dc.contributor |
Aalto-yliopisto |
fi |
dc.contributor |
Aalto University |
en |
dc.contributor.author |
Lajunen, M. |
|
dc.contributor.author |
Koskinen, A. |
|
dc.date.accessioned |
2016-09-23T08:16:42Z |
|
dc.date.issued |
2000 |
|
dc.identifier.citation |
Lajunen , M & Koskinen , A 2000 , ' Hajos-Parrish ketone: approaches toward C-ring prcursors of 7-deoxytaxol ' , Journal of the Chemical Society, Perkin Transactions 1 , no. 1 , pp. 1439-1443 . https://doi.org/10.1039/a909471g |
en |
dc.identifier.other |
PURE UUID: 8896995d-4bef-429a-83d7-6388a25cc00d |
|
dc.identifier.other |
PURE ITEMURL: https://research.aalto.fi/en/publications/8896995d-4bef-429a-83d7-6388a25cc00d |
|
dc.identifier.other |
PURE FILEURL: https://research.aalto.fi/files/7159156/ms076.PDF |
|
dc.identifier.uri |
https://aaltodoc.aalto.fi/handle/123456789/22321 |
|
dc.description.abstract |
Two routes were evaluated for the preparation of multiply functionalized cyclohexane derivatives in a stereocontrolled fashion from readily available Hajos–Parrish ketone 1. Reduction (catalytic or dissolving metal) led to the cis-isomer 8, in stark contrast to previous literature. Finally, modification of earlier steroid chemistry allowed the synthesis of the trans-isomer 14. The latter is a useful intermediate for the synthesis of 7-deoxytaxol derivatives. |
en |
dc.format.extent |
1439-1443 |
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dc.format.mimetype |
application/pdf |
|
dc.language.iso |
en |
en |
dc.relation.ispartofseries |
Journal Chem. Soc., Perkin Trans. |
en |
dc.relation.ispartofseries |
issue 1 |
en |
dc.rights |
openAccess |
en |
dc.title |
Hajos-Parrish ketone: approaches toward C-ring prcursors of 7-deoxytaxol |
en |
dc.type |
A1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä |
fi |
dc.description.version |
Peer reviewed |
en |
dc.contributor.department |
Department of Chemistry |
en |
dc.subject.keyword |
synthesis |
|
dc.subject.keyword |
taxol |
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dc.identifier.urn |
URN:NBN:fi:aalto-201609234325 |
|
dc.identifier.doi |
10.1039/a909471g |
|
dc.type.version |
acceptedVersion |
|