A new synthetic route to 2-methyl-3-(aryl or alkyl)-1-oxo-1,2-dihydroisoquinolines via an intramolecular Wittig reaction

Tetrahedron

Volumn 48, Issue 19, 1992, Pages 3857-3866

  Couture, Axel ^a   Cornet, Hélène ^a   Grandclaudon, Pierre ^a  

^a CNRS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ISOQUINOLINE DERIVATIVE;

ARTICLE; MASS SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; SYNTHESIS;

EID: 0026606777     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(01)88466-0     Document Type: Article

References (31)

1. A Convenient Synthesis ofNMethyl-1(2H)-isoquinolones
2. Reactions of Glutaconic and Homophthalic Anhydrides with Imidates, Imidoyl Chlorides, and 1-Chloroisoquinoline
3. Photochemistry of the N-Oxides of Azanaphthalene and Their Substituted Derivatives
4. Enamide Photochemistry. A Convenient Synthesis of 3-Aryl-1-oxotetrahydro- and dihydro-Isoquinolines (Isocarbostyrils)
5. Selected topics of the wittig reaction in the synthesis of natural products
6. Industrial applications of the wittig reaction
7. The Wittig Reaction : 30 Years Later
8. One-Pot Synthesis of 5,6-Dihydro-8H-dibenzo[a,g]quinolizine-8-ones and Related Isoquinolines; A New Synthesis of Xylopinine