{"title":"Chlorotris(三苯基膦)铑(我)","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":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"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\":null,\"pages\":null},\"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}","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