Rearrangements and cyclizations of 2-chloropropenyl-appended indolo[2,3- a]quinolizidine derivatives

European Journal of Organic Chemistry

Volumn , Issue 12, 1999, Pages 3429-3432

  Aït Mohand, Samia ^a   Noé, Eric ^a   Hénin, Jacques ^a   Laronze, Jean Yves ^a  

^a UNIVERSITÉ DE REIMS CHAMPAGNE ARDENNE   (France)

Author keywords

Allylic rearrangement; Apovincamine; Cyclizations; Indoloquinolizidine

Indexed keywords

INDOLOQUINOLINE DERIVATIVE; KETONE; VINCAMINE;

ARTICLE; CHEMICAL MODIFICATION; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLIZATION;

EID: 0141512471     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1099-0690(199912)1999:12<3429::aid-ejoc3429>3.0.co;2-r     Document Type: Article

References (8)

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2. 1H NMR spectroscopy (no splitting). It is represented by both its ketonic and enolic forms. The structure was well established by extensive COSY, HMBC and HMQC NMR measurements.
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