@article{MTMT:1366571, title = {Convenient Synthesis of 1,2,3,4-Tetrahydroisoquinoline-1-carboxylic Acid Derivatives via Isocyanide-Based, Three-Component Reactions}, url = {https://m2.mtmt.hu/api/publication/1366571}, author = {Schuster, Ildikó and Lázár, László and Fülöp, Ferenc}, doi = {10.1080/00397910903277920}, journal-iso = {SYNTHETIC COMMUN}, journal = {SYNTHETIC COMMUNICATIONS}, volume = {40}, unique-id = {1366571}, issn = {0039-7911}, abstract = {The three-component reactions of 3,4-dihydroisoquinolines, isocyanides, and benzyl chloroformate furnished 2-benzyloxycarbonyl-1,2,3,4-tetrahydroisoquinoline-1-carboxamides in moderate to good yields. Hydrogenolysis or selective hydrolysis of the benzyloxycarbonyl group provided 1,2,3,4-tetrahydroisoquinoline-1-carboxamides, further hydrolysis of which resulted in the corresponding 1,2,3,4-tetrahydroisoquinoline-1-carboxylic acids.}, keywords = {WATER; Isoquinolines; ISOQUINOLINE; TETRAHYDROISOQUINOLINE; MULTICOMPONENT REACTIONS; ISOCYANIDES; ugi reactions; SALTS; STRONG CH-ACIDS; -Amino acids}, year = {2010}, eissn = {1532-2432}, pages = {2488-2498}, orcid-numbers = {Lázár, László/0000-0002-2135-8496; Fülöp, Ferenc/0000-0003-1066-5287} }