Publication | Closed Access
Synthetic Progress toward Azadirachtins. 2. Enantio- and Diastereoselective Synthesis of the Right-Wing Fragment of 11-<i>epi</i>-Azadirachtin I
16
Citations
50
References
2015
Year
EngineeringRight-wing FragmentOrganic ChemistryChemistryFuropyran MoietyDiastereoselective SynthesisSynthetic ProgressStereoselective SynthesisSilyl GlyoxylateCross-coupling ReactionBiochemistryDiversity-oriented SynthesisPharmacologyAsymmetric CatalysisNatural Product SynthesisEnantioselective SynthesisBiomolecular EngineeringAllylzinc BromideNatural Sciences
A stereoselective three-component coupling reaction of allylzinc bromide, silyl glyoxylate, and a β-lactone has been developed. This has been successfully applied to the enantio- and diastereoselective synthesis of the fully functionalized furopyran moiety of azadirachtins.
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