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

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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":"40 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":"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
1,1,3,3‐Tetrakis(trifluoromethanesulfonyl)propane 1, 1, 3, 3 Tetrakis应承担(trifluoromethanesulfonyl)丙烷
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11926.PUB2
T. Ho
{"title":"1,1,3,3‐Tetrakis(trifluoromethanesulfonyl)propane","authors":"T. Ho","doi":"10.1002/9780471264194.FOS11926.PUB2","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11926.PUB2","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":"59 11 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87049314","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":"44 1","pages":""},"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
Palladium(II) acetate 醋酸钯(II)
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS07552.PUB6
T. Ho, M. Fieser, R. Danheiser, W. Roush, L. Fieser
{"title":"Palladium(II) acetate","authors":"T. Ho, M. Fieser, R. Danheiser, W. Roush, L. Fieser","doi":"10.1002/9780471264194.FOS07552.PUB6","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS07552.PUB6","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000oxidative dimerization of β-substituted α-olefins; \u0000benzylic oxidation of toluenes; \u0000π-allylpalladium complexes; \u0000cyclopropanation; \u0000substitution of vinylic hydrogens; \u0000oxidation of ethylene; \u0000cyclopropanation; \u0000examples; \u0000ArI  Ar–Ar; \u0000acetoxylation of arenes; \u0000arylation of allylic alcohols with aryl halides; \u0000α,β-enones; \u00001,4-dienes; \u0000(E)- and (Z)-alkenes; \u0000arylation of allylic alcohols; \u0000arylation of olefins; \u0000terminal 1,3-dienes; \u00002,2,7,7,12,13,17,18-octamethylisobacteriochlorin; \u0000α,β-enones; \u0000benzohydrofuranes; \u0000transannular reactions of grayanotoxin-II; \u0000cyclopentenes; \u00003-methyl-2-cyclopentenones; \u0000polycyclic indoles; \u0000β-lactams; \u0000intramolecular cyclization via π-allylpalladium complexes; \u0000β-aryl-α,β-unsaturated carbonyl compounds; \u0000arenecarboxylic acids; \u00002,2′-bipyrroles; \u0000bridged and spirocyclic bicycloalkenones; \u0000ketones from halohydrins; \u0000arylation of quinones; \u0000cyclopropanation; \u00001,4-diacetoxylation of1,3-dienes; \u00001,4-acetoxytrifluoroacetoxylation of 1,3-dienes; \u0000vinylation of alkyl or aryl halides; \u0000β-aryl aldehydes; \u0000hydrogenolysis of allylic acetates; \u0000enones; \u0000ortho-alkylation of acetanilides; \u0000arylation of cycloalkenes; \u0000allylic acetoxylation; \u0000oxidative coupling of alkenylstannanes; \u0000lactonization of dienes by 1,4-functionation; \u00001,3,5-trienes; \u0000cyclization of o-iodophenyl allyl ethers to benzofurans; \u0000coupling of CH2CHSi(CH3)3 with vinyl iodides; \u0000vinylation of cycloalkenes; \u0000arylannelation of 1,3-dienes; \u0000coupling of ArI and unsaturated epoxides; \u0000bicyclic acetals; \u00001,4-additions to1,3-dienes; \u0000didehydroamino acids; \u0000cyclopentenones from carbohydrates; \u00003-arylcycloalkenes; \u0000coupling of vinyl halides with allylic alcohols; \u0000cyclization of 4,6- and 5,7-dieneamides; \u0000oxaspirocyclic addition to 1,3-dienes; \u0000RCH2CHO  RCHCHOCH3  RCHCHCHO; \u0000heck cyclization; \u0000heck-type coupling of allylic alcohols and enol triflates; \u0000coupling of vinyl halides with allyl alcohols; \u0000arylation of allylic alcohols; \u0000hydroacetoxylation of 2-alkynoates; \u0000three-component coupling of alkenes; \u0000heck reaction; \u0000suzuki, stille, and related couplings; \u0000reductive acylation and transesterification; \u00002-benzenesulfenyl-1,3-dienes; \u0000allylic oxidation; \u00001,4-difunctionalization of 1,3-dienes; \u0000cycloisomerization of enynes; \u0000heck reaction; \u0000arylation with onium salts; \u0000suzuki couplings; \u0000carboxylation; \u0000addition to multiple bonds; \u0000oxidation; \u0000heck reaction and other couplings; \u0000addition to multiple bonds; \u0000dehydrogenation of carbonyl compounds; \u0000indoles; \u0000cyclopropanation; \u0000enol ethers; \u0000coupling reactions; \u0000reactions of alkynes; \u0000carbonyl compounds; \u0000miscellaneous reactions; \u0000hydroarylation; \u0000carboxylation; \u0000rearrangement-coupling; \u0000conjugate addition; \u0000coupling reactions; \u0000redox reactions; \u0000vinyl glycosides; \u0000cyclizations; \u0000additions; \u0000allylic displacements; \u0000cyclopropanation; \u0000coupling reactions; \u0000addition reactions; \u0000cyclization reactions; \u0000cyclopentadienone acetals; \u0000oxidation; \u0000ketone synthesis; \u0000racemization; \u0000transan","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"15 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":"74101192","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-carbene complexes Rhodium-carbene复合物
