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Synthesis of 5-azaandrostane-3β, 17β-diol protected at the 17-hydroxyl group
In the present paper, the preparation of 3?-hydroxy-17?-dimethyl-tert-butylsilyloxy- 5-azaandrostane (15) in fourteen steps is described. B-nor-17-oxoandrost- 5-en-3?-yl acetate (1)1,2 was used as the starting material, which was transformed to the key intermediate of the synthesis, B-nor-17?-dimeth...
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Published in: | Journal of the Serbian Chemical Society 2004, Vol.69 (11), p.861-869 |
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container_end_page | 869 |
container_issue | 11 |
container_start_page | 861 |
container_title | Journal of the Serbian Chemical Society |
container_volume | 69 |
creator | Pavlovic, Vladimir Dabovic, Milan Martinovic, Sasa Lorenc, Ljubinka Kalvoda, Jaroslav |
description | In the present paper, the preparation of 3?-hydroxy-17?-dimethyl-tert-butylsilyloxy- 5-azaandrostane (15) in fourteen steps is described. B-nor-17-oxoandrost- 5-en-3?-yl acetate (1)1,2 was used as the starting material, which was transformed to the key intermediate of the synthesis, B-nor-17?-dimethyl-tert-butylsilyloxyandrost- 4-en-3?-yl acetate (7).
U ovom radu je opisano dobijanje 3?-hidroksi-17?-dimetil-tert-butilsililoksi-5-azaandrostana (15) u 14 faza. Kao polazno jedinjenje upotrebljen je B-nor-17-oksoandrost- 5-en-3?-il-acetat (1) koji je transformisan u kljucni intermedijer sinteze, B-nor-17?-dimetil tert-butilsililoksiandrost-4-en-3?-il-acetat (7). |
doi_str_mv | 10.2298/JSC0411861P |
format | article |
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U ovom radu je opisano dobijanje 3?-hidroksi-17?-dimetil-tert-butilsililoksi-5-azaandrostana (15) u 14 faza. Kao polazno jedinjenje upotrebljen je B-nor-17-oksoandrost- 5-en-3?-il-acetat (1) koji je transformisan u kljucni intermedijer sinteze, B-nor-17?-dimetil tert-butilsililoksiandrost-4-en-3?-il-acetat (7).</description><identifier>ISSN: 0352-5139</identifier><identifier>EISSN: 1820-7421</identifier><identifier>DOI: 10.2298/JSC0411861P</identifier><language>eng</language><publisher>Serbian Chemical Society</publisher><subject>3β-hydroxy-17β-dimethyl-tert-butylsilyloxy-5-azaandrostane ; 5-azasteroids ; b-nor-17-oxoandrost-5-en-3-yl acetate</subject><ispartof>Journal of the Serbian Chemical Society, 2004, Vol.69 (11), p.861-869</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c181p-7cce14b91c0153abd83cac176713403640be343b0253e23734bf87b18955ae303</citedby><cites>FETCH-LOGICAL-c181p-7cce14b91c0153abd83cac176713403640be343b0253e23734bf87b18955ae303</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,4010,27904,27905,27906</link.rule.ids></links><search><creatorcontrib>Pavlovic, Vladimir</creatorcontrib><creatorcontrib>Dabovic, Milan</creatorcontrib><creatorcontrib>Martinovic, Sasa</creatorcontrib><creatorcontrib>Lorenc, Ljubinka</creatorcontrib><creatorcontrib>Kalvoda, Jaroslav</creatorcontrib><title>Synthesis of 5-azaandrostane-3β, 17β-diol protected at the 17-hydroxyl group</title><title>Journal of the Serbian Chemical Society</title><description>In the present paper, the preparation of 3?-hydroxy-17?-dimethyl-tert-butylsilyloxy- 5-azaandrostane (15) in fourteen steps is described. B-nor-17-oxoandrost- 5-en-3?-yl acetate (1)1,2 was used as the starting material, which was transformed to the key intermediate of the synthesis, B-nor-17?-dimethyl-tert-butylsilyloxyandrost- 4-en-3?-yl acetate (7).
