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11. |
A New Furanosesquiterpene fromBursera LeptophloeosMarth |
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Natural Product Letters,
Volume 8,
Issue 4,
1996,
Page 285-289
EvelineS. Barreira,
F.J. Queiroz Monte,
Raimundo Braz-filho,
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摘要:
One new furanosesquiterpene (1) was isolated from root barks ofBursera leptophloeos.The structure of this sesquisterpenoid was elucidated from spectral data.
ISSN:1057-5634
DOI:10.1080/10575639608044909
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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12. |
4-Acetyl Annonacin and 4-Acetyl Xylomaticin: Two Novel Bioactive Mono-Tetrahydrofuran Annonaceous Acetogenins fromAsimina Longifolia(Annonaceae) |
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Natural Product Letters,
Volume 8,
Issue 4,
1996,
Page 291-298
Qing Ye,
Lu Zeng,
Guoen Shi,
Dean Evert,
JerryL. McLaughlin,
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摘要:
Two novel bioactive acetogenins, 4-acetyl annonacin (1) and 4-acetyl xylomaticin (2), were isolated from the leaves and twigs ofAsimina longifoliaK. (Annonaceae) by directing the fractionation with the brine shrimp lethality test. 1 and 2 each has a mono-tetrahydrofuran (THF) ring with two flanking hydroxyl groups and an α, β-unsaturated γ-lactone with a 4-acetoxyl. The presence of acetoxyl groups is a feature rarely found in the Annonaceous acetogenins. 1 and 2 showed potent and selective cytotoxicities among six human tumor cell lines.
ISSN:1057-5634
DOI:10.1080/10575639608044910
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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13. |
Insecticidal Alkaloid AgainstDrosophila Melanogasterfrom Tubers ofCorydalis Bulbosa |
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Natural Product Letters,
Volume 8,
Issue 4,
1996,
Page 299-302
Mitsuo Miyazawa,
Kimio Yoshio,
Yukio Ishikawa,
Hiromu Kameoka,
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摘要:
Insecticidal alkaloid, (−)-canadine was isolated under bioassay guide ofDrosophila melanogasterMeigen. from MeOH extract of tubers of Corydalis bulbosa. Insecticidal activity against larvae; (−)-canadine showed 99.7% of larvae were dead at 1.40 μ mol/ml diet concentration, and the LC50value was 0.9 μmol/ml diet concentration. Acute toxicity against adults; (−)-canadine showed 75% of adults were dead at 5.0 μg /adult, and the LD50value was 2.5μg/adult.
ISSN:1057-5634
DOI:10.1080/10575639608044911
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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14. |
Microbial Oxidation of Citronellol byGlomerella Cingulata |
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Natural Product Letters,
Volume 8,
Issue 4,
1996,
Page 303-305
Mitsuo Miyazawa,
Hirokazu Nankai,
Hiromu Kameoka,
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摘要:
3,7-dimethyl-l,6,7-octanetriol was obtained on the microbial transformation of citronellol using plant pathogenic fungus,Glomerella cingulataas a biocatalyst.
ISSN:1057-5634
DOI:10.1080/10575639608044912
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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15. |
An Insecticidal Alkaloid AgainstDrosophila Melanogasterfrom Rhizomes ofNuphar JaponicumDC |
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Natural Product Letters,
Volume 8,
Issue 4,
1996,
Page 307-310
Mitsuo Miyazawa,
Kimio Yoshio,
Yukio Ishikawa,
Hiromu Kameoka,
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摘要:
(−)-7-epi-Deoxynupharidine was isolated as an insecticidal alkaloid by bioassay-guided fractionation from MeOH extract of rhizomes ofNuphar japonicumDC. Insecticidal activity against larvae ofD. melanogaster, (−)-7-epi-deoxynupharidine showed that 48.3% of larvae were dead at 4.29μmol/ml diet concentration, and the LC50value was 4.33μmol/ml diet concentration. Acute toxicity against adults ofD. melanogaster, (−)-7-epi-deoxynupharidine showed that 80% of adults were dead at 1.0μg/adult, and the LD50value was 0.86μg/adult.
ISSN:1057-5634
DOI:10.1080/10575639608044913
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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16. |
An Unexpected Spirodiketone Obtained During Seco-Isopimarene Cyclization |
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Natural Product Letters,
Volume 8,
Issue 4,
1996,
Page 311-315
AngeloC. Pinto,
Rosǎngela deA. Epifanio,
Walter Frankmölle,
William Fenical,
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摘要:
During an investigation of the base-induced transformation of secoisopimarene 1 to gibberellin analog 2, an unexpected solvent-specific cyclization occurred generating a bicyclo[3.2.1]spirodiketone of an unexpected structure class. The structure of this interesting reaction product has been fully defined using comprehensive 2D NMR methods.
ISSN:1057-5634
DOI:10.1080/10575639608044914
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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17. |
Tandem Acylation - Cycloalkylation with Cyclohexene-1-Acetic Acid: A New Entry to Phenanthrene Alkaloids |
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Natural Product Letters,
Volume 8,
Issue 4,
1996,
Page 317-324
M.M. V. Ramana,
PrashantV. Potnis,
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摘要:
Tandem acylation - cycloalkylation of 3,4 - dimethoxy-phenylethylamine (1) with cyclohexene -1-acetic acid (2) in polyphosphoric acid (PPA) afforded 8 - (2 - aminoethyl) - 1,2,3,4,4a,9,10,10a - octahydro - 9 - oxo - phenanthrene (3) which on dehydrogenation with Pd - C, followed by sequentialN- methylation gaveN- noratherosperminine (5) and atherosperminine (6) in good yields.
ISSN:1057-5634
DOI:10.1080/10575639608044915
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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18. |
Editorial board page for “Natural Product Letters”, Volume 8, Number 4 |
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Natural Product Letters,
Volume 8,
Issue 4,
1996,
Page -
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PDF (78KB)
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摘要:
This is a scanned image of the original Editorial Board page(s) for this issue.
ISSN:1057-5634
DOI:10.1080/10575639608044898
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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