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

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Hydroxy(tosyloxy)iodobenzene 碘代苯羟基(tosyloxy)
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-24 DOI: 10.1002/9780471264194.FOS11632.PUB5
T. Ho, Mary Fieser, L. Fieser
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引用次数: 0
(S)‐(2‐Pyrrolidinyl)Azoles
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-24 DOI: 10.1002/9780471264194.FOS11663.PUB2
T. Ho, Mary Fieser, Louis Fieser
{"title":"(S)‐(2‐Pyrrolidinyl)Azoles","authors":"T. Ho, Mary Fieser, Louis Fieser","doi":"10.1002/9780471264194.FOS11663.PUB2","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11663.PUB2","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000Michael reaction; \u0000Mannich reaction; \u0000addition; \u0000Michael reaction","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"86 1","pages":"484-485"},"PeriodicalIF":0.0,"publicationDate":"2017-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91363598","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
Mercury(II) Triflate 汞(二)Triflate
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-24 DOI: 10.1002/9780471264194.FOS11644.PUB4
T. Ho, M. Fieser, L. Fieser
{"title":"Mercury(II) Triflate","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS11644.PUB4","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11644.PUB4","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000hydration-elimination; \u0000cyclodehydation; \u0000n-tosylindolines; \u0000hydration; \u0000cyclization; \u0000pinacolatoboron B-Benzylation; \u0000MMPP; \u0000manganese(III) acetate; \u0000manganation; \u0000molybdenum-carbyne complexes","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"31 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83190321","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
Bis(Naphtho[2,1‐c])Phosphepins Bis (Naphtho[地理2 1 c]) Phosphepins
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-24 DOI: 10.1002/9780471264194.FOS11590.PUB2
T. Ho, Mary Fieser, Louis Fieser
{"title":"Bis(Naphtho[2,1‐c])Phosphepins","authors":"T. Ho, Mary Fieser, Louis Fieser","doi":"10.1002/9780471264194.FOS11590.PUB2","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11590.PUB2","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000hydrogenation; \u0000hydrogenation; \u0000addition and cycloaddition; \u0000coupling; \u00002-Benzothiazolylmethyl 2-oxoalkyl sulfones; \u0000hydroaminomethylation to alkenes; \u0000BINAMINE derivatives; \u0000BINOL-derived phosphites; \u0000cyclobutanol cleavage","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"142 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80238344","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
Bis(Naphtho[2,1‐c])Azepines
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-24 DOI: 10.1002/9780471264194.FOS11589.PUB4
T. Ho
{"title":"Bis(Naphtho[2,1‐c])Azepines","authors":"T. Ho","doi":"10.1002/9780471264194.FOS11589.PUB4","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11589.PUB4","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000aldol reaction; \u0000substitutions; \u0000addition reactions; \u0000Substitution; \u0000Aldol and Mannich Reactions; \u0000Addition and Cycloaddition; \u0000Epoxidation; \u00002-Benzothiazolylmethyl 2-oxoalkyl sulfones; \u0000hydroaminomethylation to alkenes; \u0000BINAMINE derivatives; \u0000BINOL-derived phosphites; \u0000cyclobutanol cleavage","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"131 1","pages":"000-000"},"PeriodicalIF":0.0,"publicationDate":"2017-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74273834","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
(S)-Proline Amides 脯氨酸酰胺
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-24 DOI: 10.1002/9780471264194.FOS11524.PUB4
T. Ho
{"title":"(S)-Proline Amides","authors":"T. Ho","doi":"10.1002/9780471264194.FOS11524.PUB4","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11524.PUB4","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000aldol reaction; \u0000michael reaction; \u0000allylation; \u0000kinetic resolution; \u0000aldol reaction; \u0000other condensations; \u0000epoxidation; \u0000aldol reaction; \u0000conjugate addition; \u0000addition to CN bond; \u0000palladacycles; \u0000cross-coupling reactions; \u0000Suzuki coupling; \u0000palladium(II) acetate – silver salts; \u0000palladium – aminocarbene complexes","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"122 ","pages":"000-000"},"PeriodicalIF":0.0,"publicationDate":"2017-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91466666","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
Difluoro(4‐trifluoromethylphenyl)bromane
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-24 DOI: 10.1002/9780471264194.FOS11611.PUB5
T.-L. Ho, Mary Fieser, L. Fieser
{"title":"Difluoro(4‐trifluoromethylphenyl)bromane","authors":"T.-L. Ho, Mary Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS11611.PUB5","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11611.PUB5","url":null,"abstract":"","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"98 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81136801","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
Grignard Reagents/Copper Salts 格氏试剂/铜盐
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-24 DOI: 10.1002/9780471264194.FOS11501.PUB4
T. Ho, M. Fieser, L. Fieser
{"title":"Grignard Reagents/Copper Salts","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS11501.PUB4","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11501.PUB4","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000ketone synthesis; \u0000alkylidenecyclopropanes; \u0000secondary allylic esters; \u0000addition to propargylic alcohols; \u0000conjugate addition; \u0000coupling","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"53 1","pages":"260-261"},"PeriodicalIF":0.0,"publicationDate":"2017-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86778466","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) Chloride 铁(II)氯
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-24 DOI: 10.1002/9780471264194.FOS11633.PUB2
T.-L. Ho, Mary Fieser, L. Fieser
{"title":"Iron(II) Chloride","authors":"T.-L. Ho, Mary Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS11633.PUB2","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11633.PUB2","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000redox reactions; \u0000addition to alkenes; \u0000coupling reactions; \u0000substitution reactions; \u0000organoindium reagents; \u0000N-Functionalization; \u0000indium(III) bromide; \u0000skeletal reorganization; \u0000iodosuccinimide, NIS","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"51 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88240862","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
Palladium(II) Bis(trifluoroacetate)
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-24 DOI: 10.1002/9780471264194.FOS11519.PUB4
T. Ho
{"title":"Palladium(II) Bis(trifluoroacetate)","authors":"T. Ho","doi":"10.1002/9780471264194.FOS11519.PUB4","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11519.PUB4","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000functionalization of alkenes; \u0000tetraarylallenes; \u0000wacker oxidation; \u0000cycloaddition; \u0000aroic acids; \u0000deallylation; \u0000coupling reactions; \u0000palladacycles; \u0000cross-coupling reactions; \u0000Suzuki coupling; \u0000palladium(II) acetate – silver salts; \u0000palladium – aminocarbene complexes","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"14 1","pages":"000-000"},"PeriodicalIF":0.0,"publicationDate":"2017-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76562821","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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