U ovom radu je opisano dobijanje 3?-hidroksi-17?-dimetil-tert-butilsililoksi-5-azaandrostana (15) u 14 faza. Kao polazno jedinjenje upotrebljen je B-nor-17-oksoandrost- 5-en-3?-il-acetat (1) koji je transformisan u kljucni intermedijer sinteze, B-nor-17?-dimetil tert-butilsililoksiandrost-4-en-3?-il-acetat (7).</description><subject>3β-hydroxy-17β-dimethyl-tert-butylsilyloxy-5-azaandrostane</subject><subject>5-azasteroids</subject><subject>b-nor-17-oxoandrost-5-en-3-yl acetate</subject><issn>0352-5139</issn><issn>1820-7421</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpNkE1OwzAUhC0EEqWw4gLZg8Evz46dJar4KaoEqLCObMduU5U6coJE2HES7tCD9CpcgUARYjXSG82neUPIMbCzNM3V-e10xDiAyuB-hwxApYxKnsIuGTAUKRWA-T45aJoFY6kQyAfkYdqt2rlrqiYJPhFUv2m9KmNoWr1yFDfr0wTkZk3LKiyTOobW2daViW6TPtVbn-8fdN71gddumcxieKkPyZ7Xy8Yd_eqQPF1dPo5u6OTuejy6mFALCmoqrXXATQ6WgUBtSoVWW5CZBOQMM86MQ46mL4ouRYnceCUNqFwI7ZDhkIy33DLoRVHH6lnHrgi6Kn4OIc4KHdvKLl2hhCid9VJ7b3mmrcpKIbO-R2aE8cz1rJMty_afN9H5Px6w4nvZ4t-y-AVSSGx3</recordid><startdate>2004</startdate><enddate>2004</enddate><creator>Pavlovic, Vladimir</creator><creator>Dabovic, Milan</creator><creator>Martinovic, Sasa</creator><creator>Lorenc, Ljubinka</creator><creator>Kalvoda, Jaroslav</creator><general>Serbian Chemical Society</general><scope>AAYXX</scope><scope>CITATION</scope><scope>DOA</scope></search><sort><creationdate>2004</creationdate><title>Synthesis of 5-azaandrostane-3β, 17β-diol protected at the 17-hydroxyl group</title><author>Pavlovic, Vladimir ; Dabovic, Milan ; Martinovic, Sasa ; Lorenc, Ljubinka ; Kalvoda, Jaroslav</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c181p-7cce14b91c0153abd83cac176713403640be343b0253e23734bf87b18955ae303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>3β-hydroxy-17β-dimethyl-tert-butylsilyloxy-5-azaandrostane</topic><topic>5-azasteroids</topic><topic>b-nor-17-oxoandrost-5-en-3-yl acetate</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pavlovic, Vladimir</creatorcontrib><creatorcontrib>Dabovic, Milan</creatorcontrib><creatorcontrib>Martinovic, Sasa</creatorcontrib><creatorcontrib>Lorenc, Ljubinka</creatorcontrib><creatorcontrib>Kalvoda, Jaroslav</creatorcontrib><collection>CrossRef</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of the Serbian Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pavlovic, Vladimir</au><au>Dabovic, Milan</au><au>Martinovic, Sasa</au><au>Lorenc, Ljubinka</au><au>Kalvoda, Jaroslav</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of 5-azaandrostane-3β, 17β-diol protected at the 17-hydroxyl group</atitle><jtitle>Journal of the Serbian Chemical Society</jtitle><date>2004</date><risdate>2004</risdate><volume>69</volume><issue>11</issue><spage>861</spage><epage>869</epage><pages>861-869</pages><issn>0352-5139</issn><eissn>1820-7421</eissn><abstract>In the present paper, the preparation of 3?-hydroxy-17?-dimethyl-tert-butylsilyloxy- 5-azaandrostane (15) in fourteen steps is described. B-nor-17-oxoandrost- 5-en-3?-yl acetate (1)1,2 was used as the starting material, which was transformed to the key intermediate of the synthesis, B-nor-17?-dimethyl-tert-butylsilyloxyandrost- 4-en-3?-yl acetate (7).
U ovom radu je opisano dobijanje 3?-hidroksi-17?-dimetil-tert-butilsililoksi-5-azaandrostana (15) u 14 faza. Kao polazno jedinjenje upotrebljen je B-nor-17-oksoandrost- 5-en-3?-il-acetat (1) koji je transformisan u kljucni intermedijer sinteze, B-nor-17?-dimetil tert-butilsililoksiandrost-4-en-3?-il-acetat (7).</abstract><pub>Serbian Chemical Society</pub><doi>10.2298/JSC0411861P</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 3β-hydroxy-17β-dimethyl-tert-butylsilyloxy-5-azaandrostane 5-azasteroids b-nor-17-oxoandrost-5-en-3-yl acetate |
title | Synthesis of 5-azaandrostane-3β, 17β-diol protected at the 17-hydroxyl group |
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