Organic Letters · 2002 · 43 citations · 13 references
PharmacyChemistryMedicinal ChemistryCarbohydrate ChemistryDrug DiscoverySynthetic Medicinal ChemistryCarbohydrate SynthesisLead Compound DesignLigand-based DesignMacrocycle SynthesisNatural Product-based Drug DesignRetrosynthetic AnalysisAldol ReactionBioactive Molecule SynthesisChemical Synthesis Of AnaloguesGlycan-inspired Drug DesignMedicinal Chemistry ApplicationsMode Of Action StudiesModular DesignNatural Product Total Synthesis
[reaction: see text] A highly convergent synthesis of the angiogenesis inhibitor luminacin D has been achieved in 13 linear steps (19 steps total, 5.3% overall yield) utilizing a samarium(II) iodide-mediated mixed tandem aldol/Evans-Tishchenko reaction to construct the carbohydrate precursor. The modular synthetic design will allow derivatization at key positions necessary for biochemical mode of action studies.
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Jue‐Liang Hsu, Jim‐Min Fang · The Journal of Organic Chemistry · 2001 · 65 citations
UCS15A, a non-kinase inhibitor of Src signal transduction
Sreenath V. Sharma, Chitose Oneyama, Yoshinori Yamashita et al. · Oncogene · 2001 · 58 citations