Highly enantioselective 1,3 dipolar cyloaddition of azomethine imines and an application to a formal total synthesis of manzacidin c
➤ Gửi thông báo lỗi ⚠️ Báo cáo tài liệu vi phạmNội dung chi tiết: Highly enantioselective 1,3 dipolar cyloaddition of azomethine imines and an application to a formal total synthesis of manzacidin c
Highly enantioselective 1,3 dipolar cyloaddition of azomethine imines and an application to a formal total synthesis of manzacidin c
DissertationHighly Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Imines and an Application to a Formal Total Synthesis of Manzacidin cGradu Highly enantioselective 1,3 dipolar cyloaddition of azomethine imines and an application to a formal total synthesis of manzacidin c uate School ofNatural Science & TechnologyKanazawa UniversityDivision of Material ChemistryStudent ID Number : 1424022003Name : Tong Thi Minh ThuChief advisor: Prof. Dr. Yutaka UkajiFebruary. 2017ACKNOWLEDGEMENTSFirst of all. I would like to express my sincere thanks to the Vietnamese Government has Highly enantioselective 1,3 dipolar cyloaddition of azomethine imines and an application to a formal total synthesis of manzacidin c given me a great chance to pursue an international doctoral course by their financial support, under a Vietnam International Education Development CaHighly enantioselective 1,3 dipolar cyloaddition of azomethine imines and an application to a formal total synthesis of manzacidin c
mpaign.I wish to show my deep gratitude to Ba Ria-Vung Tau University, the place I have been working, has recommended me to apply the Vietnamese scholDissertationHighly Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Imines and an Application to a Formal Total Synthesis of Manzacidin cGradu Highly enantioselective 1,3 dipolar cyloaddition of azomethine imines and an application to a formal total synthesis of manzacidin c he staff members of: Graduate School of Natural Science & Technology. Division of Student Affaks. Division of Material Chemistry for essential guidance and enthusiastic support throughout the period of my life and study in Japan.I would like to express my profound gratitude to my advisor - Prof. Dr. Highly enantioselective 1,3 dipolar cyloaddition of azomethine imines and an application to a formal total synthesis of manzacidin c Yutaka Ukaji. Words do not seem sufficient to let him know 1 have deep feelings for everything he graciously taught for me during my study. I treasurHighly enantioselective 1,3 dipolar cyloaddition of azomethine imines and an application to a formal total synthesis of manzacidin c
e the beautiful things he did for international students that touched me. With my warm regards. I would wish all the best for his profession and faultDissertationHighly Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Imines and an Application to a Formal Total Synthesis of Manzacidin cGradu Highly enantioselective 1,3 dipolar cyloaddition of azomethine imines and an application to a formal total synthesis of manzacidin c ce, assistance as well as knowledge exchange. I also thanks for the noteworthy time they spent with me. and that made every day well worth living. Hopefully, they all are always healthy and will do well in their life.I would like to thank: Prof. Yoshihito Hayashi. Dr. Keisuke Kawamoto for X-ray anal Highly enantioselective 1,3 dipolar cyloaddition of azomethine imines and an application to a formal total synthesis of manzacidin c ysis of this study. Prof. Masahito Segi. Prof. Yutaka Ukaji. Prof. Hajime Maeda. Prof. Takahiro Soeta. Prof. Taniyuki Funiyama. who are my dissertatioHighly enantioselective 1,3 dipolar cyloaddition of azomethine imines and an application to a formal total synthesis of manzacidin c
n Referees, have given me valuable comments and suggestions for completing my dissertation.I also thankful to all the Lecturers at Kanazawa UniversityDissertationHighly Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Imines and an Application to a Formal Total Synthesis of Manzacidin cGradu Highly enantioselective 1,3 dipolar cyloaddition of azomethine imines and an application to a formal total synthesis of manzacidin c e Student Association. Yukio Abe (Oto san). Mi Tetuo (Mi san) for sincere friendship, all their help and for concern as well as understanding.As the current of time. I greatly appreciate people who make my life extra special and give me soothing relief. I would send them my sweet feeling in deep res Highly enantioselective 1,3 dipolar cyloaddition of azomethine imines and an application to a formal total synthesis of manzacidin c pect for the way they did.I wish to thank Japan, a country has provided me a big lesson about realistic life. 1 study from such things I have experienHighly enantioselective 1,3 dipolar cyloaddition of azomethine imines and an application to a formal total synthesis of manzacidin c
ced. I hat would enrich my life on the way I wish to be.Family where the life begins and the love never ends, whenever I think of any of my successes;DissertationHighly Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Imines and an Application to a Formal Total Synthesis of Manzacidin cGradu Highly enantioselective 1,3 dipolar cyloaddition of azomethine imines and an application to a formal total synthesis of manzacidin c have given to me with their endless love. I spay for safety and happiness will stay beside them forever.It's time to be thanktill for all that godheads give us: bless US and keep US safe in their care.Kanazawa. February-2017TONG THI MINH THUTABLE OF CONTENTSABSTRACT................................. Highly enantioselective 1,3 dipolar cyloaddition of azomethine imines and an application to a formal total synthesis of manzacidin c ..........................................XVCHAPTER I: GENERAL INTRODUCTION.....................................................11.1.Manzacidin c - AnHighly enantioselective 1,3 dipolar cyloaddition of azomethine imines and an application to a formal total synthesis of manzacidin c
overview.....................................................11.1.1.Characterization, application and scientific reality.........................11.1DissertationHighly Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Imines and an Application to a Formal Total Synthesis of Manzacidin cGradu Highly enantioselective 1,3 dipolar cyloaddition of azomethine imines and an application to a formal total synthesis of manzacidin c r synthesis(Ohftine group)......................................................................31.1.2.2.Total synthesis of manzacidiu c using rhodium catalyst by stereospecific C-H bondoxidation (Dubois group).............................................................41.1.2.3.Total synthesis of m Highly enantioselective 1,3 dipolar cyloaddition of azomethine imines and an application to a formal total synthesis of manzacidin c anzacidin c using asymmetric aza-Mannich reaction (LanterDissertationHighly Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Imines and an Application to a Formal Total Synthesis of Manzacidin cGraduDissertationHighly Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Imines and an Application to a Formal Total Synthesis of Manzacidin cGraduGọi ngay
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