Enthalogenierung von Bis(diisopropylamino-chlorboryl)methan: Lösungsmittelabhängige Bildung eines 1,2,4,5-Tetraborinan-und eines 1-Aza-2,4-diborolidin-Derivats / Dehalogenation of Bis(diisopropylamino-chloroboryl)methane: Solvent-dependent Formation of a 1,2,4,5-Tetraborinane and of a 1-Aza-2,4-diborolidine Derivative
Dehalogenation of bis(diisopropylamino-chloroboryl)methane 1 b with sodium/potassium alloy in petroleum ether yields the 1,2,4,5-tetraborinane 2b (38%), whereas in tetrahydrofuran the five-membered 1-aza-2,4-diborolidine derivative 3a (36%) is formed. The constitution of 2b and 3a follows from spect...
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Veröffentlicht in: | Zeitschrift für Naturforschung. B, A journal of chemical sciences A journal of chemical sciences, 1988-06, Vol.43 (6), p.658-664 |
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container_title | Zeitschrift für Naturforschung. B, A journal of chemical sciences |
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creator | Fisch, Herbert Pritzkow, Hans Siebert, Walter |
description | Dehalogenation of bis(diisopropylamino-chloroboryl)methane 1 b with sodium/potassium alloy in petroleum ether yields the 1,2,4,5-tetraborinane 2b (38%), whereas in tetrahydrofuran the five-membered 1-aza-2,4-diborolidine derivative 3a (36%) is formed. The constitution of 2b and 3a follows from spectroscopic data and has been confirmed by X-ray structure analyses. |
doi_str_mv | 10.1515/znb-1988-0604 |
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The constitution of 2b and 3a follows from spectroscopic data and has been confirmed by X-ray structure analyses.</description><subject>1-Aza-2</subject><subject>4-diborolidine Derivatives</subject><subject>5-tetraborinane</subject><subject>5-Tetrakis(diisopropylamino-chloroboryl)-1</subject><issn>0932-0776</issn><issn>1865-7117</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><recordid>eNp9kU9r2zAYxr2yQbN2x911XCFapViW7O6UJu1WCOyw9mxk67WjIktBslOSz7PPsC_QLzaFpKWH0NP7wvOHHzxJ8pWS7zSj2eXWVpgWeY4JJ-wkGdGcZ1hQKj4mI1KkE0yE4KfJ5xAeCaEFY2T0YXpj-6U0rgWrwQ-2RWtn0bUO35TWwa28W22M7LR1uF4a5yvnN-aigxiyV2jx_C_ETOh034OR1fL5r211C7HAqF0ZaAsB0fFkzMYZvofey9igrbR4sOpFxtOtxNGClY6qM1ppi-fg9Vr2AV2iORwQZa8jnWveAXRvCeEK_XFmDbbHClZgVfzQrfPda5E8CgdIRrq9fAwO0IFOr-E8-dRIE-DL4Z4lD7c397NfePH7591susD1JC1yXAmVCQ5Vw7KUC6loowgvCGGVpLRmVdypLmqWEkpyEE1ORcXSgglOMiAFU-lZgve9tXcheGjKlded9JuSknK3fxn3L3f7l7v9o__H3v8kTQ9eQeuHTXzKRzd4G0mP51jKeZan_wF5v74j</recordid><startdate>19880601</startdate><enddate>19880601</enddate><creator>Fisch, Herbert</creator><creator>Pritzkow, Hans</creator><creator>Siebert, Walter</creator><general>Verlag der Zeitschrift für Naturforschung</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19880601</creationdate><title>Enthalogenierung von Bis(diisopropylamino-chlorboryl)methan: Lösungsmittelabhängige Bildung eines 1,2,4,5-Tetraborinan-und eines 1-Aza-2,4-diborolidin-Derivats / Dehalogenation of Bis(diisopropylamino-chloroboryl)methane: Solvent-dependent Formation of a 1,2,4,5-Tetraborinane and of a 1-Aza-2,4-diborolidine Derivative</title><author>Fisch, Herbert ; Pritzkow, Hans ; Siebert, Walter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2398-b7d576ebf45367ad1fd069004ba11c4b711c9c430108e7f817b43947605e094d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>1-Aza-2</topic><topic>4-diborolidine Derivatives</topic><topic>5-tetraborinane</topic><topic>5-Tetrakis(diisopropylamino-chloroboryl)-1</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fisch, Herbert</creatorcontrib><creatorcontrib>Pritzkow, Hans</creatorcontrib><creatorcontrib>Siebert, Walter</creatorcontrib><collection>CrossRef</collection><jtitle>Zeitschrift für Naturforschung. 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B, A journal of chemical sciences</jtitle><date>1988-06-01</date><risdate>1988</risdate><volume>43</volume><issue>6</issue><spage>658</spage><epage>664</epage><pages>658-664</pages><issn>0932-0776</issn><eissn>1865-7117</eissn><abstract>Dehalogenation of bis(diisopropylamino-chloroboryl)methane 1 b with sodium/potassium alloy in petroleum ether yields the 1,2,4,5-tetraborinane 2b (38%), whereas in tetrahydrofuran the five-membered 1-aza-2,4-diborolidine derivative 3a (36%) is formed. The constitution of 2b and 3a follows from spectroscopic data and has been confirmed by X-ray structure analyses.</abstract><pub>Verlag der Zeitschrift für Naturforschung</pub><doi>10.1515/znb-1988-0604</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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issn | 0932-0776 1865-7117 |
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source | Alma/SFX Local Collection |
subjects | 1-Aza-2 4-diborolidine Derivatives 5-tetraborinane 5-Tetrakis(diisopropylamino-chloroboryl)-1 |
title | Enthalogenierung von Bis(diisopropylamino-chlorboryl)methan: Lösungsmittelabhängige Bildung eines 1,2,4,5-Tetraborinan-und eines 1-Aza-2,4-diborolidin-Derivats / Dehalogenation of Bis(diisopropylamino-chloroboryl)methane: Solvent-dependent Formation of a 1,2,4,5-Tetraborinane and of a 1-Aza-2,4-diborolidine Derivative |
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