|
1. |
Indicusin-A Pregnane Diester Triglycoside from Hemidesmus indicus R. Br |
|
Natural Product Letters,
Volume 6,
Issue 2,
1995,
Page 81-86
Desh Deepak,
Sanjay Srivastav,
Anakshi Khare,
Preview
|
PDF (222KB)
|
|
摘要:
A novel pregnane oligoglycoside viz. Indicusin (1) was isolated from CHCl3-EtOH (3:2) fraction ofHemidesmus indicusR Br. (family Asclepiadaceae). With the help of FABMS,1H NMR,13C NMR spectroscopy and chemical transformations, the structure of1was defined as 11α, 12β-di-O-acetyl-orgogenin-3-O-β-D-cymaropyranosyl (1→4)-O-β-D-cymaropyranosyl (1→4)-O-β-D-cymaropyranoside.
ISSN:1057-5634
DOI:10.1080/10575639508044094
出版商:Taylor & Francis Group
年代:1995
数据来源: Taylor
|
2. |
Asteryunnanosides C and D, two Novel Triterpenoid Saponins fromAster yunnanensisFranch |
|
Natural Product Letters,
Volume 6,
Issue 2,
1995,
Page 87-93
Yu Shao,
Bing-Nan Zhou,
Preview
|
PDF (324KB)
|
|
摘要:
Two novel triterpene glycosides, asteryunnanosides C (1) and D (2) were isolated fromAster yunnanensisFranch. On the basis of chemical degradation and spectroscopic data, including 2D NMR techniques, their structures were elucidated as 28-O-α-L-rhamnopyranosyl-(1→2)-β-D-glucopyranoside and 28-O-β-D-glucopyranosyl-(1→2)-β-D-glucopyranoside of 2α, 3β-dihydroxy-olean- 12-en-28-oic acid respectively.
ISSN:1057-5634
DOI:10.1080/10575639508044095
出版商:Taylor & Francis Group
年代:1995
数据来源: Taylor
|
3. |
Ranuncoside VII - A New Oleanane Glycoside FromHydrocotyle ranunculoides |
|
Natural Product Letters,
Volume 6,
Issue 2,
1995,
Page 95-102
MariaM. Corsaro,
MarinaDella Greca,
Antonio Fiorentino,
Pietro Monaco,
Lucio Previtera,
Preview
|
PDF (409KB)
|
|
摘要:
A new oleanane glycoside, named ranuncoside VII, was identified as 3-O-[α-L-arabinopyranosyl-(1→6)-β-D-glucopyranosyl]-13β,28-epoxyolean-11-ene-3β, 15α,16α,21β,22α-pentol by chemical and spectroscopic studies. The aglycone structure was confirmed by hemisynthesis from R1-barrigenol.
ISSN:1057-5634
DOI:10.1080/10575639508044096
出版商:Taylor & Francis Group
年代:1995
数据来源: Taylor
|
4. |
The Reaction of Perezone and Isoperezone with Hydroxylamine: A Surprisingly Facile Method for Introducing an NH2Group into the Quinone Functionality |
|
Natural Product Letters,
Volume 6,
Issue 2,
1995,
Page 103-109
RaúlG. Enríquez,
Benjamín Ortiz,
Enrique Alducin,
Fernando Walls,
Dino Gnecco,
Margaret Yu,
WilliamF. Reynolds,
Preview
|
PDF (319KB)
|
|
摘要:
An unusual mode of reaction of hydroxylamine hydrochloride catalyzed by zinc acetate, involving nucleophilic attack upon the perezone1lband isoperezone quinone systems, with further dehydration to produce the corresponding amino derivatives2and5is described.
ISSN:1057-5634
DOI:10.1080/10575639508044097
出版商:Taylor & Francis Group
年代:1995
数据来源: Taylor
|
5. |
9,10-Dihydrophenanthrene Glucosides fromJuncus effusus |
|
Natural Product Letters,
Volume 6,
Issue 2,
1995,
Page 111-117
MarinaDella Greca,
Antonio Fiorentino,
Antonio Molinaro,
Pietro Monaco,
Lucio Previtera,
Preview
|
PDF (269KB)
|
|
摘要:
Four 9,10-dihydrophenanthrene glucosides have been isolated fromJuncus effususand their structures confirmed on spectroscopic grounds and by semisynthesis. The results of a cytotoxic assay are also reported.
