinolones

专利号:EP-4308109-A1
优先权日:2021-03-19
标 题:Synthesis of endochin-like quinolones

专利号:CN-117042768-A
优先权日:2021-03-19
标题:Synthesis of doxine-like quinolones

专利号:WO-2024101431-A1
优先权日:2022-11-10
标 题:Method for synthesizing peptide
发明人：YANO SHINYA
权利人:SEKISUI MEDICAL CO LTD
摘要:The purpose of the present invention is to provide a method for synthesizing a peptide or a long-chain peptide that uses amino acids including an amino acid containing a certain number of hydrophobic amino acids and an amino acid with a functional group on a side chain, the method not including the addition of additional solvents and not reducing the efficiency of Fmoc amino acid condensation reactions or Fmoc removal reactions.　Provided is a method for synthesizing a peptide, the peptide containing one or more amino acids with a functional group on a side chain, 50% or more of a hydrophobic amino acid, and 10% or less of an amino acid in which an α amino group is a secondary amino group; or a peptide with 21 or more residues and containing one or more amino acids with a functional group on a side chain. The method comprises introducing a carrier for peptide synthesis expressed by the general formula (1) below into the side chain of the amino acid with the functional group on a side chain.