Establishment of Breakthrough on Unactivated Alkane C-H Bond Amination
Project/Area Number |
24659006
|
Research Category |
Grant-in-Aid for Challenging Exploratory Research
|
Allocation Type | Multi-year Fund |
Research Field |
Chemical pharmacy
|
Research Institution | The University of Tokushima |
Principal Investigator |
OCHIAI Masahito 徳島大学, 大学院・ヘルスバイオサイエンス研究部, 教授 (50127065)
|
Project Period (FY) |
2012
|
Project Status |
Completed (Fiscal Year 2012)
|
Budget Amount *help |
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2012: ¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
|
Keywords | 有機化学 / CHアミノ化反応 / ナイトレノイド / 臭素 / 超原子価 / アルカン |
Research Abstract |
Our project involves a development of new research field “chemistry of hypervalent bromane”. We have developed a new methodology for direct regioselective alkane C-H amination, which involves in situ generation of iminobromane. Iminobromane generated from diacyloxybromane by the reaction with triflylamide in alkane as a solvent undergoes alkane C-H amination. Excellent regioselectivity as well as stereoselectivity were observed in the reaction.
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Report
(2 results)
Research Products
(23 results)