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A Convenient Method for Synthesis of Novel Cyclic Ethers (1R,2R,3R,5S,7S,9R,12R)-3-(t-Butyldimethylsilyl)oxy-7-methoxymethyl-oxy-2,10-dimethyl-12-oxatricyclo [7.2.1.0^(5,12)] dodecane
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作者 JieYAN MinZHU 《Chinese Chemical Letters》 SCIE CAS CSCD 2005年第4期453-456,共4页
Novel cyclic esters (1R, 2R, 3R, 5S, 7S, 9R, 12R)-3-(t-butyldimethylsilyl)oxy-7- methoxymethyloxy-2, 10-dimethyl-12-oxatricyclo [7.2.1.05,12] dodecane were prepared when their precursor 1 was treated with SOCl2/pyri... Novel cyclic esters (1R, 2R, 3R, 5S, 7S, 9R, 12R)-3-(t-butyldimethylsilyl)oxy-7- methoxymethyloxy-2, 10-dimethyl-12-oxatricyclo [7.2.1.05,12] dodecane were prepared when their precursor 1 was treated with SOCl2/pyridine. A plausible mechanism was hypothesized. 展开更多
关键词 R 2R 3R 5S 7S 9R 12R)-3-(t-butyldimethylsilyl)oxy-7-methoxymethyloxy-2 10-dimethy-12-oxatricyclo [7.2.1.05 12] dodecane synthesis mechanism.
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红霉素A9(O-叔丁基二甲基硅)肟的合成 被引量:3
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作者 孙京国 冯玉玲 《精细化工》 EI CAS CSCD 北大核心 2007年第2期162-165,共4页
以红霉素A与盐酸羟胺反应得到红霉素A肟(EMAO,Ⅰ),再以叔丁基二甲基氯硅烷(TBDMSCl)与Ⅰ进行硅醚化反应制备红霉素A9(O-叔丁基二甲基硅)肟(TBDS—EMAO,Ⅱ)。研究了硅醚化反应的溶剂化作用,有机碱催化作用,Z、E异构体的活... 以红霉素A与盐酸羟胺反应得到红霉素A肟(EMAO,Ⅰ),再以叔丁基二甲基氯硅烷(TBDMSCl)与Ⅰ进行硅醚化反应制备红霉素A9(O-叔丁基二甲基硅)肟(TBDS—EMAO,Ⅱ)。研究了硅醚化反应的溶剂化作用,有机碱催化作用,Z、E异构体的活性。实验结果表明,含孤电子对的极性非质子溶剂及相应的有机碱催化剂有助于在含有多个羟基的Ⅰ中进行肟羟基的选择性硅醚化反应。硅醚化反应以THF为溶剂,室温,反应物浓度c(Ⅰ)=0.27—0.53mol/L,硅醚化试剂用量n(TBDMSCl):n(Ⅰ)=1.4:1,有机碱用量n(Et3N):n(Ⅰ)=2.2:1时,收率可达97%。用HPLC分析了产品及相应的异构体,Z-Ⅱ反应活性较E-Ⅱ高。用IR、1HNMR、13CNMR、EIMS以及元素分析确证了相关物质的结构。 展开更多
关键词 红霉素A9(O-叔丁基二甲基硅)肟 硅醚化 叔丁基二甲基氯硅烷
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(S)-4-叔丁基二甲基硅氧基-L-脯氨酰胺的合成 被引量:1
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作者 何龙 《西华师范大学学报(自然科学版)》 2007年第1期91-93,共3页
以光学活性反式-4-羟基-L-脯氨酸为原料,用苯甲氧羰酰基保护氨基,叔丁基二甲基,硅基保护羟基,然后与1,2-二苯基-2-氨基乙醇反应得到(S)-4-叔丁基二甲基硅氧基-N-苯甲氧羰酰-L-脯氨酰胺3,催化氢解得到(S)-4-叔丁基二甲基硅氧基-L-脯氨酰胺4.
