首页--数理科学和化学论文--化学论文--有机化学论文

含氮杂环的芳构化反应研究及其在β-咔啉生物碱合成中的应用

Abstract第6页
摘要第8-14页
Chapter 1.Introduction第14-18页
    1.1 β-Carbolines第14页
    1.2 Imidazoles第14-15页
    1.3 Pyrimidines第15页
    1.4 Eudistomins Y_1-Y_7第15-16页
    1.5 Cordysinins C & D第16页
    1.6 Eudistomin U第16-17页
    1.7 Eudistomin I第17页
    1.8 Alangiobussinine第17-18页
Chapter 2.Aromatization of 1,2,3,4-tetra(or 3,4-di)hydro-β-carbolines第18-36页
    2.1 Review of synthetic methods for β-carbolines第18-27页
    2.2 Results and Discussion第27-33页
        2.2.1 Aromatization of 3,4-dihydro-β-carbolines第27-30页
        2.2.2 Aromatization of 1,2,3,4-tetrahydro-β-carbolines第30-33页
    2.3 Mechanism第33-35页
    2.4 Conclusion第35-36页
Chapter 3. Aromatization of imidazolines第36-50页
    3.1 Review of synthetic methods for imidazoles第36-44页
    3.2 Results and Discussion第44-48页
    3.3 Mechanism第48-49页
    3.4 Conclusion第49-50页
Chapter 4.Aromatization of 1,4,5,6-tetrahydro-pyrimidines第50-66页
    4.1 Review of synthetic methods for pyrimidines第50-61页
    4.2 Results and Discussion第61-64页
    4.3 Mechanism第64-65页
    4.4 Conclusion第65-66页
Chapter 5.Application for total syntheses of several β-carboline alkaloids第66-81页
    5.1 Syntheses of eudistomins Y_1-Y_7第66-71页
        5.1.1 Review of synthetic methods for eudistomins Y_1-Y_7第66-68页
        5.1.2 Results and Discussion第68-71页
        5.1.3 Conclusion第71页
    5.2 Syntheses of cordysinins C & D第71-73页
        5.2.1 Review of synthetic methods for cordysinins C & D第71页
        5.2.2 Results and Discussion第71-73页
        5.2.3 Conclusion第73页
    5.3 Synthesis of eudistomin U第73-77页
        5.3.1 Review of synthetic methods for eudistomin U第73-75页
        5.3.2 Results and Discussion第75-77页
        5.3.3 Conclusion第77页
    5.4 Synthesis of eudistomin I第77-79页
        5.4.1 Review of synthetic methods for eudistomin I第77-78页
        5.4.2 Results and Discussion第78-79页
        5.4.3 Conclusion第79页
    5.5 Synthesis of alangiobussinine第79-81页
        5.5.1 Review of synthetic methods for alangiobussinine第79-80页
        5.5.2 Results and Discussion第80页
        5.5.3 Conclusion第80-81页
Chapter 6. Summary第81-88页
    6.1 Aromatization of 3,4-dihydro-β-carbolines第81-82页
    6.2 Aromatization of 1,2,3,4-tetrahydro-β-carbolines第82页
    6.3 Aromatization of imidazolines第82-83页
    6.4 Aromatization of 1,4,5,6-tetrahydro-pyrimidines第83页
    6.5 Total syntheses of eudistomins Y_1-Y_7第83-84页
    6.6 Total syntheses of cordysinins C & D第84-85页
    6.7 Total synthesis of eudistomin U第85-86页
    6.8 Total synthesis of eudistomin I第86-87页
    6.9 Total synthesis of alangiobussinine第87-88页
Chapter 7. Experimental Section第88-152页
    General Method第88页
    7.1 Aromatization of 3,4-dihydro-β-carbolines第88-97页
        7.1.1 Aromatization of 3,4-dihydro-β-carbolines with electron-withdrawing groups第88-91页
        7.1.2 Aromatization of 3,4-dihydro-β-carbolines without electron-withdrawing groups第91-97页
    7.2 Aromatization of 1,2,3,4-tetrahydro-β-carbolines第97-102页
    7.3 Aromatization of imidazolines第102-111页
        7.3.1 Method 3.1第102-110页
        7.3.2 Method 3.2第110-111页
    7.4 Aromatization of 1,4,5,6-tetrahydro-pyrimidines第111-122页
        7.4.1 The preparation of N-tosyl-1,4,5,6-tetrahydro-pyrimidines第111-113页
        7.4.2 The preparation of pyrimidines第113-122页
    7.5 Total syntheses of several β-carboline alkaloids第122-152页
        7.5.1 Total syntheses of cudistomins Y_1-Y_7第122-135页
        7.5.2 Total syntheses of cordysinins C & D第135-143页
        7.5.3 Total synthesis of eudistomin U第143-147页
        7.5.4 Total synthesis of eudistomin I第147-149页
        7.5.5 Synthesis of alangiobussinine第149-152页
References第152-160页
Acknowledgments第160-161页
Appendix 1. List of new compounds第161-168页
Appendix 2. Published articles第168页

论文共168页,点击 下载论文
上一篇:异吲哚啉衍生物的合成及其抑制NR2B Ca2+流量研究和通关藤和牛角瓜的化学成分研究
下一篇:废水中邻苯二胺强化去除技术研究