20 research outputs found
A Metal-Free Tandem C–C/C–O Bond Formation Approach to Diversely Functionalized Tetrasubstituted Furans
ChemInform Abstract: A Metal‐Free Tandem C—C/C—O Bond Formation Approach to Diversely Functionalized Tetrasubstituted Furans.
Novel [4 + 2]-Benzannulation To Access Substituted Benzenes and Polycyclic Aromatic and Benzene-Fused Heteroaromatic Compounds
ChemInform Abstract: Organocatalyzed Intramolecular Michael Addition of Morita—Baylis—Hillman Adducts of β‐Arylnitroethylenes: An Entry to 3‐Aryl‐4‐nitrocyclohexanones.
ChemInform Abstract: Tandem Allylic Substitution—5‐exo‐dig‐Carbocyclization: A [4 + 1]‐Annulation Approach to Arylidene Cyclopentenes from MBH‐Acetates of Acetylenic Aldehydes.
ChemInform Abstract: Novel [4 + 2]‐Benzannulation to Access Substituted Benzenes and Polycyclic Aromatic and Benzene‐Fused Heteroaromatic Compounds.
A Metal-Free Tandem C–C/C–O Bond Formation Approach to Diversely Functionalized Tetrasubstituted Furans
A novel and efficient method for
the synthesis of diversely functionalized
furans is developed via DBU-mediated tandem Michael addition/5-exo-dig-cycloisomerization of enynes and keto-methylenes.
This [3 + 2]-annulation is operationally simple under metal-free reaction
conditions with 100% atom economy and broad substrate scope