ISSN:1057-5634
DOI:10.1080/10575639508044098
出版商:Taylor & Francis Group
年代:1995
数据来源: Taylor
|
6. |
Alkaloids fromNitraria billardieri |
|
Natural Product Letters,
Volume 6,
Issue 2,
1995,
Page 119-125
MayYing Shen,
JoséAngelo Zuanazzi,
Christiane Kan,
Jean-Charles Quirion,
Henri-Philippe Husson,
I.R. C. Bick,
Preview
|
PDF (278KB)
|
|
摘要:
Five alkaloids have been isolated and identified inNitraria billardierifrom Australia. They consist of schoberine1, nitraramine21-epinitraramine3, nitrarine4and 3-epinitrarine5. Complete assignment of their NMR spectra is presented.
ISSN:1057-5634
DOI:10.1080/10575639508044099
出版商:Taylor & Francis Group
年代:1995
数据来源: Taylor
|
7. |
Stereocontrolled Synthesis of Polyenic Ketones from Marine Opisthobranchs |
|
Natural Product Letters,
Volume 6,
Issue 2,
1995,
Page 127-132
Rosana Alvarez,
Susana Lopez,
AngelR. De Lera,
Preview
|
PDF (335KB)
|
|
摘要:
A new stereocontrolled synthesis of a series of polyenic ketones isolated from marine opisthobranchs, namely lignarenone A, lignarenone B and 3-methylnavenone B, is described, which uses the Suzuki reaction in the key step. Thus, the thallium-accelerated, palladium-catalyzed cross-coupling reactions of (E)-1-alkenylboronic acids and alkenyl iodides constitutes an efficient procedure for the preparation of alkyl-substituted polyenes with uniform configuration.
ISSN:1057-5634
DOI:10.1080/10575639508044100
出版商:Taylor & Francis Group
年代:1995
数据来源: Taylor
|
8. |
Glaucanisin, A New Acetogenin fromAnnona glauca |
|
Natural Product Letters,
Volume 6,
Issue 2,
1995,
Page 133-138
A-I. Waechter,
R. Hocquemiller,
A. Laurens,
A. Cavé,
Preview
|
PDF (255KB)
|
|
摘要:
Glaucanisin(1), a new adjacent bis-tetrahydrofuran acetogenin, was isolated together with a known compound, rolliniastatin-2(2)from the CH2Cl2extract ofAnnona glaucaseeds. NMR and mass spectroscopic methods were used for the structure elucidation of glaucanisin, through comparison with the spectral data of rolliniastatin-2 (= bullatacin).
ISSN:1057-5634
DOI:10.1080/10575639508044101
出版商:Taylor & Francis Group
年代:1995
数据来源: Taylor
|
9. |
Preparation of 7-Triethylsilylbaccatin III Using a Regioselective Reductive Deacetylation |
|
Natural Product Letters,
Volume 6,
Issue 2,
1995,
Page 139-145
Arindam Chatterjee,
Sukanta Bhattacharyya,
JamesD. McChesney,
HalaN. Eisohly,
JohnS. Williamson,
Preview
|
PDF (284KB)
|
|
摘要:
The immediate precursor for the semi-synthesis of taxol, 7-triethylsilylbaccatin III (6), has been prepared from 10-DAB (3) using a Bu4NBH4/ LiCl regioselective deacetylation as the key step.
ISSN:1057-5634
DOI:10.1080/10575639508044102
出版商:Taylor & Francis Group
年代:1995
数据来源: Taylor
|
10. |
A Practical and Inexpensive Synthesis of the TaxolC-13 Side Chain;N-Benzoyl-(2R,3S)-3-Phenylisoserine |
|
Natural Product Letters,
Volume 6,
Issue 2,
1995,
Page 147-152
RanjanP. Srivastava,
JamesD. McChesney,
Preview
|
PDF (268KB)
|
|
摘要:
In an effort towards the development of a facile synthesis ofN-benzoyl-(2R,3S)-3-phenylisoserine (3), an important subunit of taxol known as the “taxolC-13 side chain”, which can easily be handled in large scale production as well as meet industrial safety requirements, we present here an efficient and inexpensive synthesis of the taxol side chain via a classical resolution technique. This synthesis represents the most practical preparation of the taxol side chain developed to date.
ISSN:1057-5634
DOI:10.1080/10575639508044103
出版商:Taylor & Francis Group
年代:1995
数据来源: Taylor
|
|