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1. |
A New Flavonol Glycoside from Eucalyptus globulous Subsp. Maidenii |
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Natural Product Letters,
Volume 7,
Issue 3,
1995,
Page 163-167
LawrenceO. A. Manguro,
KavakaW. Mukonyi,
JosephK. Githiomi,
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摘要:
A new flavonol glycoside characterized as quercetin 8-C-α-β-rhamnosyl (1→2) glucoside (1) together with quercetin 3-O-β-D-glucoside (2), quercetin 3-O-α-L-rhamnoside (3), quercetin (4) and kaempferol (5), have been isolated from the methanol extract of the leaves.
ISSN:1057-5634
DOI:10.1080/10575639508043206
出版商:Taylor & Francis Group
年代:1995
数据来源: Taylor
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2. |
A Blue Pigment Derived from Rosmarinic Acid and FeSO4is Responsible for the Blue Pigment Secreted into the Medium byLavandula x intermediaCell Cultures Grown in the Dark |
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Natural Product Letters,
Volume 7,
Issue 3,
1995,
Page 169-175
T. López-Arnaldos,
M. López-Serrano,
A.Ros Barceló,
A.A. Calderón,
J.M. Zapata,
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摘要:
Rosmarinic acid (α-O-caffeoyl-3,4-dihydroxy phenyllactic acid) is the main phenolic constituent (1.0–7.0 μmol/kg) present in methanolic extracts of the medium fromLavandula × intermediacell cultures which have been grown on agar gel containing Murashige & Skoog medium. In this medium, the concentration of FeSO4is 100 μmol/kg. Since rosmarinic acid yields a blue pigment upon reaction with FeSO4(λmax= 572 nm and ϵ572= 3,820 M−1cm−1at pH 6.0), this this pigment appears to be the main compound responsible for the blue colour which is secreted into the medium byLavandula × intermediacell cultures grown in the dark.
ISSN:1057-5634
DOI:10.1080/10575639508043207
出版商:Taylor & Francis Group
年代:1995
数据来源: Taylor
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3. |
The Biosynthetic Origin of the Central One-Carbon Unit of Phenylphenalenones inAnigozanthos preissii |
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Natural Product Letters,
Volume 7,
Issue 3,
1995,
Page 177-182
Dirk Hölscher,
Bernd Schneider,
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摘要:
The biosynthetic origin of all 19 carbon atoms of the phenyl-phenalenones was established by13C NMR analysis of hydroxyanigorufone, isolated from cultured roots ofAnigozanthos preissiiafter administration of13C labelled precursors. High incorporation of C-2 of [2-13C]acetate into the central carbon atom for the first time unambiguously proved the origin of this C1unit of phenylphenalenones.
ISSN:1057-5634
DOI:10.1080/10575639508043208
出版商:Taylor & Francis Group
年代:1995
数据来源: Taylor
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4. |
Sandensolide: A New Dihydroxycembranolide from the Soft Coral,Sinularia sandensisVerseveldt of the Indian Ocean |
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Natural Product Letters,
Volume 7,
Issue 3,
1995,
Page 183-190
A.S. R. Anjaneyulu,
G.Venkateswara Rao,
K.S. Sagar,
K.Ravi Kumar,
K.Chandra Mohan,
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摘要:
A new dihydroxycembranolide, sandensolide has been isolated along with (+)-sinulariolide from the ethyl acetate extract of the soft coralSinularia sandensisVerseveldt. The structure and stereochemistry of the new compound was determined by its spectral data [UV, IR,1H &13C NMR, 2D NMR (1H-1H COSY) and Mass], chemical conversion and X-ray analysis.
ISSN:1057-5634
DOI:10.1080/10575639508043209
出版商:Taylor & Francis Group
年代:1995
数据来源: Taylor
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5. |
Voafinine andN1-Methylvoafinine, Novel Aspidosperma Alkaloids fromTabernaemontana |
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Natural Product Letters,
Volume 7,
Issue 3,
1995,
Page 191-195
Toh-Seok Kam,
S. Anuradha,
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摘要:
Novel indole alkaloids of the aspidosperma-type were obtained in minor amounts from the leaf extract ofTabernaemontana divaricata(double flower variety). The structures of these alkaloids were elucidated by spectral methods.
