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Synthesis of Muscothiazoles A and B: Critical Role of Methyl Group Substitution in RCM-Based Syntheses of Macrocycles
22
Citations
32
References
2003
Year
Single Methyl GroupRcm-based SynthesesEngineeringHeterocyclicNatural SciencesDiversity-oriented SynthesisCarbon ChainsOrganic ChemistrySubstrate 5Muscothiazoles AChemistryHeterocycle ChemistryMethyl Group SubstitutionPharmacologySynthetic ChemistryBiomolecular EngineeringNatural Product Synthesis
[reaction: see text] Muscothiazoles A (2b) and B (2c) have been prepared by two approaches that differ in the order of assembly of the rings. Comparative studies show that substitution of the carbon chains in substrate 5 or 12 (respective precursors to 13-membered and 14-membered rings by RCM), even by a single methyl group, can have a profound effect on increasing the efficiency of the macrocyclization.
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