| Project/Area Number |
12557198
|
|---|
| Research Category |
Grant-in-Aid for Scientific Research (B)
|
| Allocation Type | Single-year Grants |
|---|
| Section | 展開研究 |
|---|
| Research Field |
Chemical pharmacy
|
|---|
| Research Institution | TOHOKU UNIVERSITY |
|---|
Principal Investigator |
KONDO Yoshinori TOHOKU UNIVERSITY, GRADUATE SCHOOL OF PHARMCEUTICAL SCIENCES, PROFESSOR, 大学院・薬学研究科, 教授 (90162122)
|
|---|
| Project Period (FY) |
2000 – 2001
|
| Project Status |
Completed (Fiscal Year 2001)
|
| Budget Amount *help |
¥12,500,000 (Direct Cost: ¥12,500,000)
Fiscal Year 2001: ¥3,000,000 (Direct Cost: ¥3,000,000)
Fiscal Year 2000: ¥9,500,000 (Direct Cost: ¥9,500,000)
|
|---|
| Keywords | ORGANOMETALLICS / SOLID PHASE SYNTHESIS / CHEMOSELECTIVE METALATION / HETEROCYCLIC COMPOUNDS / INDOLE DERIVATIVES / POLYMER SUPPORT / PALLADIUM CATALYST / CARBON-CARBON BOND FORMATION / 複素環化合物 / 固相反応 / メタル化 / インドール / 炭素-炭素結合生成 / アート錯体 / ポリアー担体 |
|---|
| Research Abstract |
Solid phase synthesis of heterocyclic compounds was investigated using organometallic reagents. Among them, nitrogen heteroaromatics such as indoles, pyridines were chemoselectively metalated using various organometallic reagents and it was found that mesityllithium works as a chemoselective deprotonating agent for solid phase metalation. Scope and limitation was disclosed for the solid phase deprotonation and the reactions with various electrophiles were also examined. Stabilization of the intermediary immobilized oragnometallic species was examined using spectroscopic measurements. As an application of the metalation, the combination with palladium catalyzed reactions was studied and new indole cyclizations using intramolecular palladium catalyzed coupling reaction were also developed. Approaches for high throughput synthesis were investigated using a automated synthesizer and the usefulness of the polymer supported chemistry was demonstrated.
|
