Publication | Closed Access
Total Synthesis of Aplykurodinone-1
25
Citations
53
References
2014
Year
Combinatorial ChemistryBioorganic ChemistryEngineeringBiochemistryGroup ChemistryNatural SciencesHeterocyclicDiversity-oriented SynthesisTotal SynthesisOrganic ChemistryOrganometallic CatalysisChemistryHeterocycle ChemistryNatural Product SynthesisSynthetic ChemistryUnique Smi2Biomolecular EngineeringConcise Total Synthesis
The concise total synthesis of aplykurodinone-1 with an unusual cis-fused hydrindane moiety has been accomplished without the need for any protecting group chemistry using a unique SmI2 mediated reductive cascade cyclization reaction and a direct cuprate mediated 1,4-addition. This work represents the first example of the use of a SmI2-mediated intramolecular cascade cyclization reaction between "halide, alkene and aldehyde" groups.
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