{"title":"Hydroxy(tosyloxy)iodobenzene","authors":"T. Ho, Mary Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS11632.PUB5","DOIUrl":null,"url":null,"abstract":"This article has no abstract. \n \nKeywords: \n \nflavanones Isoflavones; \nreview; \n1,3-Enynes; \nα-tosyloxylation of ketones; \noxidation of chromanones; \nallylic oxidation; \nC-tosyloxylation; \nstille coupling; \nring expansion; \nsulfoxides; \n4-alkoxy-2-arylquinolines; \ncleavage of N′,N′-dialkylhydrazides; \nalkynyl tosylates; \noxidation; \ncyclization; \npreparation; \nbenzyl ketones; \nbiaryls; \ncoupling; \nhafnium triflate; \nWolff-Kishner reduction; \nBaeyer-Villiger oxidation; \nhydrogen peroxide - metal catalysts; \npropargyl alcohol functionalization","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"14 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2017-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fieser and Fieser's Reagents for Organic Synthesis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/9780471264194.FOS11632.PUB5","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
碘代苯羟基(tosyloxy)
这篇文章没有摘要。关键词:黄酮;异黄酮;审查;1、3-Enynes;酮类α-甲氧基化;氧化激素;烯丙基的氧化;C-tosyloxylation;stille耦合;环扩张;亚砜;4-alkoxy-2-arylquinolines;N '，N ' -二烷基肼的裂解作用;炔基甲苯磺酸盐;氧化;环化;准备;苄基酮;biaryls;耦合;铪triflate;Wolff-Kishner减少;Baeyer-Villiger氧化;过氧化氢-金属催化剂;丙炔醇功能化
本文章由计算机程序翻译，如有差异，请以英文原文为准。
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