Publication | Open Access
The synthesis of desamido analogs of staurosporine, RK-286c, and TAN-1030a
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Citations
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References
1996
Year
EngineeringAlkene MetathesisDimethyl Acetal 16Desamido AnalogsOrganic ChemistryStereoselective SynthesisChemistryPharmacologySynthetic ChemistryEnantioselective SynthesisBiomolecular EngineeringNatural Product Synthesis
Ring expansion of dimethyl acetal 16 proceeds stereo- and regioselectively to 15 which is in turn converted to the desamido analogs of staurosporine, RK-286c, and TAN-1030a.
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