{"title":"使用Pt/SiO2催化剂和低压氢气,通过氢化NAD+类似物进行高选择性1,4- nadh再生。","authors":"Makoto Hirano, Wataru Onodera, Masazumi Tamura, Yutaka Amao","doi":"10.1039/d5cc04253d","DOIUrl":null,"url":null,"abstract":"<p><p>The hydrogenation of nicotinamide analogs using a Pt/SiO<sub>2</sub> catalyst, followed by hydride transfer to NAD<sup>+</sup>, results in the highly selective regeneration of 1,4-NADH. <i>N</i>-Methyl nicotinamide exhibits the highest reactivity, achieving 98% selectivity at 20 °C under 1 atm H<sub>2</sub>. This strategy provides a practical and sustainable pathway for 1,4-NADH regeneration.</p>","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":" ","pages":""},"PeriodicalIF":4.2000,"publicationDate":"2025-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Highly selective 1,4-NADH regeneration <i>via</i> hydrogenated NAD<sup>+</sup> analogs using a Pt/SiO<sub>2</sub> catalyst with low pressure hydrogen gas.\",\"authors\":\"Makoto Hirano, Wataru Onodera, Masazumi Tamura, Yutaka Amao\",\"doi\":\"10.1039/d5cc04253d\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The hydrogenation of nicotinamide analogs using a Pt/SiO<sub>2</sub> catalyst, followed by hydride transfer to NAD<sup>+</sup>, results in the highly selective regeneration of 1,4-NADH. <i>N</i>-Methyl nicotinamide exhibits the highest reactivity, achieving 98% selectivity at 20 °C under 1 atm H<sub>2</sub>. This strategy provides a practical and sustainable pathway for 1,4-NADH regeneration.</p>\",\"PeriodicalId\":67,\"journal\":{\"name\":\"Chemical Communications\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-09-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Communications\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d5cc04253d\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Communications","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5cc04253d","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Highly selective 1,4-NADH regeneration via hydrogenated NAD+ analogs using a Pt/SiO2 catalyst with low pressure hydrogen gas.
The hydrogenation of nicotinamide analogs using a Pt/SiO2 catalyst, followed by hydride transfer to NAD+, results in the highly selective regeneration of 1,4-NADH. N-Methyl nicotinamide exhibits the highest reactivity, achieving 98% selectivity at 20 °C under 1 atm H2. This strategy provides a practical and sustainable pathway for 1,4-NADH regeneration.
期刊介绍:
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