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11. |
Simple, Efficient Synthesis of 13-nor-2,6(10)-carotadiene, a Potentially Useful Precursor of Carotane- and Tormesane—like Compounds |
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Natural Product Letters,
Volume 5,
Issue 3,
1994,
Page 221-224
JulioG. Urones,
IsidroS. Marcos,
IsabelM. Oliva,
DavidDiez Martín,
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摘要:
(±)—Nerolidol, has been converted into anor—carotane derivative in 46% overall yield.
ISSN:1057-5634
DOI:10.1080/10575639408044063
出版商:Taylor & Francis Group
年代:1994
数据来源: Taylor
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12. |
Synthesis of 1-(β-indolyl)1,3-butadienes, Yuehchukene and Analogues, and Murrapanine via Acid-catalyzed Reactions of β-(1-hydroxybut-3-enyl)indoles |
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Natural Product Letters,
Volume 5,
Issue 3,
1994,
Page 225-232
Yua-Kuang Chen,
Huey-Fen Chung,
Jyh-Horng Sheu,
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摘要:
β-(1-Hydroxybut-3-enyl)indoles, which are prepared in high yields from indole-3-carbonyl compounds, could be converted into 1-(β-indolyl)1,3-butadienes, yuehchukene and derivatives, and murrapanine in one step under various acid-catalyzed reaction conditions in THF. As the reactions of β-(1-hydroxypropenyl)indole1 3with alcohol4and8agave exclusively bisnoryuehchukene7cand trinoryuehchukene7d, respectively, our present work also gives strong evidence to support the asssumption that reactions of this type indeed proceed from a Diels-Alder pathway.
ISSN:1057-5634
DOI:10.1080/10575639408044064
出版商:Taylor & Francis Group
年代:1994
数据来源: Taylor
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13. |
Two new Triterpenoid Saponins, Asterbatanoside F and G, fromAster batangensis |
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Natural Product Letters,
Volume 5,
Issue 3,
1994,
Page 233-240
Yu Shao,
Bing-Nan Zhou,
Long-Ze Lin,
GeoffreyA. Cordell,
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摘要:
Two novel triterpenoid saponins named asterbatanoside F (1) and G (2) were isolated from the roots ofAster batangensisand their structures elucidated as 3-O-β-D-glucopyranosyl-23-O-acetyl-bayogenin-28-O-β-D- glucopyranosyl-(1 → 6) - [α-L-rhamnopyranosyl-(1→2)] β-D-glucopyranoside and 3-O-β-D-glucopyranosyl-bayogenin-28-O-β-D-glucopyranosyl-(1→6)-[α-L-rhamnopyranosyl-(1→2)]-β-D-glucopyranoside by means of spectral data especially 2D NMR including COSY, HETCOR, COLOC, HOHAHA, ROESY and selective INEPT techniques and chemical evidence.
ISSN:1057-5634
DOI:10.1080/10575639408044065
出版商:Taylor & Francis Group
年代:1994
数据来源: Taylor
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14. |
Editorial board page for “Natural Product Letters”, Volume 5, Number 3 |
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Natural Product Letters,
Volume 5,
Issue 3,
1994,
Page -
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PDF (62KB)
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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:10.1080/10575639408044052
出版商:Taylor & Francis Group
年代:1994
数据来源: Taylor
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