Publication | Closed Access
Total Synthesis of Spirotryprostatins through Organomediated Intramolecular Umpolung Cyclization
42
Citations
69
References
2019
Year
Molecular PharmacologyDiversity Oriented SynthesisNatural AlkaloidsBiochemistryUmpolung CyclizationMedicineNatural SciencesDiversity-oriented SynthesisTotal SynthesisOrganic ChemistryPeptide SciencePharmacologyGeneral AmidesPharmaceutical ChemistrySynthetic ChemistryBiomolecular EngineeringDrug DiscoveryNatural Product Synthesis
Cyclodipeptide 2,5-diketopiperazines (DKP) are privileged structural units present in drugs and natural alkaloids. This work reports a new method for the synthesis of biologically important DKP scaffolds based on an intramolecular nucleophilic α-addition of general amides towards an alkynamide system. The utility of this umpolung cyclization mediated by trimethyl phosphine and l-glutamic acid is highlighted by its application to the concise total syntheses of 6-methoxyspirotryprostatin B (the first total synthesis), spirotryprostatin A, and spirotryprostatin B.
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2002 | 687 | |
2000 | 490 | |
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2000 | 431 | |
2007 | 387 | |
2011 | 366 | |
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