{"title":"封面特点:环丙化反应合成α,β-不饱和硅基酯和硅基膦酸盐的化学选择性。j . Org。化学39/2025)","authors":"Gruhapriya Jelakam, Swaraj Dey, Vikiho Wotsa, Chinnappan Sivasankar","doi":"10.1002/ejoc.70156","DOIUrl":null,"url":null,"abstract":"<p><b>The Cover Feature</b> illustrates the synthesis of α,β-unsaturated silyl esters and silyl phosphonates from α-diazo esters, and α-diazo phosphonate esters with allyl trimethyl silane in the presence of a catalyst. The sun symbolizes the catalyst, [Ru(Cp)*Cl<sub>2</sub>]<sub>n</sub>, which activates the trees and the canal through which acetonitrile and allyl trimethyl silane flow. These substances are absorbed by the trees next to the canal, along with fertilizer (diazo), to produce as fruits α,β-unsaturated silyl esters at 0 °C (right) and α,β-unsaturated silyl phosphonates at 50 °C (left). More information can be found in the Research Article by C. Sivasankar and co-workers (DOI: 10.1002/ejoc.202500133).\n <figure>\n <div><picture>\n <source></source></picture><p></p>\n </div>\n </figure></p>","PeriodicalId":167,"journal":{"name":"European Journal of Organic Chemistry","volume":"28 39","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://chemistry-europe.onlinelibrary.wiley.com/doi/epdf/10.1002/ejoc.70156","citationCount":"0","resultStr":"{\"title\":\"Cover Feature: Chemoselective Synthesis of α,β-Unsaturated Silyl Esters and Silyl Phosphonates over Cyclopropanation (Eur. J. Org. Chem. 39/2025)\",\"authors\":\"Gruhapriya Jelakam, Swaraj Dey, Vikiho Wotsa, Chinnappan Sivasankar\",\"doi\":\"10.1002/ejoc.70156\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><b>The Cover Feature</b> illustrates the synthesis of α,β-unsaturated silyl esters and silyl phosphonates from α-diazo esters, and α-diazo phosphonate esters with allyl trimethyl silane in the presence of a catalyst. The sun symbolizes the catalyst, [Ru(Cp)*Cl<sub>2</sub>]<sub>n</sub>, which activates the trees and the canal through which acetonitrile and allyl trimethyl silane flow. These substances are absorbed by the trees next to the canal, along with fertilizer (diazo), to produce as fruits α,β-unsaturated silyl esters at 0 °C (right) and α,β-unsaturated silyl phosphonates at 50 °C (left). More information can be found in the Research Article by C. Sivasankar and co-workers (DOI: 10.1002/ejoc.202500133).\\n <figure>\\n <div><picture>\\n <source></source></picture><p></p>\\n </div>\\n </figure></p>\",\"PeriodicalId\":167,\"journal\":{\"name\":\"European Journal of Organic Chemistry\",\"volume\":\"28 39\",\"pages\":\"\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-10-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://chemistry-europe.onlinelibrary.wiley.com/doi/epdf/10.1002/ejoc.70156\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"European Journal of Organic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejoc.70156\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Organic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejoc.70156","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Cover Feature: Chemoselective Synthesis of α,β-Unsaturated Silyl Esters and Silyl Phosphonates over Cyclopropanation (Eur. J. Org. Chem. 39/2025)
The Cover Feature illustrates the synthesis of α,β-unsaturated silyl esters and silyl phosphonates from α-diazo esters, and α-diazo phosphonate esters with allyl trimethyl silane in the presence of a catalyst. The sun symbolizes the catalyst, [Ru(Cp)*Cl2]n, which activates the trees and the canal through which acetonitrile and allyl trimethyl silane flow. These substances are absorbed by the trees next to the canal, along with fertilizer (diazo), to produce as fruits α,β-unsaturated silyl esters at 0 °C (right) and α,β-unsaturated silyl phosphonates at 50 °C (left). More information can be found in the Research Article by C. Sivasankar and co-workers (DOI: 10.1002/ejoc.202500133).
期刊介绍:
The European Journal of Organic Chemistry (2019 ISI Impact Factor 2.889) publishes Full Papers, Communications, and Minireviews from the entire spectrum of synthetic organic, bioorganic and physical-organic chemistry. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies.
The following journals have been merged to form two leading journals, the European Journal of Organic Chemistry and the European Journal of Inorganic Chemistry:
Liebigs Annalen
Bulletin des Sociétés Chimiques Belges
Bulletin de la Société Chimique de France
Gazzetta Chimica Italiana
Recueil des Travaux Chimiques des Pays-Bas
Anales de Química
Chimika Chronika
Revista Portuguesa de Química
ACH—Models in Chemistry
Polish Journal of Chemistry.