Potent triazine-based dehydrocondensing reagents substituted by an amido group
書誌事項
- 公開日
- 2016-08-24
- 資源種別
- journal article
- 権利情報
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- http://creativecommons.org/licenses/by/4.0
- http://creativecommons.org/licenses/by/4.0
- http://creativecommons.org/licenses/by/4.0
- DOI
-
- 10.3762/bjoc.12.179
- 10.1002/chin.201649057
- 公開者
- Beilstein Institut
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説明
<jats:p>This study describes the synthesis of triazine-based dehydrocondensing reagents substituted by amido substituents and demonstrates their efficiency for dehydrocondensing reactions in MeOH and THF. <jats:italic>N</jats:italic>-Phenylbenzamido-substituted chlorotriazine is readily converted to a stable, non-hygroscopic triazinylammonium-based dehydrocondensing reagent that is superior to 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (DMT-MM) in terms of its reactivity in dehydrocondensing reactions.</jats:p>
収録刊行物
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- Beilstein Journal of Organic Chemistry
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Beilstein Journal of Organic Chemistry 12 1897-1903, 2016-08-24
Beilstein Institut
