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The synthesis was based by using some elementary organic chemistry reactions. The products were characterized by NMR dates and MS analysis."},"dsDescriptionDate":{"typeName":"dsDescriptionDate","multiple":false,"typeClass":"primitive","value":"2025-09-15"}}]},{"typeName":"subject","multiple":true,"typeClass":"controlledVocabulary","value":["Chemistry"]},{"typeName":"keyword","multiple":true,"typeClass":"compound","value":[{"keywordValue":{"typeName":"keywordValue","multiple":false,"typeClass":"primitive","value":"tetrahydroisoquinoline and Piperidine Scaffolds by Oxidative Ring Opening/Ring Closing  NMR, MS, beta- amino acids, heterocycles"}}]},{"typeName":"publication","multiple":true,"typeClass":"compound","value":[{"publicationCitation":{"typeName":"publicationCitation","multiple":false,"typeClass":"primitive","value":"Semghouli A, Drahos L, Han J, Kiss L, Nonn M. Selective Synthesis of Tetrahydroisoquinoline and Piperidine Scaffolds by Oxidative Ring Opening/Ring Closing Protocols of Substituted Indenes and Cyclopentenes. ChemistryOpen. 2025 May;14(5):e202400475. doi: 10.1002/open.202400475. Epub 2024 Dec 27. 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