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11. |
Alkaloids from some AustralianStephania(Menispermaceae) Species |
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Natural Product Letters,
Volume 3,
Issue 4,
1993,
Page 305-312
JoanneT. Blanchfield,
William Kitching,
DonaldP. A. Sands,
Y.H. Thong,
ColinH. L. Kennard,
KarlA. Byriel,
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摘要:
The alkaloids from forest vines endemic to eastern Australia, vizStephania bancroftiiF. M. Bailey andS. aculeataF. M. Bailey (Menispermaceae) have been examined. The major alkaloids in the tuber of the former species are (-)-tetrahydropalmatine and (-)-stephanine, whereas these are minor components in the leaves, from which we have characterised a C-7 hydroxylated aporphine. The major tuber alkaloids inS. aculeataare (+)-laudanidine and the morphinoid, (-)-amurine whose X-ray structure is presented.
ISSN:1057-5634
DOI:10.1080/10575639308043881
出版商:Taylor & Francis Group
年代:1993
数据来源: Taylor
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12. |
A Hetero Diels-alder Approach to the Synthesis of Castanospermine Analogs: Preparation of 1-O-ethyl-1,6,8a-triepicastanospermine |
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Natural Product Letters,
Volume 3,
Issue 4,
1993,
Page 313-318
Panagiotis Kefalas,
Henri-Philippe Husson,
DavidS. Grierson,
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摘要:
Hetero Diels-Alder reaction of diene7, obtained in four steps from aldehyde4, with Troc-NO8produced the dihydro-2H-1,2-oxazine9in 48% yield. Conversion of this intermediate to the N-deprotected tosylate10followed by ring closure gave the bicyclic product11which was converted to the indolizidine derivative13by N‒O bond cleavage (H2, RaNi) and recyclization under Mitsunobu conditions. Final deprotection of13with mild acid gave the target triepicastanospermine analog3.
ISSN:1057-5634
DOI:10.1080/10575639308043882
出版商:Taylor & Francis Group
年代:1993
数据来源: Taylor
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13. |
Editorial board page for “Natural Product Letters”, Volume 3, Number 4 |
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Natural Product Letters,
Volume 3,
Issue 4,
1993,
Page -
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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:10.1080/10575639308043870
出版商:Taylor & Francis Group
年代:1993
数据来源: Taylor
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