Publication | Closed Access
The First Total Synthesis of (±)-Napyradiomycin A1
26
Citations
7
References
2002
Year
Medicinal ChemistryBiochemistryNatural SciencesChlorine AtomsDiversity-oriented SynthesisFirst Total SynthesisOrganic ChemistrySynthetic ChemistryStereoselective SynthesisHeterocycle ChemistryPharmacologySide Chain-Napyradiomycin A1Natural Product Synthesis
Abstract (±)-Napyradiomycin A1 has been stereoselectively synthesized through a tandem Michael-Dieckmann type reaction and the introduction of a side chain and two chlorine atoms onto the pyranonaphthoquinone core.
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