Helvetica Chimica Acta · 1987 · 24 citations · 15 references
BiosynthesisBioorganic ChemistryRh‐catalyzed ReactionBiochemistryEngineeringNatural SciencesDiversity-oriented SynthesisEthyl DiazopyruvateOrganic ChemistryOrganometallic CatalysisCatalysisChemistryHeterocycle ChemistryNatural Product SynthesisSynthetic ChemistryEnantioselective SynthesisFunctional‐group TransformationNatural Tropone
Abstract The Rh‐catalyzed reaction of 1,3‐butadiene with ethyl 3‐diazopyruvate leads, inter alia , to a dihydro‐oxepinecarboxylate whose oxidation and functinal‐group manipulation produce salicylates. Wittig reactions on the acylcyclopropane accompanying the dihydrooxepine yields acrylates whose pyrolyses afford cycloheptadiene‐carboxylates. Oxidation and functional‐group transformation produces the natural tropone, nezukone.
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Hidemasa Takaya, Yoshihiro Hayakawa, S. MAKINO et al. · Journal of the American Chemical Society · 1978 · 63 citations
E. WENKERT · Heterocycles · 1980 · 44 citations · Full text
Derivative (Chemistry), Engineering, Linear Chain Compound +6