ISSN:1057-5634
DOI:10.1080/10575639508043210
出版商:Taylor & Francis Group
年代:1995
数据来源: Taylor
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6. |
Synthesis of Vinca Alkaloids and Related Compounds, 76.1Synthesis and Ring Transformations of Compounds with the Aspidospermane- and D-Noraspidospermane Skeleton. A Formal Synthesis Of (±)-12-Demethoxy-N(1)-Acetyl-Cylindrocarine |
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Natural Product Letters,
Volume 7,
Issue 3,
1995,
Page 197-204
György Kalaus,
István Vágó,
István Greiner,
MáriaKajtár Peredy,
János Brlik,
Lajos Szabó,
Csaba Szántay,
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摘要:
Reaction of compound (4) with (5) give a mixture of the isomers (7) and (8) through the intermediate (1). Further conversions led through the oxo- (9), (10) and thioxo (11), (12) derivatives to (±)-19-ethoxycarbonyl-19-demethylvincadifformine (3), and (±)-18-methoxycarbonyl-D(14)-norvincadifformine (13). The preparation of the former compound constitutes the formal synthesis of (±)-12-demethoxy-N(1)-acetylcylindrocarine (2). Oxidative ring transformation of the latter gave (±)-21-methoxycarbony 1-D(18)-norapovincamine (14).
ISSN:1057-5634
DOI:10.1080/10575639508043211
出版商:Taylor & Francis Group
年代:1995
数据来源: Taylor
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7. |
Absolute Configuration of (-)-Magnofargesin fromMagnolia fargesii |
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Natural Product Letters,
Volume 7,
Issue 3,
1995,
Page 205-207
Mitsuo Miyazawa,
Hiroyuki Kasahara,
Hiromu Kameoka,
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摘要:
The absolute configuration assignment of (-)-magnofargesin (1) was achieved by the isomerization of1to (+)-magnolin.
ISSN:1057-5634
DOI:10.1080/10575639508043212
出版商:Taylor & Francis Group
年代:1995
数据来源: Taylor
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8. |
New Phenolic and Quinone-methide Triterpenes fromMaytenusSpecies (Celastraceae) |
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Natural Product Letters,
Volume 7,
Issue 3,
1995,
Page 209-218
AntonioG. Gonzalez,
NelsonL. Alvarenga,
Felix Rodriguez,
AngelG. Ravelo,
IgnacioA. Jimenez,
IsabelL. Bazzocchi,
MahabirP. Gupta,
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摘要:
The new phenolic triterpenes, blepharodol (5) and 7α-hydroxy-blepharodol (6) were isolated fromMaytenus blepharodesand canarol (8), 7α-hydroxy-canarol (9), 7-hydroxy-6-oxoiguesterol (11), canaradial (12) and the triterpene methylene quinones iguesteroquinone (13) and 7α-hydroxy-7,8-dihydro-iguesterin (14) and were isolated fromMaytenus canariensis. Their structures were elucidated by means of1H and13C NMR spectroscopic studies, including homo and heteronuclear correlations, DEPT, COSY, HMQC and HMBC experiments. These products are intermediates in the biogenetic pathway of methylene quinone triterpenes.
ISSN:1057-5634
DOI:10.1080/10575639508043213
出版商:Taylor & Francis Group
年代:1995
数据来源: Taylor
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9. |
New Alkaloids fromSarcomelicope dogniensis1 |
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Natural Product Letters,
Volume 7,
Issue 3,
1995,
Page 219-225
Sofia Mitaku,
Alexios-Leandros Skaltsounis,
Francois Tillequin,
Michel Koch,
Jacques Pusset,
Thierry Sevenet,
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摘要:
Two novel alkaloids, 1-oxo-1,2-dihydro-12-demethyl-12-hydroxyacronycine (1) and 2,3-dicarbomethoxy-1-methyl-4(1H)-quinolinone (3) have been isolated from the leaves ofSarcomelicope dogniensis. The biogenesis of this latter most probably involves oxidation of the A aromatic ring of a 1,2,3,4-tetra-O-subtituted acridone, such as melicopidine.
ISSN:1057-5634
DOI:10.1080/10575639508043214
出版商:Taylor & Francis Group
年代:1995
数据来源: Taylor
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10. |
Semisynthesis of (+) (16S, 20S, 21R) 16-Hydroxymethyl-Goniomitine from (-) Vincadifformine |
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Natural Product Letters,
Volume 7,
Issue 3,
1995,
Page 227-234
G. Lewin,
C. Schaeffer,
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摘要:
Starting from (-) vincadifformine (1), (+) 16-hydroxymethylgoniomitine (10), a derivative of the indole alkaloid (-)goniomitine (5), was synthesizedviathe rearranged compound3.
ISSN:1057-5634
DOI:10.1080/10575639508043215
出版商:Taylor & Francis Group
年代:1995
数据来源: Taylor
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