| Course title | |||||
| 有機反応化学特論 [Advanced Organic Reaction] | |||||
| Course category | courses for master's programs | Requirement | Credit | 2 | |
| Department | Year | ～ | Semester | 1st | |
| Course type | 1st | Course code | 1060201 | ||
| Instructor(s) | |||||
| 森 啓二, 平野 雅文 [MORI Keiji, HIRANO Masafumi] | |||||
| Facility affiliation | Faculty of Engineering | Office | Email address | ||
| Course description |
|
All organic compounds possesses three dimentional structure because main unit, carbon, can have four substituents around it. Since the properties on molecule is dramatically changed by the three dimentional structure, the stereoselective synthesis of organic acrchitecture is major topic in synthetic organic chemistry. In this lecture, I want to explain the details about stereocontrolled synthesis of various important class of organic molecules, and the way of thinking of the reaction mechanism using curved arrow. 【classcode】 z42455h |
| Expected Learning |
|
Understanding the stereoselective reaction, which is indispensable knowledge in modern synthetic organic synthesis Corresponding criteria in the Diploma Policy: See the Curriculum maps. |
| Course schedule |
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1st Lecture: introduction 2nd Lecture: Fundamental information on asymmetric synthesis 3rd Lecture: DIels-Alder reaction 1 4th Lecture: DIels-Alder reaction 2 5th Lecture: Aldol reaction 1 6th Lecture: Aldol reaction 2 7th Lecture: Summarization of the previous classes (from 1st to 6th), Midterm exam 8th Lecture: Stereoselective synthesis of olefins 1 9th Lecture: Stereoselective synthesis of olefins 1 10th Lecture: Pericyclic reaction 1 11th Lecture: Pericyclic reaction 2 12th Lecture: Asymmetric synthesis involving kinetic resolution 1 13th Lecture: Asymmetric synthesis involving kinetic resolution 2 14th Lecture: Method for controlling of various special asymmetric information 15th Lecture: Summarization of the previous classes (from 1th to 14th), Term-end examination |
| Prerequisites |
| Although teacher consider about students who are not familiar with organic chemistry, the fundamental knowledge, which are taught in bachelor degree, are indispensable to understand the contents. |
| Required Text(s) and Materials |
| nothing |
| References |
| Organic Chemistry for lecture in graduate course edited by R. Noyorei, M. Shibasaki, K. Suzuki, K. Tamao, K. Nakasuji, K. Narasaka, Tokyo Kagaku Dojin Ltd. Co. |
| Assessment/Grading |
|
The method of a scholastic evaluation: Consider it as attendance + homework (50%), a midterm exam (25%), and a term-end examination (25%), and judge in these sum totals. Grade will be given according to the following criteria by comprehensive evaluation: S: 90 points or more, A: 80 or more and less than 90 points, B: 70 or more and less than 80 points, C: 60 or more and less than 70 points. Grade distribution in 2020: S: 17%, A: 33%, B: 33%, C: 17% (The equivalent distribution is not warranted.) |
| Message from instructor(s) |
| Become a expert on rationalizing the stereochemistry, which is weak point for most of the student |
| Course keywords |
| stereoselective synthesis, catalytic reaction, asymmetric reaction |
| Office hours |
| Remarks 1 |
| Remarks 2 |
| Related URL |
| Lecture Language |
| Japanese |
| Language Subject |
| Last update |
| 2/18/2022 6:34:48 PM |