A new synthetic approach to 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid (Tic) derivatives via a [2 + 2 + 2] cycloaddition reaction

Bioorganic and Medicinal Chemistry Letters

Volumn 10, Issue 13, 2000, Pages 1413-1415

  Kotha, Sambasivarao ^a   Sreenivasachary, Nampally ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY BOMBAY   (India)

Author keywords

[No Author keywords available]

Indexed keywords

CARBOXYLIC ACID DERIVATIVE;

ARTICLE; CATALYSIS; DRUG INHIBITION; DRUG SYNTHESIS; MOLECULAR DYNAMICS; REACTION ANALYSIS; STRUCTURE ANALYSIS;

ALKYNES; CATALYSIS; CYCLIZATION; DRUG DESIGN; ISOQUINOLINES;

EID: 0034601143     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(00)00259-6     Document Type: Article

References (28)

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28. 13C NMR data for selected compounds: (1) δ 13.8, 20.7, 21.4, 34.3, 58.0, 61.7, 71.5, 73.0, 78.3, 78.9, 127.7, 129.3, 136.7, 143.7, 169.0. (5) δ 0.03, 14.3, 21.1, 21.9, 35.8, 58.7, 62.1, 71.7, 79.7, 99.3, 100.2, 128.3, 129.7, 137.6, 143.9, 169.4. (6) δ 13.7, 21.5, 31.5, 44.0, 53.5, 61.3, 63.5, 127.2, 127.3, 129.5, 129.9, 130.3, 130.6, 135.9, 137.9, 143.6, 170.1. (7) δ 13.8, 21.5, 31.7, 44.1, 53.8, 61.3, 126.5, 127.4, 127.8, 128.1, 129.5, 129.7, 130.8, 139.1, 140.8, 143.5, 170.2. (11) δ 1.9, 14.0, 21.5, 31.9, 44.2, 53.7, 61.1, 127.4, 129.4, 130.1, 130.9, 133.0, 135.7, 136.5, 143.2, 144.1, 170.1. (12) δ 14.0, 21.6, 31.9, 44.1, 52.5, 53.0, 61.2, 127.1, 127.5, 129.5, 130.5, 130.6, 134.3, 134.9, 136.2, 143.4, 167.0, 169.2, 169.4.