Načítá se...
Formation of Non-Natural α,α-Disubstituted Amino Esters via Catalytic Michael Addition
The enolate monoanion of amino esters is explored, and the first catalytic Michael addition of α-amino esters is demonstrated. These studies indicate that the acidity of the αC–H is the primary factor determining reactivity. Thus, polyfluorophenylglycine amino esters yield novel α-amino esters in th...
Uloženo v:
| Vydáno v: | Org Lett |
|---|---|
| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2018
|
| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6581451/ https://ncbi.nlm.nih.gov/pubmed/30387616 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acs.orglett.8b03161 |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!
|