Preparative chemical methods for aromatization of 19-nor-delta 4-3-oxosteroids

Two preparative chemical methods for aromatization of 19-nor-delta 4-3-oxosteroids are described. The first method consists of an oxidative aromatization of 19-nor-delta 4-3-oxosteroids with iodine-ceric ammonium nitrate in methanol to give a mixture of 3-methoxy ring-A aromatized derivatives consis...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Steroids 1994-11, Vol.59 (11), p.621-627
Hauptverfasser: Rao, P N, Cessac, J W, Kim, H K
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 627
container_issue 11
container_start_page 621
container_title Steroids
container_volume 59
creator Rao, P N
Cessac, J W
Kim, H K
description Two preparative chemical methods for aromatization of 19-nor-delta 4-3-oxosteroids are described. The first method consists of an oxidative aromatization of 19-nor-delta 4-3-oxosteroids with iodine-ceric ammonium nitrate in methanol to give a mixture of 3-methoxy ring-A aromatized derivatives consisting of the desired product, the delta 9,11 derivative, the 6-oxo derivative as well as some ring-A iodinated material. Conversion of this material to a mixture of the 3-methoxy ring-A aromatized derivative and its 6-oxo derivative was achieved by catalytic hydrogenation. Finally, reduction of the 6-oxo function with triethylsilane in trifluoroacetic acid gave the 3-methoxy-17-trifluoroacetate ring-A aromatized derivative as a single product. In the second method, reaction of 19-nor-delta 4-3-oxosteroids with copper (II) bromide in acetonitrile at room temperature resulted in aromatic steroids in a single step in excellent yields. The second method was used in the first practical chemical synthesis of a 6-dehydroestrogen from a 19-nor-delta 4,6-3-oxosteroid.
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_77786770</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>77786770</sourcerecordid><originalsourceid>FETCH-LOGICAL-p537-e60fb434efe4a7811b6a31f43640f963cba4706a36818bc894f4fd7dd24e9f23</originalsourceid><addsrcrecordid>eNotT0tLxDAYzEFZ19WfIOTkLZA0MY-jLL5gUcE97K2kzRe20jQ1aUX99Qa2h2FgZphhztCaUm4Iq_ThAl3m_EkpldxUK7RSirI7rtbo9T3BaJOdum_A7RFC19oeB5iO0WXsY8I2xVDsv4I44OgxM2SIiTjoJ4sF4ST-xDxBip3LV-jc2z7D9cIb9PH4sN8-k93b08v2fkfGskpAUt8ILsCDsEoz1kjLmRdcCuqN5G1jhaJFk5rpptVGeOGdcq4SYHzFN-j21Dqm-DVDnurQ5Rb63g4Q51wrpbQsF0vwZgnOTQBXj6kLNv3Wy33-D6LOVX8</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>77786770</pqid></control><display><type>article</type><title>Preparative chemical methods for aromatization of 19-nor-delta 4-3-oxosteroids</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Rao, P N ; Cessac, J W ; Kim, H K</creator><creatorcontrib>Rao, P N ; Cessac, J W ; Kim, H K</creatorcontrib><description>Two preparative chemical methods for aromatization of 19-nor-delta 4-3-oxosteroids are described. The first method consists of an oxidative aromatization of 19-nor-delta 4-3-oxosteroids with iodine-ceric ammonium nitrate in methanol to give a mixture of 3-methoxy ring-A aromatized derivatives consisting of the desired product, the delta 9,11 derivative, the 6-oxo derivative as well as some ring-A iodinated material. Conversion of this material to a mixture of the 3-methoxy ring-A aromatized derivative and its 6-oxo derivative was achieved by catalytic hydrogenation. Finally, reduction of the 6-oxo function with triethylsilane in trifluoroacetic acid gave the 3-methoxy-17-trifluoroacetate ring-A aromatized derivative as a single product. In the second method, reaction of 19-nor-delta 4-3-oxosteroids with copper (II) bromide in acetonitrile at room temperature resulted in aromatic steroids in a single step in excellent yields. The second method was used in the first practical chemical synthesis of a 6-dehydroestrogen from a 19-nor-delta 4,6-3-oxosteroid.</description><identifier>ISSN: 0039-128X</identifier><identifier>PMID: 7701537</identifier><language>eng</language><publisher>United States</publisher><subject>Aromatase - metabolism ; Ketosteroids - chemistry ; Molecular Structure ; Oxidation-Reduction</subject><ispartof>Steroids, 1994-11, Vol.59 (11), p.621-627</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7701537$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rao, P N</creatorcontrib><creatorcontrib>Cessac, J W</creatorcontrib><creatorcontrib>Kim, H K</creatorcontrib><title>Preparative chemical methods for aromatization of 19-nor-delta 4-3-oxosteroids</title><title>Steroids</title><addtitle>Steroids</addtitle><description>Two preparative chemical methods for aromatization of 19-nor-delta 4-3-oxosteroids are described. The first method consists of an oxidative aromatization of 19-nor-delta 4-3-oxosteroids with iodine-ceric ammonium nitrate in methanol to give