|
11. |
Two New Naturally Occurring Pyrrole Derivatives from the Tropical Marine SpongeAgelas oroides |
|
Natural Product Letters,
Volume 5,
Issue 2,
1994,
Page 141-146
GabrieleM. König,
AnthonyD. Wright,
Preview
|
PDF (226KB)
|
|
摘要:
Continued investigation into the natural products chemistry of the tropical marine spongeAgelas oroides, collected from the Great Barrier Reef, Queensland, Australia, has yielded two new naturally occurring pyrrole derivatives,1and2. The structures of1and2were determined from the interpretation of their 1D and 2D NMR, UV, IR and mass spectral data.
ISSN:1057-5634
DOI:10.1080/10575639408044048
出版商:Taylor & Francis Group
年代:1994
数据来源: Taylor
|
12. |
A New Norditerpenoid Alkaloid From Seeds of Aconitum Napellus SSP. vulgare1 |
|
Natural Product Letters,
Volume 5,
Issue 2,
1994,
Page 147-151
Hongmei Liu,
Alfred Katz,
Preview
|
PDF (195KB)
|
|
摘要:
A new norditerpenoid alkaloid, 16ß-acetoxycardiopetaline (2), and two known alkaloids, neoline (1) and senbusine A (3), were isolated for the first time from the seeds of Aconitum napellus ssp. vulgare. The structure of alkaloid 2 was established on the basis of ir, mass,1H-nmr,13C-nmr, DEPT and 2D-nmr spectrometry.
ISSN:1057-5634
DOI:10.1080/10575639408044049
出版商:Taylor & Francis Group
年代:1994
数据来源: Taylor
|
13. |
Diastereoselective Three-center Michael Addition. Part 2.1A New Entry into the Prelog-Djerassi Lactone Framework |
|
Natural Product Letters,
Volume 5,
Issue 2,
1994,
Page 153-155
Nicole Ouvrard,
Jean Rodriguez,
Maurice Santelli,
Preview
|
PDF (163KB)
|
|
摘要:
The chiral intermediates (+)-11and (+)-12, are synthetized by using the diastereoselective three-center Michael addition of the chiral β-ketoester4to crotonaldehyde5allowing a new efficient entry into the synthesis of the Prelog-Djerassi lactone and related compounds.
ISSN:1057-5634
DOI:10.1080/10575639408044050
出版商:Taylor & Francis Group
年代:1994
数据来源: Taylor
|
14. |
Synthesis of Both Enantiomers of Methyl 3-methyloctanoate, Key Component for the Scent of African Orchids and Determination of their Absolute Configuration |
|
Natural Product Letters,
Volume 5,
Issue 2,
1994,
Page 157-164
Takeshi Kitahara,
KangSeung Hyun,
Shigeyuki Tamogami,
Roman Kaiser,
Preview
|
PDF (384KB)
|
|
摘要:
Synthesis of enantiomers of methyl 3-methyloctanoate2was achieved starting from enantiomers of methyl 3-hydroxy-2-methylpropanoate3in 9 steps. (S)-Enantiomer was shown to be identical with the naturally occurring isomer by GC analysis using a capillary column with chiral stationary phase. Interestingly, unnatural (R)-enantiomer has stronger floral note than natural (S)-enantiomer.
ISSN:1057-5634
DOI:10.1080/10575639408044051
出版商:Taylor & Francis Group
年代:1994
数据来源: Taylor
|
15. |
Editorial board page for “Natural Product Letters”, Volume 5, Number 2 |
|
Natural Product Letters,
Volume 5,
Issue 2,
1994,
Page -
Preview
|
PDF (64KB)
|
|
摘要:
This is a scanned image of the original Editorial Board page(s) for this issue.
ISSN:1057-5634
DOI:10.1080/10575639408044037
出版商:Taylor & Francis Group
年代:1994
数据来源: Taylor
|
|