Studies on Organometallic Compounds. II. Facile and Convenient Method for the Synthesis of Iodoazines through Iododestannation of Trimethylstannylazines
Trimethylstannyl and bis (trimethylstannyl) derivatives of pyridine, quinoline, and isoquinoline were prepared from the corresponding halo and dihalo (chloro or bromo) derivatives and trimethylstannyl sodium, which was generated in situ from chlorotrimethyl-stannane and sodium. These stannyl derivat...
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Veröffentlicht in: | Chemical & pharmaceutical bulletin 1982/05/25, Vol.30(5), pp.1731-1737 |
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container_title | Chemical & pharmaceutical bulletin |
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creator | YAMAMOTO, YUTAKA YANAGI, AKIHIKO |
description | Trimethylstannyl and bis (trimethylstannyl) derivatives of pyridine, quinoline, and isoquinoline were prepared from the corresponding halo and dihalo (chloro or bromo) derivatives and trimethylstannyl sodium, which was generated in situ from chlorotrimethyl-stannane and sodium. These stannyl derivatives readily underwent iododestannation on treatment with iodine to produce the corresponding iodo and diiodo derivatives of pyridine, quinoline, and isoquinoline, respectively, in good yields. |
doi_str_mv | 10.1248/cpb.30.1731 |
format | Article |
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These stannyl derivatives readily underwent iododestannation on treatment with iodine to produce the corresponding iodo and diiodo derivatives of pyridine, quinoline, and isoquinoline, respectively, in good yields.</description><subject>chlorotrimethylstannane</subject><issn>0009-2363</issn><issn>1347-5223</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1982</creationdate><recordtype>article</recordtype><recordid>eNpFkMlOwzAQhi0EEmU58QKWOKIUb9mOqGyVQBxazpHjOI2rYBfbQSpPwuMyIQguntHMN_8_HoQuKJlTJoprtavnHPKc0wM0o1zkScoYP0QzQkiZMJ7xY3QSwpYQlpKcz9DXKg6N0QE7i1_8Rlr3pqPse6Pwwr3t3GCbMMfL5RzfS2V6jaVtoGM_tDXaRvysY-ca3DqPY6fxam8hBAN6LV66xslPY0E9dt4Nm-6n1OgQpbUyGvAEbO0NeHb7_qe876eRM3TUyj7o8994il7v79aLx-Tp5WG5uHlKlMgympRcF6LWuq1VVjAmlGQZyWRKU85IIXKqCCP5eJCiloxRVTDeUsKkVHXd5IqfostJd-fd-wCrVVs3eAuWFRVpWQrKuADqaqKUdyF43VY72Fr6fUVJNZ6-gtNXHHJwAvp2orfwpY3-Y6WPRvV6ZGmZFiOfTs849t_upK-05d-p4pFJ</recordid><startdate>1982</startdate><enddate>1982</enddate><creator>YAMAMOTO, YUTAKA</creator><creator>YANAGI, AKIHIKO</creator><general>The Pharmaceutical Society of Japan</general><general>Japan Science and Technology Agency</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>H94</scope></search><sort><creationdate>1982</creationdate><title>Studies on Organometallic Compounds. 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Facile and Convenient Method for the Synthesis of Iodoazines through Iododestannation of Trimethylstannylazines</title><author>YAMAMOTO, YUTAKA ; YANAGI, AKIHIKO</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4661-93e84beefbc68224ca2606a5153208471c020717318ba221c823f102aacbbd7c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1982</creationdate><topic>chlorotrimethylstannane</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>YAMAMOTO, YUTAKA</creatorcontrib><creatorcontrib>YANAGI, AKIHIKO</creatorcontrib><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Chemical & pharmaceutical bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>YAMAMOTO, YUTAKA</au><au>YANAGI, AKIHIKO</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Studies on Organometallic Compounds. II. Facile and Convenient Method for the Synthesis of Iodoazines through Iododestannation of Trimethylstannylazines</atitle><jtitle>Chemical & pharmaceutical bulletin</jtitle><addtitle>Chem. Pharm. Bull.</addtitle><date>1982</date><risdate>1982</risdate><volume>30</volume><issue>5</issue><spage>1731</spage><epage>1737</epage><pages>1731-1737</pages><issn>0009-2363</issn><eissn>1347-5223</eissn><abstract>Trimethylstannyl and bis (trimethylstannyl) derivatives of pyridine, quinoline, and isoquinoline were prepared from the corresponding halo and dihalo (chloro or bromo) derivatives and trimethylstannyl sodium, which was generated in situ from chlorotrimethyl-stannane and sodium. These stannyl derivatives readily underwent iododestannation on treatment with iodine to produce the corresponding iodo and diiodo derivatives of pyridine, quinoline, and isoquinoline, respectively, in good yields.</abstract><cop>Tokyo</cop><pub>The Pharmaceutical Society of Japan</pub><doi>10.1248/cpb.30.1731</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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source | Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; J-STAGE (Japan Science & Technology Information Aggregator, Electronic) Freely Available Titles - Japanese; Free Full-Text Journals in Chemistry |
subjects | chlorotrimethylstannane |
title | Studies on Organometallic Compounds. II. Facile and Convenient Method for the Synthesis of Iodoazines through Iododestannation of Trimethylstannylazines |
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