a mixture of 3-methoxy ring-A aromatized derivatives consisting of the desired product, the delta 9,11 derivative, the 6-oxo derivative as well as some ring-A iodinated material. Conversion of this material to a mixture of the 3-methoxy ring-A aromatized derivative and its 6-oxo derivative was achieved by catalytic hydrogenation. Finally, reduction of the 6-oxo function with triethylsilane in trifluoroacetic acid gave the 3-methoxy-17-trifluoroacetate ring-A aromatized derivative as a single product. In the second method, reaction of 19-nor-delta 4-3-oxosteroids with copper (II) bromide in acetonitrile at room temperature resulted in aromatic steroids in a single step in excellent yields. The second method was used in the first practical chemical synthesis of a 6-dehydroestrogen from a 19-nor-delta 4,6-3-oxosteroid.</description><subject>Aromatase - metabolism</subject><subject>Ketosteroids - chemistry</subject><subject>Molecular Structure</subject><subject>Oxidation-Reduction</subject><issn>0039-128X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNotT0tLxDAYzEFZ19WfIOTkLZA0MY-jLL5gUcE97K2kzRe20jQ1aUX99Qa2h2FgZphhztCaUm4Iq_ThAl3m_EkpldxUK7RSirI7rtbo9T3BaJOdum_A7RFC19oeB5iO0WXsY8I2xVDsv4I44OgxM2SIiTjoJ4sF4ST-xDxBip3LV-jc2z7D9cIb9PH4sN8-k93b08v2fkfGskpAUt8ILsCDsEoz1kjLmRdcCuqN5G1jhaJFk5rpptVGeOGdcq4SYHzFN-j21Dqm-DVDnurQ5Rb63g4Q51wrpbQsF0vwZgnOTQBXj6kLNv3Wy33-D6LOVX8</recordid><startdate>199411</startdate><enddate>199411</enddate><creator>Rao, P N</creator><creator>Cessac, J W</creator><creator>Kim, H K</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>199411</creationdate><title>Preparative chemical methods for aromatization of 19-nor-delta 4-3-oxosteroids</title><author>Rao, P N ; Cessac, J W ; Kim, H K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p537-e60fb434efe4a7811b6a31f43640f963cba4706a36818bc894f4fd7dd24e9f23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Aromatase - metabolism</topic><topic>Ketosteroids - chemistry</topic><topic>Molecular Structure</topic><topic>Oxidation-Reduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rao, P N</creatorcontrib><creatorcontrib>Cessac, J W</creatorcontrib><creatorcontrib>Kim, H K</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Steroids</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rao, P N</au><au>Cessac, J W</au><au>Kim, H K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preparative chemical methods for aromatization of 19-nor-delta 4-3-oxosteroids</atitle><jtitle>Steroids</jtitle><addtitle>Steroids</addtitle><date>1994-11</date><risdate>1994</risdate><volume>59</volume><issue>11</issue><spage>621</spage><epage>627</epage><pages>621-627</pages><issn>0039-128X</issn><abstract>Two preparative chemical methods for aromatization of 19-nor-delta 4-3-oxosteroids are described. The first method consists of an oxidative aromatization of 19-nor-delta 4-3-oxosteroids with iodine-ceric ammonium nitrate in methanol to give a mixture of 3-methoxy ring-A aromatized derivatives consisting of the desired product, the delta 9,11 derivative, the 6-oxo derivative as well as some ring-A iodinated material. Conversion of this material to a mixture of the 3-methoxy ring-A aromatized derivative and its 6-oxo derivative was achieved by catalytic hydrogenation. Finally, reduction of the 6-oxo function with triethylsilane in trifluoroacetic acid gave the 3-methoxy-17-trifluoroacetate ring-A aromatized derivative as a single product. In the second method, reaction of 19-nor-delta 4-3-oxosteroids with copper (II) bromide in acetonitrile at room temperature resulted in aromatic steroids in a single step in excellent yields. The second method was used in the first practical chemical synthesis of a 6-dehydroestrogen from a 19-nor-delta 4,6-3-oxosteroid.</abstract><cop>United States</cop><pmid>7701537</pmid><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0039-128X
ispartof Steroids, 1994-11, Vol.59 (11), p.621-627
issn 0039-128X
language eng
recordid cdi_proquest_miscellaneous_77786770
source MEDLINE; Elsevier ScienceDirect Journals
subjects Aromatase - metabolism
Ketosteroids - chemistry
Molecular Structure
Oxidation-Reduction
title Preparative chemical methods for aromatization of 19-nor-delta 4-3-oxosteroids
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-31T22%3A51%3A40IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Preparative%20chemical%20methods%20for%20aromatization%20of%2019-nor-delta%204-3-oxosteroids&rft.jtitle=Steroids&rft.au=Rao,%20P%20N&rft.date=1994-11&rft.volume=59&rft.issue=11&rft.spage=621&rft.epage=627&rft.pages=621-627&rft.issn=0039-128X&rft_id=info:doi/&rft_dat=%3Cproquest_pubme%3E77786770%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=77786770&rft_id=info:pmid/7701537&rfr_iscdi=true