Sulfonamides derived from 1-hydroxy-6-aminonaphthalene-3-sulfonic acid (J acid)
The sulfonamides have the formula where R1 is C1-C13-lkyl, substituted or unsubstituted phenyl, C1-C8-alkanoyl or substituted or unsubstituted benzoyl, and R2 and R3 are each independently of one another substituted or unsubstituted C1-C13-alkyl, substituted or unsubstituted C5-C7-cycloalkyl or subs...
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creator | SCHLOESSER ULRIKE MAYER UDO |
description | The sulfonamides have the formula where R1 is C1-C13-lkyl, substituted or unsubstituted phenyl, C1-C8-alkanoyl or substituted or unsubstituted benzoyl, and R2 and R3 are each independently of one another substituted or unsubstituted C1-C13-alkyl, substituted or unsubstituted C5-C7-cycloalkyl or substituted or unsubstituted piperidinyt, or R2 may also be hydrogen.
The sulfonamides have the formula where R1 is C1-C13-lkyl, substituted or unsubstituted phenyl, C1-C8-alkanoyl or substituted or unsubstituted benzoyl, and R2 and R3 are each independently of one another substituted or unsubstituted C1-C13-alkyl, substituted or unsubstituted C5-C7-cycloalkyl or substituted or unsubstituted piperidinyt, or R2 may also be hydrogen. |
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The sulfonamides have the formula where R1 is C1-C13-lkyl, substituted or unsubstituted phenyl, C1-C8-alkanoyl or substituted or unsubstituted benzoyl, and R2 and R3 are each independently of one another substituted or unsubstituted C1-C13-alkyl, substituted or unsubstituted C5-C7-cycloalkyl or substituted or unsubstituted piperidinyt, or R2 may also be hydrogen.</description><edition>5</edition><language>eng</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>1994</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19941011&DB=EPODOC&CC=US&NR=5354904A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19941011&DB=EPODOC&CC=US&NR=5354904A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>SCHLOESSER; ULRIKE</creatorcontrib><creatorcontrib>MAYER; UDO</creatorcontrib><title>Sulfonamides derived from 1-hydroxy-6-aminonaphthalene-3-sulfonic acid (J acid)</title><description>The sulfonamides have the formula where R1 is C1-C13-lkyl, substituted or unsubstituted phenyl, C1-C8-alkanoyl or substituted or unsubstituted benzoyl, and R2 and R3 are each independently of one another substituted or unsubstituted C1-C13-alkyl, substituted or unsubstituted C5-C7-cycloalkyl or substituted or unsubstituted piperidinyt, or R2 may also be hydrogen.
The sulfonamides have the formula where R1 is C1-C13-lkyl, substituted or unsubstituted phenyl, C1-C8-alkanoyl or substituted or unsubstituted benzoyl, and R2 and R3 are each independently of one another substituted or unsubstituted C1-C13-alkyl, substituted or unsubstituted C5-C7-cycloalkyl or substituted or unsubstituted piperidinyt, or R2 may also be hydrogen.</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1994</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZPAPLs1Jy89LzM1MSS1WSEktyixLTVFIK8rPVTDUzahMKcqvqNQ10wXK5wFVFWSUZCTmpOal6hrrFoM1ZiYrJCZnpihoeIFpTR4G1rTEnOJUXijNzSDv5hri7KGbWpAfn1pckJgM1F0SHxpsamxqYmlg4mhMWAUAIoU1Kw</recordid><startdate>19941011</startdate><enddate>19941011</enddate><creator>SCHLOESSER; ULRIKE</creator><creator>MAYER; UDO</creator><scope>EVB</scope></search><sort><creationdate>19941011</creationdate><title>Sulfonamides derived from 1-hydroxy-6-aminonaphthalene-3-sulfonic acid (J acid)</title><author>SCHLOESSER; ULRIKE ; MAYER; UDO</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_US5354904A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1994</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>SCHLOESSER; ULRIKE</creatorcontrib><creatorcontrib>MAYER; UDO</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>SCHLOESSER; ULRIKE</au><au>MAYER; UDO</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Sulfonamides derived from 1-hydroxy-6-aminonaphthalene-3-sulfonic acid (J acid)</title><date>1994-10-11</date><risdate>1994</risdate><abstract>The sulfonamides have the formula where R1 is C1-C13-lkyl, substituted or unsubstituted phenyl, C1-C8-alkanoyl or substituted or unsubstituted benzoyl, and R2 and R3 are each independently of one another substituted or unsubstituted C1-C13-alkyl, substituted or unsubstituted C5-C7-cycloalkyl or substituted or unsubstituted piperidinyt, or R2 may also be hydrogen.
The sulfonamides have the formula where R1 is C1-C13-lkyl, substituted or unsubstituted phenyl, C1-C8-alkanoyl or substituted or unsubstituted benzoyl, and R2 and R3 are each independently of one another substituted or unsubstituted C1-C13-alkyl, substituted or unsubstituted C5-C7-cycloalkyl or substituted or unsubstituted piperidinyt, or R2 may also be hydrogen.</abstract><edition>5</edition><oa>free_for_read</oa></addata></record> |
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subjects | ACYCLIC OR CARBOCYCLIC COMPOUNDS CHEMISTRY HETEROCYCLIC COMPOUNDS METALLURGY ORGANIC CHEMISTRY |
title | Sulfonamides derived from 1-hydroxy-6-aminonaphthalene-3-sulfonic acid (J acid) |
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