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STUDIES ON THE SYNTHESIS OF QUINOLINE COMPOUNDS II. : Syntheses of Tricyclic Derivatives of 3-Carboxy-1-ethyl-4-oxo-1,4-dihydroquinolines

机译：喹啉化合物的合成研究II。：3-羧基-1-乙基-4-氧代-1,4-二氢喹啉的三环衍生物的合成

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Hirao Ichiro; Yamaguchi Masahiko; Takefuji Nobuo; Fujikura Yuzo;
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年度 1984
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1. STUDIES ON PYRIDONECARBOXYLIC ACIDS - V - A PRACTICAL SYNTHESIS OF ETHYL 6,7-DIFLUORO-1-METHYL-4-OXO-4H-[1,3]THIAZETO[3,2-A]QUINOLINE-3-CARBOXYLATE , A KEY INTERMEDIATE FOR THE NEW TRICYCLIC QUINOLONE, PRULIFLOXACIN (NM441) AND VERSATILE NEW SYNTHESE [J] . Matsuoka M., Makita Y., Ohmachi S., Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry . 1997,第6期

机译：吡啶酮羧酸的研究-V-关键中间体乙基6,7-二氟-1-甲基-4-氧-4-4- [1,3]噻吩并[3,2-A]喹啉-3-羧酸的合成对于新的三环喹诺酮，普鲁沙星（NM441）和多功能新合成
2. Novel ring transformation of quinolines to indole derivatives in two steps via 1,4-dihydroquinoline derivatives [J] . Michiharu Sugiura, Natsuyo Yamaguchi, Koosuke Asai, Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry . 2003,第33期

机译：通过1，4-二氢喹啉衍生物分两步将喹啉新型环转化为吲哚衍生物
3. EFFICIENT SYNTHESIS OF NOVEL TRICYCLIC BENZOXAZINE DERIVATIVE VIA RING OPENING OF EPOXIDE ALONG THE MP AND DFT STUDIES OF STRUCTURAL, SPECTROSCOPIC (IR, RAMAN, UV-VIS), THERMODYNAMIC, ORBITALS AND NLO PROPERTIES OF DESIRED TRICYCLIC BENZOXAZINE DERIVATIVE [J] . Mansha Asim, Fawad Zahoor Ameer, Maqbool Zahid Faisal, Journal of the Chilean Chemical Society . 2020,第2期

机译：通过沿着结构，光谱（Raman，UV-Vis），热力学，轨道和NLO性能的MP和DFT研究，通过环氧化物的开环的新型三环苯并恶嗪衍生物的高效合成所需三环苯并嗪衍生物的熔点和DFT研究
4. Synthesis and fluorescence quenching studies on a quinoline derivative in the presence of TNT [C] . Na He, Fachun Zhong, Yuanjie Shu, Seminar on New Trends in Research of Energetic Materials;NTREM '12 . 2012

机译：TNT存在下喹啉衍生物的合成及荧光猝灭研究
5. I. A1,3- strain enabled retention of chirality during Bis-cyclization of β-ketoamides: Asymmetric synthesis and bioactivity of salinosporamide a and derivatives II. Optimization of an Organic syntheses procedure: asymmetric nucleophile-catalyzed aldol-lactonization with aldehyde acids [D] . Nguyen, Henry 2010

机译：I. A1,3-菌株能够在β-酮基酰胺的双环化过程中保留手性：salinosporamide a和衍生物II的不对称合成和生物活性。有机合成程序的优化：醛酸不对称亲核催化醛醇内酯化
6. Multicomponent reaction-based synthesis and biological evaluation of tricyclic heterofused quinolines with multi-trypanosomatid activity [O] . Ornella Di Pietro, Esther Vicente-García, Martin C. Taylor, -1

机译：基于多组分反应的具有多锥虫活性的三环杂稠喹啉的合成及生物学评价
7. STUDIES ON THE SYNTHESIS OF QUINOLINE COMPOUNDS III. : Syntheses of Tricyclic Aromatic Compounds with Two Parts of 3-Carboxy-1-ethyl-4-oxo-1,4-dihydropyridine [O] . Hirao Ichiro, Yamaguchi Masahiko, Takefuji Nobuo, 1984

机译：喹啉化合物的合成研究III。：具有两个部分的3-羧-1-乙基-4-氧代-1,4-二氢吡啶的三环芳族化合物的合成
8. Study on Synthesis of N-Nitroborazine Compounds. II. Borazine Derivatives. [R] . hirata, t. 1971

机译：N-硝基嗪类化合物的合成研究。 II。 Borazine衍生物。

STUDIES ON THE SYNTHESIS OF QUINOLINE COMPOUNDS II. : Syntheses of Tricyclic Derivatives of 3-Carboxy-1-ethyl-4-oxo-1,4-dihydroquinolines

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