Andrea Guerrero‐Corella; Francisco Esteban; Manuel Iniesta; Ana Martín‐Somer; Mario Parra; Sergio Díaz‐Tendero; Alberto Fraile; Jose Alemán
文献索引:10.1002/anie.201800435
全文:HTML全文
An organocatalytic system is presented for the Michael addition of monoactivated glycine ketimine ylides with a bifunctional catalyst. The ketimine bears an ortho hydroxy group, which increases the acidity of the methylene hydrogen atoms and enhances the reactivity, thus allowing the synthesis of a large variety of α,γ‐diamino acid derivatives with excellent stereoselectivity.
Photo‐biocatalytic One‐Pot Cascades for the Enantioselective...
2018-04-14 [10.1002/anie.201802135] |
Synthesis of (bis)Silicon Complexes of [38], [37], and [36]O...
2018-04-14 [10.1002/anie.201801986] |
Samarium Polystibides Derived from Highly Activated Nanoscal...
2018-04-14 [10.1002/anie.201802250] |
A Monoaryllead Trichloride that Resists Reductive Eliminatio...
2018-04-14 [10.1002/anie.201712944] |
On the Origin of the Distinctly Different Reactivity of Ruth...
2018-04-14 [10.1002/anie.201800173] |
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 © 2024 ChemSrc All Rights Reserved