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四烃基二锡氧烷在酯化反应中的催化作用 总被引:4,自引:0,他引:4
1,1,3,3-四烃基二锡氧烷Ⅰ是一类有机锡氧簇合物,它在固相和液相中[1,2]均为二聚梯形层状结构,在有机合成中表现出特殊的催化活性,与其它含Sn—O键非簇类化合物相比,催化活性和选择性均有大幅度提高.该类化合物是酯交换、酯化、官能团保护和脱保护等反应的优良催化剂[3].本文合成了一系列四烃基二锡氧烷,并以乙酸与丁醇的酯化反应为例,研究其对该反应的催化作用. 相似文献
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四烃基二锡氧烷的催化缩醛化性能研究 总被引:9,自引:0,他引:9
合成了一系列含不同烃基和官能团的二锡氧烷,并考察了其对巴豆醛与乙二醇缩合反应的催化作用.结果表明,四烃基二锡氧烷是高效的缩醛化反应催化剂,烃基对催化活性的影响主要归因于其空间位阻效应.二锡氧烷结构中内外锡原子上的烃基都对反应有影响,直链烃基催化剂的活性高于环烃基催化剂,碳数少的直链烃基催化剂的活性高于碳数多的.二锡氧烷上桥联基团的活性顺序为NCS>CH3O>Cl>CH3COO.这与其同乙二醇取代反应的难易程度相关联.提出了巴豆醛与乙二醇的缩合反应机理图式. 相似文献
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通过氧化二烃基锡与二氯二烃基锡的反应,合成了不对称四烃基二锡氧烷[ClR2SnOSnR'2Cl]2 (R=Bu,Pr; R'=Me,Ph,Cy,Oct).通过对化合物1和5的X-衍射晶体结构分折,表明该类化合物在晶体状态 时是含有中心对称Sn2O2四元环的梯状二聚体,内环锡与外环锡均为五配位的畸变三角双锥构型. 相似文献
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四丁基二锡氧烷催化合成碳酸二酯类化合物的新方法 总被引:12,自引:0,他引:12
以四丁基二锡氧烷为催化剂,通过尿素的醇解反应,合成了四种\r\n高沸点碳酸二酯化合物.研究结果表明,尿素的第一步醇解反应较易进\r\n行,产物收率大于60%;第二步从氨基甲酸酯醇解变为碳酸二酯的反应\r\n较难进行.尿素醇解反应与所用的醇有密切的关系,其中尿素与苯甲醇\r\n醇解为碳酸二酯的反应最易进行,正己醇次之,而正辛醇反应最难进行\r\n.提高反应温度到195℃,以官能团为NCS的四丁基二锡氧烷代替官能团\r\n为Cl的四丁基二锡氧烷为催化剂时,适当提高醇的配比,尿素与正辛醇\r\n醇解为碳酸二酯的产物收率有较大的提高.提出了尿素醇解反应的可能\r\n机理. 相似文献
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二(三)苄基锡不饱和烃基膦酸酯的合成 总被引:15,自引:3,他引:15
合成了10种二(三)苄基锡不饱和烃基膦酸酯[(PhCH2)nSn]n-1O2P(O)R(n=2,3;R=—C≡CPh,—C≡CC5H11-n,—C≡CCH2OCH3,—C≡CCH2OC2H5,—CH=CClPh),利用元素分析、核磁共振氢谱和TG-DTA对其组成和结构进行了表征.初步生物活性测试表明,有些化合物具有较强的杀螨和杀菌活性 相似文献
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[structure: see text] We have evaluated the effects of microwave irradiation on the solid-phase synthesis of beta-peptides. Sequences designed to adopt the 14-helix, especially those containing the structure-promoting residue trans-2-aminocyclohexanecarboxylic acid (ACHC), suffer from poor synthetic efficiency under standard SPPS conditions. A comparison of microwave and conventional heating shows that both provide excellent synthetic results for shorter sequences; however, we identify a clear benefit from microwave irradiation for longer beta-peptides. 相似文献
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A successful application of microwave irradiation, in which phthalocyanines were synthesized under solventless conditions from 1,2-phthalonitrile or phthalic anhydride and urea in the presence of metal templates is described. It was found that in comparison with conventional heating, the microwave process is a very useful alternative for cyclotetramerization processes because of reduction of the reaction time, better yield, and easy-to-perform procedure. 相似文献
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Suzanne Peyrottes Franck Gallier Jérôme Béjaud Christian Périgaud 《Tetrahedron letters》2006,47(44):7719-7721
Sugar and nucleoside phosphonates have been prepared using a microwave-assisted reaction. The comparison of thermal and microwave experimental conditions of the Michaelis-Arbuzov reaction is reported. 相似文献
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Garcia-Martin F Hinou H Matsushita T Hayakawa S Nishimura S 《Organic & biomolecular chemistry》2012,10(8):1612-1617
A standardized and smooth protocol for solid-phase glycopeptides synthesis under microwave irradiation was developed. Double activation system was proved to allow for highly efficient coupling of Tn-Ser/Thr and bulky core 2-Ser/Thr derivatives. Versatility and robustness of the present strategy was demonstrated by constructing a Mucine-1 (MUC1) fragment and glycosylated fragments of tau protein. The success of this approach relies on the combination of microwave energy, a resin consisting totally of polyethylene glycol, a low excess of sugar amino acid and the "double activation" method. 相似文献
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A small library of benzoxazine-fused isoquinolines has been synthesized under microwave irradiation (MW) via CuI-catalyzed domino reactions of o-alkynyl aldehydes and amines having embedded nucleophiles. This strategy offers a operationally simple, environmentally acceptable route to synthesize benzoxazine-fused isoquinolines in moderate to good yields. All new compounds were characterized by 1H NMR, 13C NMR, infrared, and high-resolution mass spectrometry techniques. 相似文献
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A facile procedure for the synthesis.of quinoxalines is being reported starting from benzil and 1,2-diaminobenzene. Thereactions were carried out catalyst-free, solvent-free and under microwave irradiation conditions in high yield (84-98%) with short time (3-6 rain) and environmental benign, as well as convenient operation. The structures of all the compounds have been confirmed on the basis of their IR, 1H NMR, and/or 13C NMR, mass spectral data. 相似文献