关键词 反式-4-羟基-L-脯氨酸 叔丁基二甲基硅基 脯氨酰胺
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MTBSTFA derivatization-LC-MS/MS approach for the quantitative analysis of endogenous nucleotides in human colorectal carcinoma cells
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作者 Huixia Zhang Yan Li +5 位作者 Zheng Li Christopher Wai-Kei Lam Peng Zhu Caiyun Wang Hua Zhou Wei Zhang 《Journal of Pharmaceutical Analysis》 SCIE CAS CSCD 2022年第1期77-86,共10页
Endogenous ribonucleotides(RNs)and deoxyribonucleotides(dRNs)are important metabolites related to the pathogenesis of many diseases.In light of their physiological and pathological significances,a novel and sensitive ... Endogenous ribonucleotides(RNs)and deoxyribonucleotides(dRNs)are important metabolites related to the pathogenesis of many diseases.In light of their physiological and pathological significances,a novel and sensitive pre-column derivatization method with N-(t-butyldimethylsilyl)-N-methyltrifluoroacetamide(MTBSTFA)was developed to determine RNs and dRNs in human cells using high-performance liquid chromatography tandem mass spectrometry(HPLC-MS/MS).A one-step extraction of cells with 85%methanol followed by a simple derivatization reaction within 5 min at room temperature contributed to shortened analysis time.The derivatives of 22 nucleoside mono-,di-and tri-phosphates were retained on the typical C;column and eluted by ammonium acetate and acetonitrile in 9 min.Under these optimal conditions,good linearity was achieved in the tested calibration ranges.The lower limit of quantitation(LLOQ)was determined to be 0.1-0.4μM for the tested RNs and 0.001-0.1μM for dRNs.In addition,the precision(CV)was<15%and the RSD of stability was lower than 10.4%.Furthermore,this method was applied to quantify the endogenous nucleotides in human colorectal carcinoma cell lines HCT 116 exposed to 10-hydroxycamptothecin.In conclusion,our method has proven to be simple,rapid,sensitive,and reliable.It may be used for specific expanded studies on intracellular pharmacology in vitro. 展开更多
关键词 RIBONUCLEOTIDES Deoxyribonucleotides DERIVATIZATION N-(t-butyldimethylsilyl)-N-methyltrifluoroacetamide High-performance liquid chromatography tandem mass spectrometry
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合成(3R,4R)-3-[(1'R)-叔丁基二甲基硅氧乙基]-4-乙酰氧基-2-氮杂环丁酮的新方法 被引量:2
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作者 曹佳 陈智栋 钱广 《合成化学》 CAS CSCD 2015年第9期865-866,869,共3页
(3R,4R)-3-[(1'R)-叔丁基二甲基硅氧乙基]-4'-乙酰氧基-1-对甲氧基苯基-2-氮杂环丁酮依次经铋酸钠/浓硫酸体系氧化和亚硫酸氢钠还原,合成了培南类药物的重要中间体——(3R,4R)-3-[(1'R)-叔丁基二甲基硅氧乙基]-4-乙酰氧基-2... (3R,4R)-3-[(1'R)-叔丁基二甲基硅氧乙基]-4'-乙酰氧基-1-对甲氧基苯基-2-氮杂环丁酮依次经铋酸钠/浓硫酸体系氧化和亚硫酸氢钠还原,合成了培南类药物的重要中间体——(3R,4R)-3-[(1'R)-叔丁基二甲基硅氧乙基]-4-乙酰氧基-2-氮杂环丁酮(1),收率62%,纯度98%,其结构经1H NMR,IR和EI-MS表征。 展开更多
关键词 氮杂环丁酮 铋酸钠 中间体 合成
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Na_3PO_4·12H_2O选择性催化脱去芳香性叔丁基二甲基硅醚
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作者 孔军 陈寅生 严琳 《化学研究》 CAS 2013年第4期403-407,共5页
报道了以磷酸盐为催化剂选择性脱去芳香性叔丁基二甲基硅醚的方法.以DMF为溶剂,室温下在0.5质量分数的Na3PO4.12H2O催化下,能顺利地脱去芳香性叔丁基二甲基硅醚得到相应的酚类化合物,而不影响其他的保护基和官能团.
关键词 选择性脱保护 叔丁基二甲基硅 Na3PO4 12H2O
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