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- Publisher Website: 10.1002/anie.201404543
- Scopus: eid_2-s2.0-84904467152
- PMID: 24909452
- WOS: WOS:000339564800040
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Article: Gold-catalyzed direct hydrogenative coupling of nitroarenes to synthesize aromatic azo compounds
Title | Gold-catalyzed direct hydrogenative coupling of nitroarenes to synthesize aromatic azo compounds |
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Authors | |
Keywords | azo compounds reduction gold supported catalysts arenes |
Issue Date | 2014 |
Citation | Angewandte Chemie - International Edition, 2014, v. 53, n. 29, p. 7624-7628 How to Cite? |
Abstract | The azo linkage is a prominent chemical motif which has found numerous applications in materials science, pharmaceuticals, and agrochemicals. Described herein is a sustainable heterogeneous-gold-catalyzed synthesis of azo arenes. Available nitroarenes are deoxygenated and linked selectively by the formation of N-N bonds using molecular H without any external additives. As a result of a unique and remarkable synergy between the metal and support, a facile surface-mediated condensation of nitroso and hydroxylamine intermediates is enabled, and the desired transformation proceeds in a highly selective manner under mild reaction conditions. The protocol tolerates a large variety of functional groups and offers a general and versatile method for the environmentally friendly synthesis of symmetric or asymmetric aromatic azo compounds. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. 2 |
Persistent Identifier | http://hdl.handle.net/10722/299510 |
ISSN | 2023 Impact Factor: 16.1 2023 SCImago Journal Rankings: 5.300 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Liu, Xiang | - |
dc.contributor.author | Li, Hai Qian | - |
dc.contributor.author | Ye, Sen | - |
dc.contributor.author | Liu, Yong Mei | - |
dc.contributor.author | He, He Yong | - |
dc.contributor.author | Cao, Yong | - |
dc.date.accessioned | 2021-05-21T03:34:34Z | - |
dc.date.available | 2021-05-21T03:34:34Z | - |
dc.date.issued | 2014 | - |
dc.identifier.citation | Angewandte Chemie - International Edition, 2014, v. 53, n. 29, p. 7624-7628 | - |
dc.identifier.issn | 1433-7851 | - |
dc.identifier.uri | http://hdl.handle.net/10722/299510 | - |
dc.description.abstract | The azo linkage is a prominent chemical motif which has found numerous applications in materials science, pharmaceuticals, and agrochemicals. Described herein is a sustainable heterogeneous-gold-catalyzed synthesis of azo arenes. Available nitroarenes are deoxygenated and linked selectively by the formation of N-N bonds using molecular H without any external additives. As a result of a unique and remarkable synergy between the metal and support, a facile surface-mediated condensation of nitroso and hydroxylamine intermediates is enabled, and the desired transformation proceeds in a highly selective manner under mild reaction conditions. The protocol tolerates a large variety of functional groups and offers a general and versatile method for the environmentally friendly synthesis of symmetric or asymmetric aromatic azo compounds. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. 2 | - |
dc.language | eng | - |
dc.relation.ispartof | Angewandte Chemie - International Edition | - |
dc.subject | azo compounds | - |
dc.subject | reduction | - |
dc.subject | gold | - |
dc.subject | supported catalysts | - |
dc.subject | arenes | - |
dc.title | Gold-catalyzed direct hydrogenative coupling of nitroarenes to synthesize aromatic azo compounds | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1002/anie.201404543 | - |
dc.identifier.pmid | 24909452 | - |
dc.identifier.scopus | eid_2-s2.0-84904467152 | - |
dc.identifier.volume | 53 | - |
dc.identifier.issue | 29 | - |
dc.identifier.spage | 7624 | - |
dc.identifier.epage | 7628 | - |
dc.identifier.eissn | 1521-3773 | - |
dc.identifier.isi | WOS:000339564800040 | - |