Biomimetic cyclization of epoxide precursors of indole mono-, sesquiand diterpene alkaloids by lewis acids

Bioscience, Biotechnology and Biochemistry

Volumn 75, Issue 11, 2011, Pages 2213-2222

  Isaka, Tetsuya ^a   Hasegawa, Morifumi ^a,b   Toshima, Hiroaki ^a,b  

^a TOKYO UNIVERSITY OF AGRICULTURE AND TECHNOLOGY   (Japan)

^b IBARAKI UNIVERSITY   (Japan)

Author keywords

Biomimetic cyclization; Diterpene; Indole alkaloid; Monoterpene; Sesquiterpene

Indexed keywords

CATION INTERMEDIATES; CYCLIZATION PRODUCTS; DITERPENES; FARNESOL; GERANYLGERANIOL; INDOLE ALKALOID; LEWIS ACID; MONOTERPENES; POLYCYCLIC COMPOUNDS; PRODUCT FORMATION; SESQUITERPENES;

BIOMIMETICS; CHROMATOGRAPHY; METABOLITES; NITROGEN COMPOUNDS; OLEFINS;

CYCLIZATION;

DITERPENE; EPOXIDE; INDOLE ALKALOID; LEWIS ACID; POLYCYCLIC HYDROCARBON; SESQUITERPENE; TERPENE;

ARTICLE; BIOMIMETICS; CHEMICAL STRUCTURE; CHEMISTRY; CHROMATOGRAPHY; CYCLIZATION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; STEREOISOMERISM; SYNTHESIS;

BIOMIMETICS; CHROMATOGRAPHY; CYCLIZATION; DITERPENES; EPOXY COMPOUNDS; INDOLE ALKALOIDS; LEWIS ACIDS; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; MONOTERPENES; POLYCYCLIC COMPOUNDS; SESQUITERPENES; STEREOISOMERISM;

EID: 82155163694     PISSN: 09168451     EISSN: 13476947     Source Type: Journal    
DOI: 10.1271/bbb.110511     Document Type: Article

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