A novel method for the synthesis of maxacalcitol
Maxacalcitol ( 1 ), a kind of active vitamin D drugs, was prepared from pregnenolone acetate ( 2 ) using a novel synthetic method including the combination of five-step organic transformations and one-step biological transformation. The new protocol was shorter, milder, and simpler than the reported...
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Veröffentlicht in: | Russian journal of general chemistry 2016, Vol.86 (1), p.173-177 |
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container_title | Russian journal of general chemistry |
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creator | Song, W.-Q. Wang, Y.-H. Liu, D.-N. Fang, W.-Z. Lu, Q. |
description | Maxacalcitol (
1
), a kind of active vitamin D drugs, was prepared from pregnenolone acetate (
2
) using a novel synthetic method including the combination of five-step organic transformations and one-step biological transformation. The new protocol was shorter, milder, and simpler than the reported approaches. The unoptimized overall yield was 0.178%. The structure of all intermediates and final product was confirmed by
1
H NMR,
13
C NMR and MS techniques. |
doi_str_mv | 10.1134/S1070363216010278 |
format | Article |
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1
), a kind of active vitamin D drugs, was prepared from pregnenolone acetate (
2
) using a novel synthetic method including the combination of five-step organic transformations and one-step biological transformation. The new protocol was shorter, milder, and simpler than the reported approaches. The unoptimized overall yield was 0.178%. The structure of all intermediates and final product was confirmed by
1
H NMR,
13
C NMR and MS techniques.</description><identifier>ISSN: 1070-3632</identifier><identifier>EISSN: 1608-3350</identifier><identifier>DOI: 10.1134/S1070363216010278</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>Chemistry ; Chemistry and Materials Science ; Chemistry/Food Science</subject><ispartof>Russian journal of general chemistry, 2016, Vol.86 (1), p.173-177</ispartof><rights>Pleiades Publishing, Ltd. 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c288t-4661adbe966cd71b3b4a2971a150b568107623fc3a54f3e3f6b0ff5cb626cb8c3</citedby><cites>FETCH-LOGICAL-c288t-4661adbe966cd71b3b4a2971a150b568107623fc3a54f3e3f6b0ff5cb626cb8c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1134/S1070363216010278$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1134/S1070363216010278$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>315,781,785,27929,27930,41493,42562,51324</link.rule.ids></links><search><creatorcontrib>Song, W.-Q.</creatorcontrib><creatorcontrib>Wang, Y.-H.</creatorcontrib><creatorcontrib>Liu, D.-N.</creatorcontrib><creatorcontrib>Fang, W.-Z.</creatorcontrib><creatorcontrib>Lu, Q.</creatorcontrib><title>A novel method for the synthesis of maxacalcitol</title><title>Russian journal of general chemistry</title><addtitle>Russ J Gen Chem</addtitle><description>Maxacalcitol (
1
), a kind of active vitamin D drugs, was prepared from pregnenolone acetate (
2
) using a novel synthetic method including the combination of five-step organic transformations and one-step biological transformation. The new protocol was shorter, milder, and simpler than the reported approaches. The unoptimized overall yield was 0.178%. The structure of all intermediates and final product was confirmed by
1
H NMR,
13
C NMR and MS techniques.</description><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chemistry/Food Science</subject><issn>1070-3632</issn><issn>1608-3350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp9T8tKAzEUDaJgbf0Ad_mB0XuTmTvpshRfUHChXQ9JJrFTZiaSjGL_3pS6E1ydA-fBOYzdINwiyvLuFaEGSVIgAYKo1RmbZaoKKSs4zzzLxVG_ZFcp7SGbgMSMwYqP4cv1fHDTLrTch8innePpMGZIXeLB80F_a6t7202hX7ALr_vkrn9xzrYP92_rp2Lz8vi8Xm0KK5SaipIIdWvcksi2NRppSi2WNWqswFSk8h4S0lupq9JLJz0Z8L6yhgRZo6ycMzz12hhSis43H7EbdDw0CM3xcvPncs6IUyZl7_juYrMPn3HMM_8J_QAGVlcx</recordid><startdate>2016</startdate><enddate>2016</enddate><creator>Song, W.-Q.</creator><creator>Wang, Y.-H.</creator><creator>Liu, D.-N.</creator><creator>Fang, W.-Z.</creator><creator>Lu, Q.</creator><general>Pleiades Publishing</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>2016</creationdate><title>A novel method for the synthesis of maxacalcitol</title><author>Song, W.-Q. ; Wang, Y.-H. ; Liu, D.-N. ; Fang, W.-Z. ; Lu, Q.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c288t-4661adbe966cd71b3b4a2971a150b568107623fc3a54f3e3f6b0ff5cb626cb8c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Chemistry/Food Science</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Song, W.-Q.</creatorcontrib><creatorcontrib>Wang, Y.-H.</creatorcontrib><creatorcontrib>Liu, D.-N.</creatorcontrib><creatorcontrib>Fang, W.-Z.</creatorcontrib><creatorcontrib>Lu, Q.</creatorcontrib><collection>CrossRef</collection><jtitle>Russian journal of general chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Song, W.-Q.</au><au>Wang, Y.-H.</au><au>Liu, D.-N.</au><au>Fang, W.-Z.</au><au>Lu, Q.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A novel method for the synthesis of maxacalcitol</atitle><jtitle>Russian journal of general chemistry</jtitle><stitle>Russ J Gen Chem</stitle><date>2016</date><risdate>2016</risdate><volume>86</volume><issue>1</issue><spage>173</spage><epage>177</epage><pages>173-177</pages><issn>1070-3632</issn><eissn>1608-3350</eissn><abstract>Maxacalcitol (
1
), a kind of active vitamin D drugs, was prepared from pregnenolone acetate (
2
) using a novel synthetic method including the combination of five-step organic transformations and one-step biological transformation. The new protocol was shorter, milder, and simpler than the reported approaches. The unoptimized overall yield was 0.178%. The structure of all intermediates and final product was confirmed by
1
H NMR,
13
C NMR and MS techniques.</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><doi>10.1134/S1070363216010278</doi><tpages>5</tpages></addata></record> |
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subjects | Chemistry Chemistry and Materials Science Chemistry/Food Science |
title | A novel method for the synthesis of maxacalcitol |
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