Invention Grant
US08372985B2 Process of making α-aminooxyketone/α-aminooxyaldehyde and α-hydroxyketone/α-hydroxyaldehyde compounds and a process of making reaction products from cyclic α, β-unsaturated ketone substrates and nitroso substrates
有权
制备α-氨基氧基酮/α-氨基氧醛和α-羟基酮/α-羟基醛化合物的方法和由环状α,β-不饱和酮底物和亚硝基底物制备反应产物的方法
- Patent Title: Process of making α-aminooxyketone/α-aminooxyaldehyde and α-hydroxyketone/α-hydroxyaldehyde compounds and a process of making reaction products from cyclic α, β-unsaturated ketone substrates and nitroso substrates
- Patent Title (中): 制备α-氨基氧基酮/α-氨基氧醛和α-羟基酮/α-羟基醛化合物的方法和由环状α,β-不饱和酮底物和亚硝基底物制备反应产物的方法
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Application No.: US13566587Application Date: 2012-08-03
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Publication No.: US08372985B2Publication Date: 2013-02-12
- Inventor: Norie Momiyama , Hiromi Torii , Susumu Saito , Hisashi Yamamoto , Yuhei Yamamoto
- Applicant: Norie Momiyama , Hiromi Torii , Susumu Saito , Hisashi Yamamoto , Yuhei Yamamoto
- Applicant Address: JP Saitama
- Assignee: Japan Science and Technology Agency
- Current Assignee: Japan Science and Technology Agency
- Current Assignee Address: JP Saitama
- Agency: Frommer Lawrence & Haug LLP
- Priority: JP2004-044540 20040220
- Main IPC: C07D257/04
- IPC: C07D257/04

Abstract:
The present invention is directed to a process of making α-aminooxyketone and α-hydroxyketone compounds. The synthetic pathway generally involves reacting an aldehyde or ketone substrate and a nitroso substrate in the presence of a catalyst of the formula (IV): wherein Xa-Xc represent independently nitrogen, carbon, oxygen or sulfur and Z represents a 4 to 10-membered ring with or without a substituent and optionally a further step to convert the α-aminooxyketone compound formed to the α-hydroxyketone compound. The present invention results in α-aminooxyketone and α-hydroxyketone compounds with high enantioselectivity and high purity. The present invention is also directed to a catalytic asymmetric O-nitroso Aldol/Michael reaction. The substrates of this reaction are generally cyclic α,β-unsaturated ketone substrate and a nitroso substrate. This methodology generally involves reacting the cyclic α,β-unsaturated ketone substrate and the nitroso substrate in the presence of a proline-based catalyst, to provide a heterocyclic product.
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