Literature DB >> 21384318

Simple indole alkaloids from the neotropical rutaceous tree Raputia simulans.

Konstantina Vougogiannopoulou1, Nikolas Fokialakis, Nektarios Aligiannis, Charles Cantrell, Alexios-Leandros Skaltsounis.   

Abstract

The genus Raputia Aubl. comprises 10 neotropical species of the family Rutaceae belonging to the subtribe Cuspariinae. We report herein the investigation of the dichloromethane extract of the stem bark of R. simulans, which has led to the isolation of indole type alkaloids. The isolation procedure was performed by fast centrifugal partition chromatography (FCPC) and adsorption chromatography and afforded 11 isolates: indole-5-carbaldehyde (1), 7-prenylindole (2), 5-prenylindole (3), verticillatine B (4), 5-(but-3'-en-2'-one)indole (5), 5-(2'-methylbut-3'-en-1'-ol)indole (6), 5-[methyl-4'-(2'-methyl-4-oxobutanoate)]indole (7), 5-[4-(methyl)furan-2-yl]indole ( 8), 5-[4-(methoxymethyl)furan-2-yl]indole (9), 5-[5'-(3-methylfuran-2'(5' H)-one)]indole (10), and 5-(4'-methyl-2',5'-dihydrofuran-2'-yl)indole (11). Metabolites 5- 11 were isolated for the first time and bear uncommon substituents on position 5 of the indole moiety. © Georg Thieme Verlag KG Stuttgart · New York.

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Year:  2011        PMID: 21384318     DOI: 10.1055/s-0030-1270850

Source DB:  PubMed          Journal:  Planta Med        ISSN: 0032-0943            Impact factor:   3.352


  2 in total

1.  Synthesis of (-)-Dihydroraputindole D by Enantioselective Benzoylation of a 1,3-Diol Intermediate.

Authors:  Marvin Fresia; Mario Kock; Thomas Lindel
Journal:  Chemistry       Date:  2020-09-16       Impact factor: 5.236

2.  SmI2-mediated dimerization of indolylbutenones and synthesis of the myxobacterial natural product indiacen B.

Authors:  Nils Marsch; Peter G Jones; Thomas Lindel
Journal:  Beilstein J Org Chem       Date:  2015-09-21       Impact factor: 2.883

  2 in total

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