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Fieser and Fieser's Reagents for Organic Synthesis最新文献

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Acetylacetonato(Dicarbonyl)Rhodium(I) Acetylacetonato(二羰基铑)(我)
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11688.PUB6
T. Ho
{"title":"Acetylacetonato(Dicarbonyl)Rhodium(I)","authors":"T. Ho","doi":"10.1002/9780471264194.FOS11688.PUB6","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11688.PUB6","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000arylation of aldehydes; \u0000Michael addition; \u0000chain elongation; \u0000chain elongation; \u0000hydroformylation; \u0000hydroformylation; \u0000silylative cyclization; \u00004-alkynones; \u0000hydroformylation; \u0000β-chloro enones; \u0000alkynylation; \u0000alkynylation; \u0000coupling; \u0000addition to α-dicarbonyl compounds; \u0000reduction; \u0000hydroformylation; \u0000acetylacetonato(dicarbonyl)rhodium(I); \u0000acetylacetonato(1,5-cyclooctadiene)rhodium(I); \u0000hydroformylation; \u0000hydroarylation; \u0000allyltrichlorosilanes; \u0000Stetter and Michael reactions","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83305827","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Tin (II) Chloride 氯化锡(II
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11786.PUB2
T. Ho, Mary Fieser, L. Fieser
{"title":"Tin (II) Chloride","authors":"T. Ho, Mary Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS11786.PUB2","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11786.PUB2","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000decupration; \u0000hydroxyallylation; \u0000tetrabutylammonium fluoride, TBAF; \u0000tetrabutylammonium difluorotriphenylsilicate; \u0000tetracarbonylhydridorhenium; \u0000titanocene bis(triethyl phosphite); \u0000trimethylsilyl trifluoromethanesulfonate","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89386655","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Iron(III) Triflate 铁(III) Triflate
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11750.PUB2
T. Ho, M. Fieser, L. Fieser
{"title":"Iron(III) Triflate","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS11750.PUB2","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11750.PUB2","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000addition; \u0000benzylation; \u0000organoindium reagents; \u0000N-Functionalization; \u0000indium(III) bromide; \u0000skeletal reorganization; \u0000iodosuccinimide, NIS","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89397836","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Tin(IV) chloride 氯化锡(IV)
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11437.PUB3
T. Ho, M. Fieser, L. Fieser
{"title":"Tin(IV) chloride","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS11437.PUB3","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11437.PUB3","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000N-alkylation; \u0000allylation; \u0000Diels-Alder reaction and Schmidt reaction; \u0000haloamidation; \u0000n-nitrosation; \u0000substitution reaction; \u0000peroxy compounds; \u0000tetrahydrofurans from cyclopropanes; \u0000rearrangement; \u0000alkyl lactates; \u0000claisen rearrangement; \u0000fragmentative defunctionalization; \u0000hetero-diels–alder reaction; \u0000aromatization; \u0000cyclization; \u0000Sn-W mixed hydroxide; \u0000substitution; \u0000annulation","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76162893","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Rhodium(II) carboxamidates (2) carboxamidates铑
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS08767.PUB4
T. Ho, M. Fieser, L. Fieser
{"title":"Rhodium(II) carboxamidates","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS08767.PUB4","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS08767.PUB4","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000three-membered rings; \u0000five-membered rings; \u0000C-H insertion; \u0000rearrangement; \u00001-acetoxyazulenes; \u0000coupling; \u0000Hetero Diels-Alder Reaction; \u0000Recoverable Specimens; \u0000Cycloadditions; \u0000Oxidations; \u0000Cyclization; \u0000cycloadditions; \u0000oxidation","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76050885","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Iron(II) oxalate 草酸铁(II)
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11865.PUB2
T. Ho
{"title":"Iron(II) oxalate","authors":"T. Ho","doi":"10.1002/9780471264194.FOS11865.PUB2","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11865.PUB2","url":null,"abstract":"","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77358393","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Lead(IV) Acetate 醋酸铅(IV)
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11424
T. Ho, M. Fieser, L. Fieser
{"title":"Lead(IV) Acetate","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS11424","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11424","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000oxidation; \u0000decarboxylation; \u0000oxidative degradation; \u0000cyclization; \u0000halogenation; \u00002-aroylaraldehydes; \u0000lanthanum chloride; \u0000lanthanum isopropoxide; \u0000alkyne hydroalkoxylation; \u0000aziridine reductive cleavage; \u0000Darzens reaction","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74790238","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Gallium(III) Chloride 氯化镓(III)
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS05389.PUB3
Tse‐Lok Ho, M. Fieser, L. Fieser
{"title":"Gallium(III) Chloride","authors":"Tse‐Lok Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS05389.PUB3","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS05389.PUB3","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000diels—alder reaction; \u0000gallium(III) chloride; \u0000Friedel-Crafts reaction; \u0000Sonogashira coupling; \u0000Grignard reagents/cobalt(II) salts; \u0000Gold(III) chloride – silver salts","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87747497","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Iron(III) bromide 溴化铁(III)
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11863
T. Ho, M. Fieser, L. Fieser
{"title":"Iron(III) bromide","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS11863","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11863","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000organoindium reagents; \u0000N-Functionalization; \u0000indium(III) bromide; \u0000skeletal reorganization; \u0000iodosuccinimide, NIS","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83485334","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Ytterbium(III) triflate
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11231.PUB2
T. Ho, M. Fieser, L. Fieser
{"title":"Ytterbium(III) triflate","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS11231.PUB2","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11231.PUB2","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000conjugate addition; \u0000cross-aldol reactions; \u0000allylation of aldehydes; \u0000isomerization of silyl ketene acetals; \u0000Friedel–Crafts acylation; \u0000cleavage of small heterocycles; \u0000glycosylation; \u0000hydroxyl derivatization; \u0000substitutions; \u0000heterocycles; \u00001-arenylalkenes; \u0000condensations; \u0000enolization; \u0000elimination; \u0000carbonyl-ene cyclization; \u0000ring expansion; \u0000pyridines; \u0000benzyl ethers; \u0000mandelic acids; \u0000condensations; \u0000allylation; \u0000heterocycles; \u0000hydroalkoxylation; \u0000diallylation; \u0000substitution; \u0000guanidines; \u0000Friedel–Crafts Reaction; \u0000cycloaddition; \u0000Ytterbium(III) isopropoxide; \u0000Ytterbium(III) triflate; \u0000Yb(OTf)3 allenylaminophosphates; \u0000cinnamaldehyde; \u0000heterocycle synthesis","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81046684","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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