勘误：1- oxa -2,6-重氮杂环[3.3]-庚烷作为一种新的潜在哌嗪类生物异构体-氮杂环[1.1.0]丁烷的流动辅助制备和衍生化

IF 4.4 2区化学 Q2 CHEMISTRY, APPLIED Advanced Synthesis & Catalysis Pub Date : 2024-12-30 DOI:10.1002/adsc.202401389

{"title":"勘误：1- oxa -2,6-重氮杂环[3.3]-庚烷作为一种新的潜在哌嗪类生物异构体-氮杂环[1.1.0]丁烷的流动辅助制备和衍生化","authors":"","doi":"10.1002/adsc.202401389","DOIUrl":null,"url":null,"abstract":"<p>In the research article by Elena Graziano, Philipp Natho, Michael Andresini, Fabrizio Mastrolorito, Iktedar Mahdi, Ernesto Mesto, Marco Colella, Leonardo Degennaro, Orazio Nicolotti, and Renzo Luisi, in Issue 18, 2024, pp. 3894–3902 (DOI: 10.1002/adsc.202400781), the acknowledgement section should have included mention of additional financial support. R.L., L.D., M.A. acknowledge financial support from the European Commission – Horizon Europe Framework, project SusPharma grant agreement No 101057430. I.M. acknowledges funding from the European Commission′s Horizon Europe research and innovation programme through the Marie Skłodowska-Curie doctoral network “GreenDigiPharma” (grant agreement No 101073089). The authors apologize for this oversight</p>","PeriodicalId":118,"journal":{"name":"Advanced Synthesis & Catalysis","volume":"81 1","pages":""},"PeriodicalIF":4.4000,"publicationDate":"2024-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"CORRIGENDUM: 1-Oxa-2,6-Diazaspiro[3.3]-heptane as a New Potential Piperazine Bioisostere – Flow-Assisted Preparation and Derivatisation by Strain-Release of Azabicyclo[1.1.0]butanes\",\"authors\":\"\",\"doi\":\"10.1002/adsc.202401389\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>In the research article by Elena Graziano, Philipp Natho, Michael Andresini, Fabrizio Mastrolorito, Iktedar Mahdi, Ernesto Mesto, Marco Colella, Leonardo Degennaro, Orazio Nicolotti, and Renzo Luisi, in Issue 18, 2024, pp. 3894–3902 (DOI: 10.1002/adsc.202400781), the acknowledgement section should have included mention of additional financial support. R.L., L.D., M.A. acknowledge financial support from the European Commission – Horizon Europe Framework, project SusPharma grant agreement No 101057430. I.M. acknowledges funding from the European Commission′s Horizon Europe research and innovation programme through the Marie Skłodowska-Curie doctoral network “GreenDigiPharma” (grant agreement No 101073089). The authors apologize for this oversight</p>\",\"PeriodicalId\":118,\"journal\":{\"name\":\"Advanced Synthesis & Catalysis\",\"volume\":\"81 1\",\"pages\":\"\"},\"PeriodicalIF\":4.4000,\"publicationDate\":\"2024-12-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Synthesis & Catalysis\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1002/adsc.202401389\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Synthesis & Catalysis","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/adsc.202401389","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}

引用次数: 0

摘要

在Elena Graziano， Philipp Natho, Michael Andresini, Fabrizio Mastrolorito, Iktedar Mahdi, Ernesto Mesto, Marco Colella, Leonardo Degennaro， Orazio Nicolotti和Renzo Luisi的研究文章中，在第18期，2024，第3894-3902页（DOI: 10.1002/ adc .202400781），致谢部分应该包括提到额外的财政支持。r.l.， L.D， M.A.承认欧盟委员会-地平线欧洲框架的财政支持，项目SusPharma资助协议号101057430。imm通过Marie Skłodowska-Curie博士网络“GreenDigiPharma”（资助协议号101073089）承认欧盟委员会的“地平线欧洲”研究和创新计划的资助。作者为这个疏忽道歉

本文章由计算机程序翻译，如有差异，请以英文原文为准。

查看原文

微信好友朋友圈 QQ好友复制链接

本刊更多论文

CORRIGENDUM: 1-Oxa-2,6-Diazaspiro[3.3]-heptane as a New Potential Piperazine Bioisostere – Flow-Assisted Preparation and Derivatisation by Strain-Release of Azabicyclo[1.1.0]butanes

In the research article by Elena Graziano, Philipp Natho, Michael Andresini, Fabrizio Mastrolorito, Iktedar Mahdi, Ernesto Mesto, Marco Colella, Leonardo Degennaro, Orazio Nicolotti, and Renzo Luisi, in Issue 18, 2024, pp. 3894–3902 (DOI: 10.1002/adsc.202400781), the acknowledgement section should have included mention of additional financial support. R.L., L.D., M.A. acknowledge financial support from the European Commission – Horizon Europe Framework, project SusPharma grant agreement No 101057430. I.M. acknowledges funding from the European Commission′s Horizon Europe research and innovation programme through the Marie Skłodowska-Curie doctoral network “GreenDigiPharma” (grant agreement No 101073089). The authors apologize for this oversight

求助全文

通过发布文献求助，成功后即可免费获取论文全文。去求助

来源期刊

Advanced Synthesis & Catalysis 化学-应用化学

CiteScore

9.40

自引率

7.40%

发文量

447

审稿时长

1.8 months

期刊介绍： Advanced Synthesis & Catalysis (ASC) is the leading primary journal in organic, organometallic, and applied chemistry. The high impact of ASC can be attributed to the unique focus of the journal, which publishes exciting new results from academic and industrial labs on efficient, practical, and environmentally friendly organic synthesis. While homogeneous, heterogeneous, organic, and enzyme catalysis are key technologies to achieve green synthesis, significant contributions to the same goal by synthesis design, reaction techniques, flow chemistry, and continuous processing, multiphase catalysis, green solvents, catalyst immobilization, and recycling, separation science, and process development are also featured in ASC. The Aims and Scope can be found in the Notice to Authors or on the first page of the table of contents in every issue.