{"title":"用于Wittig反应的二氧化硅负载活性Ni纳米催化剂","authors":"V. Srivastava","doi":"10.2174/1570178620666230821143013","DOIUrl":null,"url":null,"abstract":"\n\nThe preparation and characterization of SBA-15 supported Ni catalysts with varying metal loading (1, 2, and 3% by weight) was carried out using the impregnation technique, followed by a rigorous characterization using advanced analytical techniques. The catalytic performance of the synthesized catalysts was evaluated for the Wittig-type olefination reaction, and it was found that the SBA-15-3Ni catalyst exhibited superior activity for this reaction under mild reaction conditions (70 °C and 1 hour). The corresponding stilbenes were obtained in good yield, although with low to average diastereoselectivity. An important feature of this protocol is that the proposed methodology is especially efficient for the synthesis of stilbenes since no additives are required to serve as a hydrogen acceptor. Moreover, the new catalytic system was successfully employed for the synthesis of polymethoxylated and polyhydroxylated stilbenes, including resveratrol and DMU-212, with high yield and easy product isolation. A key advantage of this protocol is that the catalysts can be reused for up to 5 runs without significant loss in catalytic activity, which makes this approach highly sustainable and cost-effective. Additionally, the ligand-free approach proposed in this study is an added advantage, which makes it more attractive for large-scale synthesis of biologically active compounds.\n","PeriodicalId":18116,"journal":{"name":"Letters in Organic Chemistry","volume":" ","pages":""},"PeriodicalIF":0.7000,"publicationDate":"2023-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Silica-supported active Ni Nanocatalyst for Wittig Reaction\",\"authors\":\"V. Srivastava\",\"doi\":\"10.2174/1570178620666230821143013\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n\\nThe preparation and characterization of SBA-15 supported Ni catalysts with varying metal loading (1, 2, and 3% by weight) was carried out using the impregnation technique, followed by a rigorous characterization using advanced analytical techniques. The catalytic performance of the synthesized catalysts was evaluated for the Wittig-type olefination reaction, and it was found that the SBA-15-3Ni catalyst exhibited superior activity for this reaction under mild reaction conditions (70 °C and 1 hour). The corresponding stilbenes were obtained in good yield, although with low to average diastereoselectivity. An important feature of this protocol is that the proposed methodology is especially efficient for the synthesis of stilbenes since no additives are required to serve as a hydrogen acceptor. Moreover, the new catalytic system was successfully employed for the synthesis of polymethoxylated and polyhydroxylated stilbenes, including resveratrol and DMU-212, with high yield and easy product isolation. A key advantage of this protocol is that the catalysts can be reused for up to 5 runs without significant loss in catalytic activity, which makes this approach highly sustainable and cost-effective. Additionally, the ligand-free approach proposed in this study is an added advantage, which makes it more attractive for large-scale synthesis of biologically active compounds.\\n\",\"PeriodicalId\":18116,\"journal\":{\"name\":\"Letters in Organic Chemistry\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.7000,\"publicationDate\":\"2023-08-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Letters in Organic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.2174/1570178620666230821143013\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Letters in Organic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.2174/1570178620666230821143013","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Silica-supported active Ni Nanocatalyst for Wittig Reaction
The preparation and characterization of SBA-15 supported Ni catalysts with varying metal loading (1, 2, and 3% by weight) was carried out using the impregnation technique, followed by a rigorous characterization using advanced analytical techniques. The catalytic performance of the synthesized catalysts was evaluated for the Wittig-type olefination reaction, and it was found that the SBA-15-3Ni catalyst exhibited superior activity for this reaction under mild reaction conditions (70 °C and 1 hour). The corresponding stilbenes were obtained in good yield, although with low to average diastereoselectivity. An important feature of this protocol is that the proposed methodology is especially efficient for the synthesis of stilbenes since no additives are required to serve as a hydrogen acceptor. Moreover, the new catalytic system was successfully employed for the synthesis of polymethoxylated and polyhydroxylated stilbenes, including resveratrol and DMU-212, with high yield and easy product isolation. A key advantage of this protocol is that the catalysts can be reused for up to 5 runs without significant loss in catalytic activity, which makes this approach highly sustainable and cost-effective. Additionally, the ligand-free approach proposed in this study is an added advantage, which makes it more attractive for large-scale synthesis of biologically active compounds.
期刊介绍:
Aims & Scope
Letters in Organic Chemistry publishes original letters (short articles), research articles, mini-reviews and thematic issues based on mini-reviews and short articles, in all areas of organic chemistry including synthesis, bioorganic, medicinal, natural products, organometallic, supramolecular, molecular recognition and physical organic chemistry. The emphasis is to publish quality papers rapidly by taking full advantage of latest technology for both submission and review of the manuscripts.
The journal is an essential reading for all organic chemists belonging to both academia and industry.