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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D217-16
filingDate 2018-12-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_35e501129b7c9a0fde520ab4b08dbe2f
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publicationDate 2019-04-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-109608395-A
titleOfInvention A new green synthesis method for efficient synthesis of isoquinoline derivatives by transition metal-catalyzed C-H activation/cyclization reaction
abstract The invention relates to a C-H activation/cyclization reaction using water as a solvent, sulfur ylide as a carbene donor, and transition metal catalysis to efficiently form a C-C bond on an aromatic (hetero) ring, and cyclically synthesize isoquinoline derivatives A new method for green synthesis of substances. Compared with the traditional method, the method has easy-to-obtain raw materials, simple steps, avoids the use of toxic organic solvents, is a mild, fast, simple, effective and environmentally friendly method for preparing isoquinoline parent rings, and has broad application. prospect.
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