Kálai, Tamás and Bagi, Nárcisz and Jekő, József and Berente, Zoltán and Hideg, Kálmán (2010) Synthesis of new paramagnetic selenophenes. Synthesis-Stuttgart, 2010 (10). pp. 1702-1706. ISSN 0039-7881
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Official URL: https://www.thieme-connect.de/DOI/DOI?10.1055/s-00...
Abstract
Abstract: Starting from 3-bromo-4-formyl- or 3-bromo-4-cyano-2,2,5,5,-tetramethyl-2,5-dihydro-1H-pyrrol-1-yloxyl radicals, 2-substituted and 2,3-disubstituted 5H-selenolo[2,3-c]pyrrol-5-yloxylradicals were synthesized. The 2-(bromomethyl)-substituted 5H-selenolo[2,3-c]pyrrol-5-yloxyl derivative was a key intermediate in the synthesis of a thiol specific methanethiosulfonate spin label reagent, a paramagnetic, selenophene ring-containing amino acid, and a new quinazolin-4(3H)-one derivative.
Item Type: | Article |
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Subjects: | Q Science / természettudomány > QD Chemistry / kémia |
Depositing User: | Dr. Tamás Kálai |
Date Deposited: | 31 Jan 2012 05:26 |
Last Modified: | 31 Dec 2022 00:15 |
URI: | http://real.mtak.hu/id/eprint/2792 |
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