Yumi Murata; Takashi Nishikata
文献索引:10.1002/chem.201801065
全文:HTML全文
In this work, we established a general protocol to synthesize single α‐tert‐alkylated acetaldehydes via Cu‐catalyzed hydroxyalkylation of enamides in aqueous solutions. The yields of the products were very high and there was excellent functional group compatibility. Our reaction allows easy access to highly functionalized acetaldehydes that can be used to synthesize further useful compounds including spirocycles. The control experiments revealed that this reaction includes hydroxyalkylation processes via radical reactions.
|
Subnaphthalocyanines as Electron Acceptors in Polymer Solar ...
2018-04-10 [10.1002/chem.201800596] |
|
Formal Lossen Rearrangement/[3+2] Annulation Cascade Catalyz...
2018-04-10 [10.1002/chem.201801125] |
|
A Highly Sensitive Fluorogenic Probe for Imaging Glycoprotei...
2018-04-10 [10.1002/chem.201800790] |
|
Improvement of Photodynamic Activity of Lipid–Membrane‐Incor...
2018-04-06 [10.1002/chem.201800674] |
|
Ordered Mesoporous Titania/Carbon Hybrid Monoliths for Lithi...
2018-04-06 [10.1002/chem.201801099] |