Publication | Closed Access
Phosphine-Catalyzed Sequential [2 +3] and [3 + 2] Annulation Domino Reaction of γ-Benzyl-Substituted Allenoates with α,β-Unsaturated Ketimines To Construct aza-Bicyclo[3,3,0]octane Derivatives
80
Citations
48
References
2014
Year
Chemical EngineeringExcellent DiastereoselectivityEngineeringHeterocyclicOrganic ChemistryCatalysisChemistryHeterocycle Chemistryγ-Benzyl-substituted AllenoatesEnantioselective SynthesisGood Yieldsβ-Unsaturated Ketimines
A novel phosphine-catalyzed sequential [2 + 3] and [3 + 2] annulation domino reaction of γ-benzyl-substituted allenoates has been developed. The reaction can proceed smoothly to produce the corresponding aza-bicyclo[3,3,0]octane derivatives in good yields and excellent diastereoselectivity (only one isomer).
| Year | Citations | |
|---|---|---|
Page 1
Page 1