2001
DOI: 10.1016/s0003-2670(01)01204-1
|View full text |Cite
|
Sign up to set email alerts
|

Computer-aided method for identification of components in essential oils by 13 C NMR spectroscopy

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
13
0

Year Published

2002
2002
2020
2020

Publication Types

Select...
10

Relationship

0
10

Authors

Journals

citations
Cited by 21 publications
(13 citation statements)
references
References 39 publications
0
13
0
Order By: Relevance
“…RI (retention indices): 1 calculated on an RTx ® ‐5 MS column according to Van den Dool and Kratz , based on a homologous series of normal alkanes; 2 according to Adams ; 3 according to Ferreira et al . .…”
Section: Resultsmentioning
confidence: 99%
“…RI (retention indices): 1 calculated on an RTx ® ‐5 MS column according to Van den Dool and Kratz , based on a homologous series of normal alkanes; 2 according to Adams ; 3 according to Ferreira et al . .…”
Section: Resultsmentioning
confidence: 99%
“…The essential oil constituents identification was carried out by comparing their recorded mass spectra with those stored in the National Institute of Standards and Technology Mass Spectral database (NIST 17 database) or with authentic compounds and confirmed by comparison of their retention index with authentic compounds reported in the literature [58]. The relative percent of each component in essential oil was counted by the area normalization method.…”
Section: Identification Of the Essential Oil Chemical Constituentsmentioning
confidence: 99%
“…In the present paper, we report an investigation of a hexane extract of fruits of a T. hirta specimen, which allowed us to characterize nine terpenoids, including a novel cycloartane-type triterpene named hirtinone ( 1 ), five protolimonoids: nilocitin ( 2 ) [10,11], dihydronilocitin B [10,11] ( 3 ), melianone epimers ( 4 ) and ( 5 ) [11,12], piscidinol A ( 6 ) [10,11,13] and melianone lactone ( 7 ) [11,12], the tertranortriterpenoid hirtin ( 8 ) [14] and the sequiterpene spathulenol ( 9 ) [15]. The structures were established by spectrometric techniques, mainly HRESIMS and 1D and 2D NMR, and comparative analysis with literature values.…”
Section: Introductionmentioning
confidence: 99%