Diastereoselective Synthesis of Cularine Alkaloids via Enium Ions and an Easy Entry to Isoquinolines by Aza-Wittig Electrocyclic Ring Closure

Journal of Organic Chemistry

Volumn 69, Issue 9, 2004, Pages 2920-2928

  Rodrigues, J Augusto R ^a   Abramovitch, Rudolph A ^b   De Sousa, Joana D F ^a   Leiva, Genaro C ^a  

^a UNIVERSITY OF CAMPINAS   (Brazil)

^b CLEMSON UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ELECTROLYSIS; MOLECULAR STRUCTURE; REDUCTION; SODIUM COMPOUNDS; SYNTHESIS (CHEMICAL);

DIASTEREOSELECTIVE SYNTHESIS; METHYLATION; RING CLOSURES;

ORGANIC COMPOUNDS;

1',1,2,3 TETRAHYDRO[1]BENZOXEPINO[2,3,4 IJ]ISOQUINOLINE; 8 PHENYLMETHYL CHLOROACETATE; ALKALOID; CHLOROACETIC ACID; CLAVICULINE; CRASSIFOLINE; CULARICINE; CULARIMINE; CULARINE ALKALOID; HETEROCYCLIC COMPOUND; ION; ISOQUINOLINE DERIVATIVE; NATURAL PRODUCT; NITRENIUM; O NORCULARINE; OXENIUM; PLANT EXTRACT; SARCOCAPNIDINE; SARCOCAPNINE; SODIUM BOROHYDRIDE; UNCLASSIFIED DRUG;

ANALYTIC METHOD; ARTICLE; DIASTEREOISOMER; ELECTROCHEMICAL ANALYSIS; HORNER REACTION; METHYLATION; REDUCTION; RING CLOSING METATHESIS; STEREOCHEMISTRY; STRUCTURE ANALYSIS; SYNTHESIS;

ACETIC ACIDS; ALKALOIDS; CATIONS; CYCLIZATION; FREE RADICALS; ISOQUINOLINES; METHYLATION; MOLECULAR STRUCTURE; OXEPINS; OXIDATION-REDUCTION; STEREOISOMERISM; TEMPERATURE; TIME FACTORS;

EID: 2142659323     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo030287t     Document Type: Article

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