Synthesis of 3/gb-acetoxy-24-norchola-5,20(22)-dien-23-al. a new intermediate for an improved synthesis of [24-14c]-cholesterol
[24-14C]-Cholesterol was synthesized by reaction between the phosphorane derivative of [1-14C]-isobutyltriphenylphosphonium bromide and 3β-acetoxy-24-norchola-5,20(22)-dien-23-al (IX) followed by hydrogenation of the condensation product. The intermediate IX was prepared by two different procedures...
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1973
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Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00224731_v4_n2_p171_Colonna http://hdl.handle.net/20.500.12110/paper_00224731_v4_n2_p171_Colonna |
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paper:paper_00224731_v4_n2_p171_Colonna2023-06-08T14:51:04Z Synthesis of 3/gb-acetoxy-24-norchola-5,20(22)-dien-23-al. a new intermediate for an improved synthesis of [24-14c]-cholesterol aldehyde carbon cholane derivative cholesterol norsteroid pregnenolone article chemistry hydrogenation isotope labeling synthesis Aldehydes Carbon Isotopes Chemistry Cholanes Cholesterol Hydrogenation Isotope Labeling Norsteroids Pregnenolone [24-14C]-Cholesterol was synthesized by reaction between the phosphorane derivative of [1-14C]-isobutyltriphenylphosphonium bromide and 3β-acetoxy-24-norchola-5,20(22)-dien-23-al (IX) followed by hydrogenation of the condensation product. The intermediate IX was prepared by two different procedures both starting from pregnenolone acetate. © 1973. 1973 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00224731_v4_n2_p171_Colonna http://hdl.handle.net/20.500.12110/paper_00224731_v4_n2_p171_Colonna |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
topic |
aldehyde carbon cholane derivative cholesterol norsteroid pregnenolone article chemistry hydrogenation isotope labeling synthesis Aldehydes Carbon Isotopes Chemistry Cholanes Cholesterol Hydrogenation Isotope Labeling Norsteroids Pregnenolone |
spellingShingle |
aldehyde carbon cholane derivative cholesterol norsteroid pregnenolone article chemistry hydrogenation isotope labeling synthesis Aldehydes Carbon Isotopes Chemistry Cholanes Cholesterol Hydrogenation Isotope Labeling Norsteroids Pregnenolone Synthesis of 3/gb-acetoxy-24-norchola-5,20(22)-dien-23-al. a new intermediate for an improved synthesis of [24-14c]-cholesterol |
topic_facet |
aldehyde carbon cholane derivative cholesterol norsteroid pregnenolone article chemistry hydrogenation isotope labeling synthesis Aldehydes Carbon Isotopes Chemistry Cholanes Cholesterol Hydrogenation Isotope Labeling Norsteroids Pregnenolone |
description |
[24-14C]-Cholesterol was synthesized by reaction between the phosphorane derivative of [1-14C]-isobutyltriphenylphosphonium bromide and 3β-acetoxy-24-norchola-5,20(22)-dien-23-al (IX) followed by hydrogenation of the condensation product. The intermediate IX was prepared by two different procedures both starting from pregnenolone acetate. © 1973. |
title |
Synthesis of 3/gb-acetoxy-24-norchola-5,20(22)-dien-23-al. a new intermediate for an improved synthesis of [24-14c]-cholesterol |
title_short |
Synthesis of 3/gb-acetoxy-24-norchola-5,20(22)-dien-23-al. a new intermediate for an improved synthesis of [24-14c]-cholesterol |
title_full |
Synthesis of 3/gb-acetoxy-24-norchola-5,20(22)-dien-23-al. a new intermediate for an improved synthesis of [24-14c]-cholesterol |
title_fullStr |
Synthesis of 3/gb-acetoxy-24-norchola-5,20(22)-dien-23-al. a new intermediate for an improved synthesis of [24-14c]-cholesterol |
title_full_unstemmed |
Synthesis of 3/gb-acetoxy-24-norchola-5,20(22)-dien-23-al. a new intermediate for an improved synthesis of [24-14c]-cholesterol |
title_sort |
synthesis of 3/gb-acetoxy-24-norchola-5,20(22)-dien-23-al. a new intermediate for an improved synthesis of [24-14c]-cholesterol |
publishDate |
1973 |
url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00224731_v4_n2_p171_Colonna http://hdl.handle.net/20.500.12110/paper_00224731_v4_n2_p171_Colonna |
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1768544538482180096 |