4,6‐Diphenyl‐1‐(phenylsulfonyl)‐1H‐furo[3,4‐b]pyrrole
The title molecule, C24H17NO3S, is the first example of the 1H‐furo[3,4‐b]pyrrole ring system to be described. It crystallizes with three molecules in the asymmetric unit. In each molecule, the fused heterocycle is planar and one of the two phenyl groups on the furan ring is only slightly out of...
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Veröffentlicht in: | Acta crystallographica. Section E, Structure reports online Structure reports online, 2007-03, Vol.63 (3), p.o1279-o1281 |
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container_title | Acta crystallographica. Section E, Structure reports online |
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creator | Moskalev, Nikolai V. Gribble, Gordon W. Jasinski, Jerry P. |
description | The title molecule, C24H17NO3S, is the first example of the 1H‐furo[3,4‐b]pyrrole ring system to be described. It crystallizes with three molecules in the asymmetric unit. In each molecule, the fused heterocycle is planar and one of the two phenyl groups on the furan ring is only slightly out of planarity with the furan ring, while the other phenyl group is significantly twisted by 47.6 (4), 48.3 (3) and 54.1 (3)°. |
doi_str_mv | 10.1107/S1600536807005764 |
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Section E, Structure reports online</title><description>The title molecule, C24H17NO3S, is the first example of the 1H‐furo[3,4‐b]pyrrole ring system to be described. It crystallizes with three molecules in the asymmetric unit. In each molecule, the fused heterocycle is planar and one of the two phenyl groups on the furan ring is only slightly out of planarity with the furan ring, while the other phenyl group is significantly twisted by 47.6 (4), 48.3 (3) and 54.1 (3)°.</description><issn>1600-5368</issn><issn>1600-5368</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNplkF9Kw0AQxhdRsFYP4A0UGjuz_5I-1hptoeCDf0BEluxmFyNrE7IUyZtH8CK9RI_iSdxQHwQfZr7ffAPD8BFyinCBCOn4DiWAYDKDNGoq-R4Z9FbSe_t_-JAchfAGgDKlOCA5H8nvz6-rqnm1q85HxFhnu2m7CWvv6tV20_nzfjWPza3b-pmNeET90nRtW3t7TA5c4YM9-dUhebjO72fzZHl7s5hNl0mgIESCKNjEGW5FSY0sIdNOaydBF6xkQqI1mArg0gpWmv5Z6pAh6qxgxmBB2ZBMdnc_Km871bTVe9F2CkH1Iah_IajpU04vHylwwX4ARKtXkw</recordid><startdate>200703</startdate><enddate>200703</enddate><creator>Moskalev, Nikolai V.</creator><creator>Gribble, Gordon W.</creator><creator>Jasinski, Jerry P.</creator><general>Blackwell Publishing Ltd</general><scope/></search><sort><creationdate>200703</creationdate><title>4,6‐Diphenyl‐1‐(phenylsulfonyl)‐1H‐furo[3,4‐b]pyrrole</title><author>Moskalev, Nikolai V. ; Gribble, Gordon W. ; Jasinski, Jerry P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-s2055-11539fc4e5d2c6d08bfbbf60ba3d3561ec175046e53dc53682f1311b8a3cc1a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Moskalev, Nikolai V.</creatorcontrib><creatorcontrib>Gribble, Gordon W.</creatorcontrib><creatorcontrib>Jasinski, Jerry P.</creatorcontrib><jtitle>Acta crystallographica. Section E, Structure reports online</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moskalev, Nikolai V.</au><au>Gribble, Gordon W.</au><au>Jasinski, Jerry P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>4,6‐Diphenyl‐1‐(phenylsulfonyl)‐1H‐furo[3,4‐b]pyrrole</atitle><jtitle>Acta crystallographica. Section E, Structure reports online</jtitle><date>2007-03</date><risdate>2007</risdate><volume>63</volume><issue>3</issue><spage>o1279</spage><epage>o1281</epage><pages>o1279-o1281</pages><issn>1600-5368</issn><eissn>1600-5368</eissn><abstract>The title molecule, C24H17NO3S, is the first example of the 1H‐furo[3,4‐b]pyrrole ring system to be described. It crystallizes with three molecules in the asymmetric unit. In each molecule, the fused heterocycle is planar and one of the two phenyl groups on the furan ring is only slightly out of planarity with the furan ring, while the other phenyl group is significantly twisted by 47.6 (4), 48.3 (3) and 54.1 (3)°.</abstract><cop>5 Abbey Square, Chester, Cheshire CH1 2HU, England</cop><pub>Blackwell Publishing Ltd</pub><doi>10.1107/S1600536807005764</doi></addata></record> |
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source | Wiley Online Library Journals Frontfile Complete; Free Full-Text Journals in Chemistry |
title | 4,6‐Diphenyl‐1‐(phenylsulfonyl)‐1H‐furo[3,4‐b]pyrrole |
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