Ministry of Science and Enviroment of Serbia (Part of the project “Synthesis and chemical transformations of steroidal and modified steroid molecules” – Project No. 1702)

Link to this page

http://cer.ihtm.bg.ac.rs/APP/faces/project.xhtml?project_id=Ministry+of+Science+and+Enviroment+of+Serbia+%28Part+of+the+project+%E2%80%9CSynthesis+and+chemical+transformations+of+steroidal+and+modified+steroid+molecules%E2%80%9D+%E2%80%93+Project+No.+1702%29&item_offset=0&author_offset=0&sort_by=dc.date.issued

Ministry of Science and Enviroment of Serbia (Part of the project “Synthesis and chemical transformations of steroidal and modified steroid molecules” – Project No. 1702)

Authors

Publications

Synthesis of 5-azaandrostane-3β,17β-diol protected at the 17β-hydroxyl group

Pavlović, Vladimir D.; Dabović, Milan; Martinović, Saša B.; Lorenc, Ljubinka; Kalvoda, J

(Serbian Chemical Society, 2004) 

TY  - JOUR
AU  - Pavlović, Vladimir D.
AU  - Dabović, Milan
AU  - Martinović, Saša B.
AU  - Lorenc, Ljubinka
AU  - Kalvoda, J
PY  - 2004
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2705
AB  - In the present paper, the preparation of 3β-hydroxy-17β-dimethyl- tert-butylsilyloxy-5-azaandrostane (15) in fourteen steps is described. B-nor-17-oxoandrost-5-en-3β-yl acetate (1) 1,2 was used as the starting material, which was transformed to the key intermediate of the synthesis, B-nor-17β-dimethyl-tert-butylsilyloxyandrost-4-en-3β-yl acetate (7).
PB  - Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Synthesis of 5-azaandrostane-3β,17β-diol protected at the 17β-hydroxyl group
VL  - 69
IS  - 11
SP  - 861
EP  - 869
DO  - 10.2298/JSC0411861P
ER  - 
@article{
author = "Pavlović, Vladimir D. and Dabović, Milan and Martinović, Saša B. and Lorenc, Ljubinka and Kalvoda, J",
year = "2004",
abstract = "In the present paper, the preparation of 3β-hydroxy-17β-dimethyl- tert-butylsilyloxy-5-azaandrostane (15) in fourteen steps is described. B-nor-17-oxoandrost-5-en-3β-yl acetate (1) 1,2 was used as the starting material, which was transformed to the key intermediate of the synthesis, B-nor-17β-dimethyl-tert-butylsilyloxyandrost-4-en-3β-yl acetate (7).",
publisher = "Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Synthesis of 5-azaandrostane-3β,17β-diol protected at the 17β-hydroxyl group",
volume = "69",
number = "11",
pages = "861-869",
doi = "10.2298/JSC0411861P"
}
Pavlović, V. D., Dabović, M., Martinović, S. B., Lorenc, L.,& Kalvoda, J.. (2004). Synthesis of 5-azaandrostane-3β,17β-diol protected at the 17β-hydroxyl group. in Journal of the Serbian Chemical Society
Serbian Chemical Society., 69(11), 861-869.
https://doi.org/10.2298/JSC0411861P
Pavlović VD, Dabović M, Martinović SB, Lorenc L, Kalvoda J. Synthesis of 5-azaandrostane-3β,17β-diol protected at the 17β-hydroxyl group. in Journal of the Serbian Chemical Society. 2004;69(11):861-869.
doi:10.2298/JSC0411861P .
Pavlović, Vladimir D., Dabović, Milan, Martinović, Saša B., Lorenc, Ljubinka, Kalvoda, J, "Synthesis of 5-azaandrostane-3β,17β-diol protected at the 17β-hydroxyl group" in Journal of the Serbian Chemical Society, 69, no. 11 (2004):861-869,
https://doi.org/10.2298/JSC0411861P . .
3
4
4