A new approach to the synthesis of 3β,23-diacetoxy-24-nor-5-cholene from 3β,21-diacetoxy-5-pregnen-20-one
Synthesis of 3β,23-diacetoxy-24-nor-5-cholene in six steps from 3β,21-diacetoxy-5-pregnen-20-one has been achieved by a new approach. The method would allow to label the side chain of a bile acid at carbon-atom 21. © 1980, All rights reserved.
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| Formato: | JOUR |
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| Acceso en línea: | http://hdl.handle.net/20.500.12110/paper_0039128x_v36_n5_p575_Seldes |
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todo:paper_0039128x_v36_n5_p575_Seldes2023-10-03T14:49:34Z A new approach to the synthesis of 3β,23-diacetoxy-24-nor-5-cholene from 3β,21-diacetoxy-5-pregnen-20-one Seldes, A.M. Anding, C.R. Gros, E.G. 24 norcholest 5 ene 3beta,23 diol diacetate 3beta,21 diacetoxypregn 5 en 20 one bile acid unclassified drug article drug synthesis Synthesis of 3β,23-diacetoxy-24-nor-5-cholene in six steps from 3β,21-diacetoxy-5-pregnen-20-one has been achieved by a new approach. The method would allow to label the side chain of a bile acid at carbon-atom 21. © 1980, All rights reserved. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_0039128x_v36_n5_p575_Seldes |
| institution |
Universidad de Buenos Aires |
| institution_str |
I-28 |
| repository_str |
R-134 |
| collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
| topic |
24 norcholest 5 ene 3beta,23 diol diacetate 3beta,21 diacetoxypregn 5 en 20 one bile acid unclassified drug article drug synthesis |
| spellingShingle |
24 norcholest 5 ene 3beta,23 diol diacetate 3beta,21 diacetoxypregn 5 en 20 one bile acid unclassified drug article drug synthesis Seldes, A.M. Anding, C.R. Gros, E.G. A new approach to the synthesis of 3β,23-diacetoxy-24-nor-5-cholene from 3β,21-diacetoxy-5-pregnen-20-one |
| topic_facet |
24 norcholest 5 ene 3beta,23 diol diacetate 3beta,21 diacetoxypregn 5 en 20 one bile acid unclassified drug article drug synthesis |
| description |
Synthesis of 3β,23-diacetoxy-24-nor-5-cholene in six steps from 3β,21-diacetoxy-5-pregnen-20-one has been achieved by a new approach. The method would allow to label the side chain of a bile acid at carbon-atom 21. © 1980, All rights reserved. |
| format |
JOUR |
| author |
Seldes, A.M. Anding, C.R. Gros, E.G. |
| author_facet |
Seldes, A.M. Anding, C.R. Gros, E.G. |
| author_sort |
Seldes, A.M. |
| title |
A new approach to the synthesis of 3β,23-diacetoxy-24-nor-5-cholene from 3β,21-diacetoxy-5-pregnen-20-one |
| title_short |
A new approach to the synthesis of 3β,23-diacetoxy-24-nor-5-cholene from 3β,21-diacetoxy-5-pregnen-20-one |
| title_full |
A new approach to the synthesis of 3β,23-diacetoxy-24-nor-5-cholene from 3β,21-diacetoxy-5-pregnen-20-one |
| title_fullStr |
A new approach to the synthesis of 3β,23-diacetoxy-24-nor-5-cholene from 3β,21-diacetoxy-5-pregnen-20-one |
| title_full_unstemmed |
A new approach to the synthesis of 3β,23-diacetoxy-24-nor-5-cholene from 3β,21-diacetoxy-5-pregnen-20-one |
| title_sort |
new approach to the synthesis of 3β,23-diacetoxy-24-nor-5-cholene from 3β,21-diacetoxy-5-pregnen-20-one |
| url |
http://hdl.handle.net/20.500.12110/paper_0039128x_v36_n5_p575_Seldes |
| work_keys_str_mv |
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| _version_ |
1782027950913224704 |