Hetero-diels-alder reactions of α-methoxymethylene substituted 1.3-dicarbonyl compounds with enol and enediol ethers-Science-Chemical Encyclopedia-lookchem

Hetero-diels-alder reactions of α-methoxymethylene substituted 1.3-dicarbonyl compounds with enol and enediol ethers
Add time:09/01/2019 Source:sciencedirect.com

The inverse electron demand hetero-Diels-Alder reaction of methoxymethylene substituted 1.3-dicarbonyl compounds with enol ethers and enediol ethers results in the selective formation of 3.4-dihydro-2H-pyrans. These adducts with a high density of functional groups are versatile intermediates for natural product syntheses.

We also recommend Trading Suppliers and Manufacturers of 5-(METHOXYMETHYLENE)-2,2-DIMETHYL-1,3-DIOXANE-4,6-DIONE (cas 15568-85-1). Pls Click Website Link as below: cas 15568-85-1 suppliers

Prev:The vibrational and NMR spectra, conformations and ab initio calculations of 3-methoxymethylene-2,4-pentanedione
Next: The vibrational and NMR spectra, conformations and ab initio calculations of methoxymethylene- and 1-methoxyethylidene- propanedinitrile)

Click to view details

Encyclopedia