Correction to “Ring Opening of Aziridines by Pendant Silanols Allows for Preparations of (±)-Clavaminol H, (±)-Des-Acetyl-Clavaminol H, (±)-Dihydrosphingosine, and (±)-N-Hexanoyldihydrosphingosine”

IF 4.9 1区化学 Q1 CHEMISTRY, ORGANIC

Organic Letters Pub Date : 2025-04-01 DOI:10.1021/acs.orglett.5c01213

Someshwar Nagamalla, Debobrata Paul, Joel T. Mague, Shyam Sathyamoorthi

{"title":"Correction to “Ring Opening of Aziridines by Pendant Silanols Allows for Preparations of (±)-Clavaminol H, (±)-Des-Acetyl-Clavaminol H, (±)-Dihydrosphingosine, and (±)-N-Hexanoyldihydrosphingosine”","authors":"Someshwar Nagamalla, Debobrata Paul, Joel T. Mague, Shyam Sathyamoorthi","doi":"10.1021/acs.orglett.5c01213","DOIUrl":null,"url":null,"abstract":"We have corrected the synthetic procedures for N–H aziridines in the Supporting Information. In the original version, Rh2(esp)2 was accidentally omitted from the synthetic procedures. The Supporting Information is available free of charge at https://pubs.acs.org/doi/10.1021/acs.orglett.5c01213. Experimental procedures, reasoning for structural assignments, NMR spectra, and crystallographic information (PDF) Correction to\n“Ring Opening of Aziridines by\nPendant Silanols Allows for Preparations of (±)-Clavaminol H,\n(±)-Des-Acetyl-Clavaminol H, (±)-Dihydrosphingosine, and\n(±)-N-Hexanoyldihydrosphingosine” 0 views 0 shares 0 downloads Most electronic Supporting Information files are available without a subscription to ACS Web Editions. Such files may be downloaded by article for research use (if there is a public use license linked to the relevant article, that license may permit other uses). Permission may be obtained from ACS for other uses through requests via the RightsLink permission system: http://pubs.acs.org/page/copyright/permissions.html. This article has not yet been cited by other publications.","PeriodicalId":54,"journal":{"name":"Organic Letters","volume":"721 1","pages":""},"PeriodicalIF":4.9000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic Letters","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.orglett.5c01213","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}

引用次数: 0

Abstract

We have corrected the synthetic procedures for N–H aziridines in the Supporting Information. In the original version, Rh₂(esp)₂ was accidentally omitted from the synthetic procedures. The Supporting Information is available free of charge at https://pubs.acs.org/doi/10.1021/acs.orglett.5c01213. Experimental procedures, reasoning for structural assignments, NMR spectra, and crystallographic information (PDF) Correction to “Ring Opening of Aziridines by Pendant Silanols Allows for Preparations of (±)-Clavaminol H, (±)-Des-Acetyl-Clavaminol H, (±)-Dihydrosphingosine, and (±)-N-Hexanoyldihydrosphingosine” 0 views 0 shares 0 downloads Most electronic Supporting Information files are available without a subscription to ACS Web Editions. Such files may be downloaded by article for research use (if there is a public use license linked to the relevant article, that license may permit other uses). Permission may be obtained from ACS for other uses through requests via the RightsLink permission system: http://pubs.acs.org/page/copyright/permissions.html. This article has not yet been cited by other publications.

查看原文本刊更多论文

对 "通过硅烷偶联醇打开氮丙啶环，制备出(±)-克拉维诺 H、(±)-去乙酰基克拉维诺 H、(±)-二氢鞘磷脂和(±)-N-己酰基二氢鞘磷脂 "的更正

本文章由计算机程序翻译，如有差异，请以英文原文为准。

求助全文

约1分钟内获得全文求助全文

来源期刊

Organic Letters 化学-有机化学

CiteScore

9.30

自引率

11.50%

发文量

1607

审稿时长

1.5 months

期刊介绍： Organic Letters invites original reports of fundamental research in all branches of the theory and practice of organic, physical organic, organometallic,medicinal, and bioorganic chemistry. Organic Letters provides rapid disclosure of the key elements of significant studies that are of interest to a large portion of the organic community. In selecting manuscripts for publication, the Editors place emphasis on the originality, quality and wide interest of the work. Authors should provide enough background information to place the new disclosure in context and to justify the rapid publication format. Back-to-back Letters will be considered. Full details should be reserved for an Article, which should appear in due course.