A new route to trans-2,6-disubstituted piperidine-related alkaloids using a novel C2-symmetric 2,6-diallylpiperidine carboxylic acid methyl ester

Organic and Biomolecular Chemistry

Volumn 4, Issue 8, 2006, Pages 1587-1595

  Takahata, Hiroki ^a   Saito, Yukako ^a   Ichinose, Motohiro ^b  

^a TOHOKU PHARMACEUTICAL UNIVERSITY   (Japan)

^b UNIVERSITY OF TOYAMA   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDES; CARBOXYLIC ACIDS; ESTERS; SYNTHESIS (CHEMICAL);

C2-SYMMETRIC 2,6-DIALLYLPIPERIDINE CARBOXYLIC ACID METHYL ESTER; IODOCARBAMATION; TRANS-2,6-DISUBSTITUTED PIPERIDINE-RELATED ALKALOIDS;

AROMATIC COMPOUNDS;

2,6 DIALLYLPIPERIDINE CARBOXYLIC ACID METHYL ESTER; 2,6-DIALLYLPIPERIDINE CARBOXYLIC ACID METHYL ESTER; ALKALOID; ESTER; PIPERIDINE DERIVATIVE;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; SYNTHESIS;

ALKALOIDS; ESTERS; MOLECULAR STRUCTURE; PIPERIDINES;

EID: 33744481773     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b601489e     Document Type: Article

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