{"title":"Chlorotris(triphenylphosphine)rhodium(I)","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS11484.PUB3","DOIUrl":null,"url":null,"abstract":"This article has no abstract. \n \nKeywords: \n \nhomogeneous catalytic hydrogenation; \ndeformylation; \ndecarbonylation; \nangular methylation; \nother reactions; \nhomogeneous hydrogenation catalyst; \nvalence tautomerization; \ncyclooligomerization of allene; \nsynthesis of nitriles from secondary amides; \nselective acetalation; \ndecarbonylation; \ndeuteration of olefins; \ndecarbonylation; \ndesulfonylation; \ncyclization; \nfluorenone from benzoic anhydride; \nhomogeneous catalytic hydrogenation of unhindered double bonds; \nselective hydrogenation of prostaglandins; \nhydrogenation of allenes; \nreduction of alkenes and alkynes; \nreduction of diazonium fluoroborates; \nalcoholysis of diarylsilanes; \ncleavage of allyl ethers; \nα-spinasterol; \ndecomposition of peroxides; \nsynthesis of quinones; \ndiyne reaction; \npolysubstituted naphthalenes; \nconjugated diynes; \nreduction of schiff bases; \nsilyl thioethers; \nsynthesis of nitriles from secondary amides; \nreview; \nhomogeneous hydrogenation catalysts; \naldehyde decarbonylation; \ndimerization of α-hydroxy acetylenes; \nstereoselective hydrogenation; \ncatalytic hydroacylation; \ncyclopentanones; \nprotection of primary amines; \n[2 + 2 + 2]cycloadditions; \n3,4-disubstituted cyclopentanones; \ndecarbonylation of sugars; \nhydroboration of alkenes; \ncyclization of 1,6-enynes; \nhydroboration of alkenes; \ndecarbonylation of aldoses; \ndiels–alder catalysis; \ncyclization of triynes to benzenes; \nisomerization of allyl ethers; \nhydroboration; \nalkenylsilanes; \nhomologous pericyclic reactions; \ncycloisomerizations; \nc-aryl spiroglycosides; \nallylic alkylations; \nhydroacylation; \nhydrosilylations; \ncycloalkenes; \nallylic alkylations; \nreformatsky-type reaction; \ncycloadditions; \naddition to vinyl aminopropyl ethers; \nhydroboration, hydrosilylation and hydrophosphonylation; \nreduction; \nalkenylation; \nisomerization; \no-alkylation; \ncycloadditions; \nreformatsky-type reaction; \nenone-alkene union; \nisomerization; \nallylation; \nreductive trifluoromethylation; \no-alkylation; \nmethylenation; \ntrifluoromethylation; \nreformatsky reaction; \nreductive acylation; \nreductive silylation; \ncycloaddition; \nrearrangement; \nsubstitution; \nhydration; \nmethylenation; \ncoupling reactions; \naddition reactions; \ncycloaddition","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"34 1","pages":"000-000"},"PeriodicalIF":0.0000,"publicationDate":"2017-02-21","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.FOS11484.PUB3","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Chlorotris(三苯基膦)铑(我)
这篇文章没有摘要。关键词:均相催化加氢;deformylation;脱羰作用;角甲基化;其他反应;均相加氢催化剂;价互变异构化;烯环寡聚;仲酰胺合成腈的研究选择性缩醛;脱羰作用;烯烃的氘化;脱羰作用;desulfonylation;环化;苯甲酸酐合成芴酮;无阻碍双键均相催化加氢反应;前列腺素选择性加氢;烯的加氢;烯烃和炔烃的还原;还原氟硼酸重氮;二芳基硅烷醇解;烯丙基醚的裂解;α-spinasterol;过氧化物的分解;醌类化合物的合成;diyne反应;为萘;共轭diynes;席夫碱还原;甲硅烷基硫醚;仲酰胺合成腈的研究审查;均相加氢催化剂;醛脱羰作用;α-羟基乙炔的二聚化反应立体选择加氢;催化hydroacylation;环戊酮;伯胺保护;[2 + 2 + 2]环加法;3, 4-disubstituted环戊酮;糖的脱碳;烯烃的硼化;1,6-炔的环化;烯烃的硼化;醛糖的脱碳;diels-alder催化;三炔合成苯的环化反应;烯丙基醚异构化;硼氢化反应;alkenylsilanes;同源周环反应;cycloisomerizations;c-aryl spiroglycosides;烯丙基的烷基化;hydroacylation;氢化硅烷化;环烯;烯丙基的烷基化;reformatsky-type反应;环加;乙烯基氨基丙醚的加成;硼氢化、硅氢化和氢膦化;减少;alkenylation;异构化;o-alkylation;环加;reformatsky-type反应;enone-alkene联盟;异构化;烯丙基化;还原trifluoromethylation;o-alkylation;methylenation;trifluoromethylation;reformatsky反应;还原酰化;还原甲硅烷基化;环加成作用;重排;替换;水化;methylenation;耦合反应;加成反应;环加成作用
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