1970
DOI: 10.1002/macp.1970.021360128
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Synthese und polymerisation eines vinylmonomeren der nucleobase thymin

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Cited by 10 publications
(9 citation statements)
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“…The mechanism and the scope of this reaction will be the subject of a future report. The propenoic acid derivative 13 was synthesized by the condensation of 5-formyluracil (12)56 with malonic acid, to give exclusively the trans isomer as evidenced by nmr data.…”
mentioning
confidence: 99%
“…The mechanism and the scope of this reaction will be the subject of a future report. The propenoic acid derivative 13 was synthesized by the condensation of 5-formyluracil (12)56 with malonic acid, to give exclusively the trans isomer as evidenced by nmr data.…”
mentioning
confidence: 99%
“…1, Nr. 1-5) werden in 0,5 M NaCl-0,Ol M Na2HPOa-Puffer (pH 6,8) einige Stunden geruhrt und in gequollenem Zustand in eine Chromatographiesaule gefullt. Die Saule wird anschlieljend solange rnit dem Puffer eluiert, bis im Eluat keine UV-aktiven Substanzen mehr nachzuweisen sind.…”
Section: Chromatographieunclassified
“…By Alois Haas, Hartmut Reinke, and Jurgen Sommerhoffl*l HaloformyI(perhaloa1kyl)-sulfanes ( I ) and -disulfanes (2) have not previously been described. Reactions of the haloformyl group, e.g.…”
Section: Halof Ormyl(perhaloalky1)-sulfanes and -Andsulfanest**]mentioning
confidence: 99%
“…Nomenclature [ * *I: ( l a ) : 1,3,5,7-tetramethyl-l,3,5,7-tetrasilatricyclo[3.3.1.13~7]decane; (2): 1,3,7,9,11,13-hexamethyl-1,3,5,7,9,11,13-heptasilahexacyclo[7.5.1.1~~~~.1~~~~.0~~~~.0~~~~~heptadecane; (3) : 3,7,11 ,13,15,17-hexarnethyl-l, 3,5,7,9,11,13,-15,17-enneasilaenneacyclo [9.7.l.llJ. 13,17.17,15.05,16.09,14.-09,20.013 918Idocosane; (4) : 3,7,11,17-tetramethy1-1, 3,5,7,9,11,-13,15,17,19decasilaundecacyclo I9.9.1 .1135.13 [**I Because of the complexity of the official nomenclature we suggest that these compounds be refered to as carborundanesin line with the-ideal structure of carborundum (zinc blende type).…”
mentioning
confidence: 99%