2-Bromo-N-(p-toluenesulfonyl)pyrrole: A Robust Derivative of 2-Bromopyrrole
Abstract 2-Bromo-N-(P-toluenesulfonyl)pyrrole (2), a crystalline stable derivative of 2-bromopyrrole (1) has been prepared in 80% yield by bromination of pyrrole, followed by conversion to the N-(P-toluenesulfonyl) derivative. This compound is stable indefinitely at ambient temperature. Compound 2 i...
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| Veröffentlicht in: | Synlett 2003-10, Vol.2003 (13), p.1993-1996 |
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| Hauptverfasser: | , , |
| Format: | Artikel |
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| container_end_page | 1996 |
|---|---|
| container_issue | 13 |
| container_start_page | 1993 |
| container_title | Synlett |
| container_volume | 2003 |
| creator | Knight, Lea W. Huffman, John W. Isherwood, Matthew L. |
| description | Abstract
2-Bromo-N-(P-toluenesulfonyl)pyrrole (2), a crystalline stable derivative of 2-bromopyrrole (1) has been prepared in 80% yield by bromination of pyrrole, followed by conversion to the N-(P-toluenesulfonyl) derivative. This compound is stable indefinitely at ambient temperature. Compound 2 is an excellent substrate for Suzuki coupling with arylboronic acids. |
| doi_str_mv | 10.1055/s-2003-42036 |
| format | Article |
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2-Bromo-N-(P-toluenesulfonyl)pyrrole (2), a crystalline stable derivative of 2-bromopyrrole (1) has been prepared in 80% yield by bromination of pyrrole, followed by conversion to the N-(P-toluenesulfonyl) derivative. This compound is stable indefinitely at ambient temperature. Compound 2 is an excellent substrate for Suzuki coupling with arylboronic acids.</description><identifier>ISSN: 0936-5214</identifier><identifier>EISSN: 1437-2096</identifier><identifier>DOI: 10.1055/s-2003-42036</identifier><language>eng</language><subject>letter</subject><ispartof>Synlett, 2003-10, Vol.2003 (13), p.1993-1996</ispartof><rights>Georg Thieme Verlag Stuttgart · New York</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c269t-a0137cbe0dcd143f3e021775841cb4abec0b4c95e85cd86eb4d974fe5b5af8b53</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-2003-42036.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1055/s-2003-42036$$EHTML$$P50$$Gthieme$$H</linktohtml><link.rule.ids>314,776,780,3004,3005,27901,27902,54534,54535</link.rule.ids></links><search><creatorcontrib>Knight, Lea W.</creatorcontrib><creatorcontrib>Huffman, John W.</creatorcontrib><creatorcontrib>Isherwood, Matthew L.</creatorcontrib><title>2-Bromo-N-(p-toluenesulfonyl)pyrrole: A Robust Derivative of 2-Bromopyrrole</title><title>Synlett</title><addtitle>Synlett</addtitle><description>Abstract
2-Bromo-N-(P-toluenesulfonyl)pyrrole (2), a crystalline stable derivative of 2-bromopyrrole (1) has been prepared in 80% yield by bromination of pyrrole, followed by conversion to the N-(P-toluenesulfonyl) derivative. This compound is stable indefinitely at ambient temperature. Compound 2 is an excellent substrate for Suzuki coupling with arylboronic acids.</description><subject>letter</subject><issn>0936-5214</issn><issn>1437-2096</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNptkEtLw0AUhQdRsFZ3_oAsFR2988rDXa1PLAqi6yEzuYMpaSbMJIX-e1PbpasDh-9eDh8h5wxuGCh1GykHEFRyEOkBmTApsrEp0kMygUKkVHEmj8lJjEsAJvMCJuSN0_vgV56-04uO9r4ZsMU4NM63m-ay24TgG7xLZsmnN0PskwcM9brs6zUm3iX74z12So5c2UQ82-eUfD89fs1f6OLj-XU-W1DL06KnJTCRWYNQ2Wqc6AQCZ1mmcsmskaVBC0baQmGubJWnaGRVZNKhMqp0uVFiSq53f23wMQZ0ugv1qgwbzUBvReiotyL0n4gRv9rh_U-NK9RLP4R23Pc__QtIKF6N</recordid><startdate>20031016</startdate><enddate>20031016</enddate><creator>Knight, Lea W.</creator><creator>Huffman, John W.</creator><creator>Isherwood, Matthew L.</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20031016</creationdate><title>2-Bromo-N-(p-toluenesulfonyl)pyrrole: A Robust Derivative of 2-Bromopyrrole</title><author>Knight, Lea W. ; Huffman, John W. ; Isherwood, Matthew L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c269t-a0137cbe0dcd143f3e021775841cb4abec0b4c95e85cd86eb4d974fe5b5af8b53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>letter</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Knight, Lea W.</creatorcontrib><creatorcontrib>Huffman, John W.</creatorcontrib><creatorcontrib>Isherwood, Matthew L.</creatorcontrib><collection>CrossRef</collection><jtitle>Synlett</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Knight, Lea W.</au><au>Huffman, John W.</au><au>Isherwood, Matthew L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>2-Bromo-N-(p-toluenesulfonyl)pyrrole: A Robust Derivative of 2-Bromopyrrole</atitle><jtitle>Synlett</jtitle><addtitle>Synlett</addtitle><date>2003-10-16</date><risdate>2003</risdate><volume>2003</volume><issue>13</issue><spage>1993</spage><epage>1996</epage><pages>1993-1996</pages><issn>0936-5214</issn><eissn>1437-2096</eissn><abstract>Abstract
2-Bromo-N-(P-toluenesulfonyl)pyrrole (2), a crystalline stable derivative of 2-bromopyrrole (1) has been prepared in 80% yield by bromination of pyrrole, followed by conversion to the N-(P-toluenesulfonyl) derivative. This compound is stable indefinitely at ambient temperature. Compound 2 is an excellent substrate for Suzuki coupling with arylboronic acids.</abstract><doi>10.1055/s-2003-42036</doi><tpages>4</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0936-5214 |
| ispartof | Synlett, 2003-10, Vol.2003 (13), p.1993-1996 |
| issn | 0936-5214 1437-2096 |
| language | eng |
| recordid | cdi_crossref_primary_10_1055_s_2003_42036 |
| source | Thieme Connect Journals |
| subjects | letter |
| title | 2-Bromo-N-(p-toluenesulfonyl)pyrrole: A Robust Derivative of 2-Bromopyrrole |
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