2009
DOI: 10.1002/chin.200924121
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ChemInform Abstract: 2‐Oxazol‐5‐ylethanones by Consecutive Three‐Component Amidation—Coupling—Cycloisomerization (ACCI) Sequence.

Abstract: Oxazole derivatives R 0220 2-Oxazol-5-ylethanones by Consecutive Three-Component Amidation-Coupling-Cycloisomerization (ACCI) Sequence. -(MERKUL, E.; GROTKOPP, O.; MUELLER*, T. J. J.; Synthesis 2009, 3, 502-507; Inst. Org. Chem. Makromol. Chem., Heinrich-Heine-Univ., D-40225 Duesseldorf, Germany; Eng.) -Mais 24-121

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“…The oxazole and isoxazole moieties are common heterocyclic motifs identified in many natural products and biologically active compounds. An efficient three steps synthesis of 2,5-polyfunctionalized oxazole derivatives was developed by Müller's group [91,92] starting from acyl chlorides and propargyl amine. The first reaction consisted in an amidation of the acid chloride promoted by Et 3 N, followed by in situ Sonogashira cross-coupling of the generated alkynyl amide with another equivalent of RCOCl.…”
Section: Synthesis Of No-heterocycles By Acyl Sonogashira Reactionsmentioning
confidence: 99%
“…The oxazole and isoxazole moieties are common heterocyclic motifs identified in many natural products and biologically active compounds. An efficient three steps synthesis of 2,5-polyfunctionalized oxazole derivatives was developed by Müller's group [91,92] starting from acyl chlorides and propargyl amine. The first reaction consisted in an amidation of the acid chloride promoted by Et 3 N, followed by in situ Sonogashira cross-coupling of the generated alkynyl amide with another equivalent of RCOCl.…”
Section: Synthesis Of No-heterocycles By Acyl Sonogashira Reactionsmentioning
confidence: 99%