Zuordnung der 1H-NMR-Spektren von Depsiden, Depsidonen, Depsonen und Dibenzofuranen aus Flechten durch NOE-Differenzspektroskopie / Assignment of 1H NMR Spectra of Depsides, Depsidones, Depsones and Dibenzofurans from Lichens by NOE Difference Spectroscopy

1989 ◽  
Vol 44 (9) ◽  
pp. 1117-1123 ◽  
Author(s):  
Jasmin Jakupovic ◽  
Siegfried Huneck
Keyword(s):  
Methyl Ester ◽  
1H Nmr ◽  
Nmr Spectra ◽  
Usnic Acid ◽  
Acid Methyl Ester ◽  
Difference Spectroscopy ◽  
H Nmr ◽  
Acid Methyl ◽  
Lichen Substances ◽  
Noe Difference Spectroscopy

The 1H NMR spectra of the following lichen substances have been correlated by NOE difference spectroscopy: atranorin, barbatic acid, diffractaic acid, nephroarctin, perlatolic acid, planaic acid methyl ester, pseudocyphellarin A, sphaerophorin (depsides), hypoprotocetraric acid, lobaric acid, pannarin, physodalic acid, psoromic acid, stictic acid (depsidones), picrolichenic acid (depsone), di-O-methyl-pannaric acid dimethylester, pannaric acid, porphyrilic acid, schizopeltic acid, strepsilin, and usnic acid (dibenzofurans).

scholarly journals CHEMICAL CONSTITUENTS OF Bischofia javanica

2017 ◽  
Vol 55 (2) ◽  
pp. 188
Author(s):  
Nguyen Thi Mai
Keyword(s):  
Methyl Ester ◽  
Gallic Acid ◽  
Nmr Spectra ◽  
Methanol Extract ◽  
Chemical Constituents ◽  
Acid Methyl Ester ◽  
First Report ◽  
Acid Methyl ◽  
Bischofia Javanica ◽  
Reported Data

From the methanol extract of Bischofia javanica leaves, five compounds including 5'-b-D-glucopyranosyloxyjasmonic acid methyl ester (1), 2-(4-hydroxy-3-methoxyphenyl)ethyl-O-β-D-glucopyranoside (2), hexyl-O-β-D-glucopyranoside (3), friedelan-3-one (4), and gallic acid (5) were isolated. Their structures were elucidated by NMR spectra as well as in comparison with previous reported data. This is the first report of 1 and 2 from Bischofia javanica.

1H NMR and X-ray conformational analyses of (+)-corydalic acid methyl ester, a 6,7-secoberbine alkaloid

1997 ◽  
pp. 631-636 ◽  
Author(s):  
Miyoko Kamigauchi ◽  
Yuko Noda ◽  
Kinuko Iwasa ◽  
Makiko Sugiura ◽  
Zjujiro Nishijo ◽  
...  
Keyword(s):  
Methyl Ester ◽  
1H Nmr ◽  
Acid Methyl Ester ◽  
X Ray ◽  
Acid Methyl

Pannarsäure und Porphyrilsäuremethylester — Sekundärstoffe der Flechtengattung Psoroma / Pannaric Acid and Prophyrilic Acid Methyl Ester Lichen Substances in the Genus Psorma

1981 ◽  
Vol 36 (9-10) ◽  
pp. 893-895 ◽  
Author(s):  
B. Renner ◽  
A. Henssen ◽  
E. Gerstner
Keyword(s):  
Mass Spectrometry ◽  
New Species ◽  
Methyl Ester ◽  
Acid Methyl Ester ◽  
The Novel ◽  
Acid Methyl ◽  
Vis Spectroscopy ◽  
Lichen Substances ◽  
Unknown Structure ◽  
First Time

Abstract The novel liehen substance porphyrilic acid methyl ester and pannaric acid are reported the first time in the lichen genus Psoroma. They are constituents in the two varieties of the new species Psoroma tenue as well as in members of the Psoroma hypnorum/paleaceum aggr. and in a hitherto underscribed species from the southern hemisphere. Both dibenzofuranes are characterized by mass spectrometry and UV/VIS spectroscopy. A third compound of unknown structure (Ut) has been found additionally in the two varieties of P. tenue and in some specimens of the P. hypnorum/paleaceum group.

Isolation of (23R) 3α, 7α,23-trihydroxy-5β-cholan-24-oic (β-phocaecholic) acid from duck bile. 1H NMR spectra of its derivatives

1986 ◽  
Vol 51 (8) ◽  
pp. 1722-1730 ◽  
Author(s):  
Jiří Klinot ◽  
Milan Jirsa ◽  
Eva Klinotová ◽  
Karel Ubik ◽  
Jiří Protiva
Keyword(s):  
Bile Acid ◽  
Methyl Ester ◽  
1H Nmr ◽  
Marine Mammals ◽  
Nmr Spectra ◽  
Chemical Shifts ◽  
1H Nmr Spectra ◽  
Methyl Groups ◽  
H Nmr ◽  
Derivatives Of

(23R) 3α, 7α,23-Trihydroxy-5β-cholan-24-oic acid (IV) - a bile acid typical of some marine mammals - was now isolated from duck bile. Acid IV was characterized as derivatives V - VIII, XI and XII and oxidatively degraded to derivatives of 24-nor-5β-cholan-23-oic acid, XIII - XVIII. The 1H NMR spectra of these compounds and (23S) methyl ester X are discussed and the effect of substitution in position 23 on the chemical shifts of the methyl groups is summarized.

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