Niels Borlinghaus, Sebastian Gergel, Bettina M. Nestl
文献索引:10.1021/acscatal.8b00291
全文:HTML全文
Given the widespread importance of piperazines as building blocks for the production of pharmaceuticals, an efficient and selective synthesis is highly desirable. Here we show the direct synthesis of piperazines from 1,2-dicarbonyl and 1,2-diamine substrates using the R-selective imine reductase from Myxococcus stipitatus as biocatalyst. Various N- and C-substituted piperazines with high activity and excellent enantioselectivity were obtained under mild reaction conditions reaching up to 8.1 g per liter.
|
Iron-Catalyzed Direct Olefin Diazidation via Peroxyester Act...
2018-04-19 [10.1021/acscatal.8b00821] |
|
Catalytic Dehydrogenation of (Di)Amine-Boranes with a Geomet...
2018-04-18 [10.1021/acscatal.8b00152] |
|
Well-Defined β-Diketiminatocobalt(II) Complexes for Alkene C...
2018-04-18 [10.1021/acscatal.8b00631] |
|
Isoprene Regioblock Copolymerization: Switching the Regiosel...
2018-04-18 [10.1021/acscatal.8b00600] |
|
Low-Energy Electrocatalytic CO2 Reduction in Water over Mn-C...
2018-04-18 [10.1021/acscatal.8b01068] |
首页 |
期刊大全 |
MSDS查询 |
化工产品分类 |
生物活性化合物 |
关于我们 |
免责声明:知识产权问题请联系 service1@chemsrc.com
Copyright © 2026 ChemSrc All Rights Reserved