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

{"title":"Platinum(II) iodide","authors":"T. Ho","doi":"10.1002/9780471264194.FOS11894.PUB2","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11894.PUB2","url":null,"abstract":"","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"126 1","pages":"396-396"},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86584150","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}

{"title":"Gold - carbene complexes","authors":"T. Ho","doi":"10.1002/9780471264194.FOS11854.PUB2","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11854.PUB2","url":null,"abstract":"","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"56 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80215984","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}

{"title":"Phenyliodine(III) triflate","authors":"T.-L. Ho, Mary Fieser, Louis Fieser","doi":"10.1002/9780471264194.FOS11889","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11889","url":null,"abstract":"","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"47 1","pages":"390-391"},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80980467","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}

{"title":"Bis[(1,5‐cyclooctadiene)hydroxyiridium]","authors":"T. Ho, Mary Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS11708","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11708","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000annulation; \u0000redox condensation; \u0000coupling reactions","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"83 5 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89597121","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}

{"title":"Rhodium(II) acetate","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS08761.PUB2","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS08761.PUB2","url":null,"abstract":"","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"110 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90707486","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}

{"title":"2,2,2-Trifluorodiazoethane","authors":"T. Ho, Mary Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS10407","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS10407","url":null,"abstract":"","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"17 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91061070","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}

{"title":"Manganese(II) Triflate","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS11643","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11643","url":null,"abstract":"","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"141-142 1","pages":"000-000"},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79149950","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}

{"title":"Chlorotris(triphenylphosphine)rhodium(I)","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS11484.PUB3","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11484.PUB3","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000homogeneous catalytic hydrogenation; \u0000deformylation; \u0000decarbonylation; \u0000angular methylation; \u0000other reactions; \u0000homogeneous hydrogenation catalyst; \u0000valence tautomerization; \u0000cyclooligomerization of allene; \u0000synthesis of nitriles from secondary amides; \u0000selective acetalation; \u0000decarbonylation; \u0000deuteration of olefins; \u0000decarbonylation; \u0000desulfonylation; \u0000cyclization; \u0000fluorenone from benzoic anhydride; \u0000homogeneous catalytic hydrogenation of unhindered double bonds; \u0000selective hydrogenation of prostaglandins; \u0000hydrogenation of allenes; \u0000reduction of alkenes and alkynes; \u0000reduction of diazonium fluoroborates; \u0000alcoholysis of diarylsilanes; \u0000cleavage of allyl ethers; \u0000α-spinasterol; \u0000decomposition of peroxides; \u0000synthesis of quinones; \u0000diyne reaction; \u0000polysubstituted naphthalenes; \u0000conjugated diynes; \u0000reduction of schiff bases; \u0000silyl thioethers; \u0000synthesis of nitriles from secondary amides; \u0000review; \u0000homogeneous hydrogenation catalysts; \u0000aldehyde decarbonylation; \u0000dimerization of α-hydroxy acetylenes; \u0000stereoselective hydrogenation; \u0000catalytic hydroacylation; \u0000cyclopentanones; \u0000protection of primary amines; \u0000[2 + 2 + 2]cycloadditions; \u00003,4-disubstituted cyclopentanones; \u0000decarbonylation of sugars; \u0000hydroboration of alkenes; \u0000cyclization of 1,6-enynes; \u0000hydroboration of alkenes; \u0000decarbonylation of aldoses; \u0000diels–alder catalysis; \u0000cyclization of triynes to benzenes; \u0000isomerization of allyl ethers; \u0000hydroboration; \u0000alkenylsilanes; \u0000homologous pericyclic reactions; \u0000cycloisomerizations; \u0000c-aryl spiroglycosides; \u0000allylic alkylations; \u0000hydroacylation; \u0000hydrosilylations; \u0000cycloalkenes; \u0000allylic alkylations; \u0000reformatsky-type reaction; \u0000cycloadditions; \u0000addition to vinyl aminopropyl ethers; \u0000hydroboration, hydrosilylation and hydrophosphonylation; \u0000reduction; \u0000alkenylation; \u0000isomerization; \u0000o-alkylation; \u0000cycloadditions; \u0000reformatsky-type reaction; \u0000enone-alkene union; \u0000isomerization; \u0000allylation; \u0000reductive trifluoromethylation; \u0000o-alkylation; \u0000methylenation; \u0000trifluoromethylation; \u0000reformatsky reaction; \u0000reductive acylation; \u0000reductive silylation; \u0000cycloaddition; \u0000rearrangement; \u0000substitution; \u0000hydration; \u0000methylenation; \u0000coupling reactions; \u0000addition reactions; \u0000cycloaddition","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"34 1","pages":"000-000"},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76785251","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}

{"title":"2,2,6,6-Tetramethylpiperidinylzinc chloride","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS11927","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11927","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \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":"16 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74646962","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}

{"title":"Gold(I) Chloride","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS11499.PUB5","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11499.PUB5","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000oxidation; \u0000cyclization and cycloaddition; \u0000O-silylation; \u0000spiroacetals; \u0000isomerization; \u0000cycloelimination; \u0000substitution; \u0000addition; \u0000cycloisomerization; \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":"61 1","pages":"000-000"},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87395334","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}