Publication | Closed Access
Asymmetric hydrogen transfer protocol for enantiocontrolled synthesis of (−)-chokol G
18
Citations
11
References
1998
Year
Key StepBiosynthesis-Chokol GEngineeringBiochemistryNatural SciencesBiocatalysisEpichloe TyphiaNatural Product BiosynthesisOrganic ChemistryStereoselective SynthesisChemistryNatural Product SynthesisAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular EngineeringEnantiocontrolled Synthesis
An enantiocontrolled route to the (–)-chokol G, a fungitoxic metabolite from stromata of Epichloe typhia, has been devised by employing a RuII-catalyzed asymmetric hydrogen transfer reaction as the key step.
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