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13,14-Seco-steroids: A New Type of Modified Steroids Containing a Nine-Membered Ring

Само за регистроване кориснике
1999
Аутори
Bjelaković, Mira
Lorenc, Ljubinka
Pavlović, Vladimir D.
Mihailović, Milhailo Lj.
Tinant, Bernard
Declercq, Jean-Paul
Kalvoda, Jaroslav
Чланак у часопису (Објављена верзија)
Метаподаци
Приказ свих података о документу
Апстракт
Oxidations of 14α‐hydroxy‐5α‐cholestan‐3β‐yl acetate (5) with lead tetraacetate under thermal or photolytic conditions or in the presence of iodine proceed mainly by fragmentation of the C(13)−C(14) bond to give as the primary products the 13,18‐didehydro‐13,14‐seco derivative 6 and the (E )‐Δ12‐13,14‐seco ketone 11, respectively. Further transformations of these compounds under conditions of their formation afforded, in addition, the acetoxy derivatives 7 – 9 (from 6), and the D‐homo‐C‐nor compound 12 and (12R,13R)‐epoxide 13 (from 11). Unexpectedly, the photolytic lead‐tetraacetate oxidation of 5 resulted partly (to ca. 20%) in a reversible fragmentation involving scission and recombination of the C(8)−C(14) bond followed by formation of the 14β,22‐ether 10. Possible mechanisms for the observed transformations are discussed.
Кључне речи:
Steroids / Oxidation / Lead-tetraacetate / photolytic conditions / thermal conditions
Извор:
Helvetica Chimica Acta, 1999, 82, 5, 707-721
Издавач:
  • Wiley

DOI: 10.1002/(SICI)1522-2675(19990505)82:5<707::AID-HLCA707>3.0.CO;2-O

ISSN: 0018-019X; 1522-2675

Scopus: 2-s2.0-0032920731
[ Google Scholar ]
15
URI
https://cer.ihtm.bg.ac.rs/handle/123456789/4184
Колекције
  • Radovi istraživača / Researchers' publications
Институција/група
IHTM
TY  - JOUR
AU  - Bjelaković, Mira
AU  - Lorenc, Ljubinka
AU  - Pavlović, Vladimir D.
AU  - Mihailović, Milhailo Lj.
AU  - Tinant, Bernard
AU  - Declercq, Jean-Paul
AU  - Kalvoda, Jaroslav
PY  - 1999
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4184
AB  - Oxidations of 14α‐hydroxy‐5α‐cholestan‐3β‐yl acetate (5) with lead tetraacetate under thermal or photolytic conditions or in the presence of iodine proceed mainly by fragmentation of the C(13)−C(14) bond to give as the primary products the 13,18‐didehydro‐13,14‐seco derivative 6 and the (E )‐Δ12‐13,14‐seco ketone 11, respectively. Further transformations of these compounds under conditions of their formation afforded, in addition, the acetoxy derivatives 7 – 9 (from 6), and the D‐homo‐C‐nor compound 12 and (12R,13R)‐epoxide 13 (from 11). Unexpectedly, the photolytic lead‐tetraacetate oxidation of 5 resulted partly (to ca. 20%) in a reversible fragmentation involving scission and recombination of the C(8)−C(14) bond followed by formation of the 14β,22‐ether 10. Possible mechanisms for the observed transformations are discussed.
PB  - Wiley
T2  - Helvetica Chimica Acta
T1  - 13,14-Seco-steroids: A New Type of Modified Steroids Containing a Nine-Membered Ring
VL  - 82
IS  - 5
SP  - 707
EP  - 721
DO  - 10.1002/(SICI)1522-2675(19990505)82:5<707::AID-HLCA707>3.0.CO;2-O
ER  - 
@article{
author = "Bjelaković, Mira and Lorenc, Ljubinka and Pavlović, Vladimir D. and Mihailović, Milhailo Lj. and Tinant, Bernard and Declercq, Jean-Paul and Kalvoda, Jaroslav",
year = "1999",
abstract = "Oxidations of 14α‐hydroxy‐5α‐cholestan‐3β‐yl acetate (5) with lead tetraacetate under thermal or photolytic conditions or in the presence of iodine proceed mainly by fragmentation of the C(13)−C(14) bond to give as the primary products the 13,18‐didehydro‐13,14‐seco derivative 6 and the (E )‐Δ12‐13,14‐seco ketone 11, respectively. Further transformations of these compounds under conditions of their formation afforded, in addition, the acetoxy derivatives 7 – 9 (from 6), and the D‐homo‐C‐nor compound 12 and (12R,13R)‐epoxide 13 (from 11). Unexpectedly, the photolytic lead‐tetraacetate oxidation of 5 resulted partly (to ca. 20%) in a reversible fragmentation involving scission and recombination of the C(8)−C(14) bond followed by formation of the 14β,22‐ether 10. Possible mechanisms for the observed transformations are discussed.",
publisher = "Wiley",
journal = "Helvetica Chimica Acta",
title = "13,14-Seco-steroids: A New Type of Modified Steroids Containing a Nine-Membered Ring",
volume = "82",
number = "5",
pages = "707-721",
doi = "10.1002/(SICI)1522-2675(19990505)82:5<707::AID-HLCA707>3.0.CO;2-O"
}
Bjelaković, M., Lorenc, L., Pavlović, Vladimir D., Mihailović, M. Lj., Tinant, B., Declercq, J.,& Kalvoda, J.. (1999). 13,14-Seco-steroids: A New Type of Modified Steroids Containing a Nine-Membered Ring. in Helvetica Chimica Acta
Wiley., 82(5), 707-721.
https://doi.org/10.1002/(SICI)1522-2675(19990505)82:5<707::AID-HLCA707>3.0.CO;2-O
Bjelaković M, Lorenc L, Pavlović V, Mihailović ML, Tinant B, Declercq J, Kalvoda J. 13,14-Seco-steroids: A New Type of Modified Steroids Containing a Nine-Membered Ring. in Helvetica Chimica Acta. 1999;82(5):707-721.
doi:10.1002/(SICI)1522-2675(19990505)82:5<707::AID-HLCA707>3.0.CO;2-O .
Bjelaković, Mira, Lorenc, Ljubinka, Pavlović, Vladimir D., Mihailović, Milhailo Lj., Tinant, Bernard, Declercq, Jean-Paul, Kalvoda, Jaroslav, "13,14-Seco-steroids: A New Type of Modified Steroids Containing a Nine-Membered Ring" in Helvetica Chimica Acta, 82, no. 5 (1999):707-721,
https://doi.org/10.1002/(SICI)1522-2675(19990505)82:5<707::AID-HLCA707>3.0.CO;2-O . .

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