Oxiranes in the Ritter reaction. Synthesis of 6,7- and 5,8-dimethoxy-3,3-dialkyl-3,4-dihydroisoquinolines by a tandem alkylation-cyclization reaction

Chemistry of Heterocyclic Compounds

Volumn 37, Issue 4, 2001, Pages 444-452

  Glushkov, V A ^a   Shurov, S N ^b   Maiorova, O A ^a   Postanogova, G A ^a   Feshina, E V ^a   Shklyaev, Yu V ^a  

^a INSTITUTE OF TECHNICAL CHEMISTRY   (Russian Federation)

^b PERM STATE UNIVERSITY   (Russian Federation)

Author keywords

1,4 Dimethoxybenzene; Alkylation; AM1 method; Cyclization; Isoquinoline; Nitriles; Oxiranes; Quantum chemical calculations; Ritter reaction; Veratrolel

Indexed keywords

1,4 DIMETHOXYBENZENE; 3,3 TETRAMETHYLENE 3,4 DIHYDROISOQUINOLINE; 5,8 DIMETHOXY 3,3 DIMETHYL 3,4 DIHYDROISOQUINOLINE; 6,7 DIMETHOXY 3,3 DIMETHYL 3,4 DIHYDROISOQUINOLINE; BENZENE DERIVATIVE; CYANOACETIC ACID ESTER; CYCLOHEXANE OXIDE; ESTER; ETHYLENE OXIDE DERIVATIVE; ISOBUTYLENE; ISOQUINOLINE DERIVATIVE; NITRILE; TETRAHYDROISOQUINOLYLIDENEACETIC ACID; UNCLASSIFIED DRUG; VERATROLE;

ALKYLATION; ARTICLE; CYCLIZATION; INFRARED SPECTROSCOPY; PROTON NUCLEAR MAGNETIC RESONANCE; QUANTUM CHEMISTRY; REACTION ANALYSIS; SYNTHESIS;

EID: 0035322698     PISSN: 00093122     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1017643703041     Document Type: Article

References (18)