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11904.PUB2
T. Ho, M. Fieser, L. Fieser
{"title":"Rhodium-carbene complexes","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS11904.PUB2","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11904.PUB2","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000rhenium(VII) oxide; \u0000Rh/alumina catalyst hydrogenation; \u0000rhodium - iron; \u0000rhodium(I) hexafluoroantimonate; \u0000ruthenium(III) chloride hydrate","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"1072 1","pages":"418-419"},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76682662","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) Chloride 铁(III)氯
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11421.PUB4
T. Ho, M. Fieser, L. Fieser
{"title":"Iron(III) Chloride","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS11421.PUB4","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11421.PUB4","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000reduction; \u0000substitutions; \u0000homoallylic ethers; \u0000Michael reaction; \u0000condensations; \u0000deacetalization; \u0000arylation; \u0000friedel—crafts reactions; \u0000cyclization reactions; \u0000addition and cycloaddition; \u0000substitution; \u0000substitution; \u0000addition; \u0000condensation; \u0000redox reactions; \u0000friedel–crafts reactions; \u0000other annulations; \u0000organoindium reagents; \u0000N-Functionalization; \u0000indium(III) bromide; \u0000skeletal reorganization; \u0000iodosuccinimide, NIS","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"43 4 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":"90721658","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
2,8,9‐Trialkyl‐1‐phospha‐2,5,8,9‐tetraazabicyclo[3.3.3]undecanes 2,8,9‐Trialkyl‐1‐phospha‐2,5,8,9‐tetraazabicyclo[3] 3月undecanes
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS10048.PUB4
T. Ho
{"title":"2,8,9‐Trialkyl‐1‐phospha‐2,5,8,9‐tetraazabicyclo[3.3.3]undecanes","authors":"T. Ho","doi":"10.1002/9780471264194.FOS10048.PUB4","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS10048.PUB4","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000trans-stilbene epoxides; \u0000condensation reactions; \u0000alcohol–ester interchange; \u0000silylcyanations; \u0000coupling reactions; \u0000diaryl ethers; \u0000isomerization; \u0000condensation","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"4 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80746388","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
Tungsten Carbene and Carbyne Complexes 碳化钨和碳化钨配合物
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11101.PUB2
T. Ho, M. Fieser, L. Fieser
{"title":"Tungsten Carbene and Carbyne Complexes","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS11101.PUB2","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11101.PUB2","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000aminocarbene diels–alder reactions; \u0000intramolecular bis-alkyne annelations; \u0000cycloheptadienones; \u0000cyclopentannulation; \u0000alkyne metathesis; \u0000cycloadditions; \u00001-hydroxytetralins; \u0000dihydropyran formation; \u0000alkyne metathesis","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"11972 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":"80982213","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
Molybdenum(V) chloride 氯化钼(V)
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11872
T. Ho, M. Fieser, L. Fieser
{"title":"Molybdenum(V) chloride","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS11872","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11872","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000pinacolatoboron B-Benzylation; \u0000MMPP; \u0000manganese(III) acetate; \u0000manganation; \u0000molybdenum-carbyne complexes","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"9 1","pages":"1-3"},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87694077","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) chloride 氯化钯(II)
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS07690.PUB6
T. Ho, M. Fieser, L. Fieser, Rick Danheiser, William R. Roush, Janice Smith
{"title":"Palladium(II) chloride","authors":"T. Ho, M. Fieser, L. Fieser, Rick Danheiser, William R. Roush, Janice Smith","doi":"10.1002/9780471264194.FOS07690.PUB6","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS07690.PUB6","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000π-allylpalladium complexes; \u0000phenolic coupling; \u0000asymmetric allylic alkylations; \u0000π-allylpalladium chloride dimers; \u0000reactions of allene catalyzed by palladium or rhodium compounds; \u0000aryl isocyanates; \u0000dehydrogenation; \u0000π-allylpalladium chloride dimers; \u0000alkylation of π-allylpalladium complexes; \u0000π-allylpalladium chloride dimers of α,β-unsaturated ketones; \u0000hydrolysis of nitriles to amides; \u0000pyridine- and quinolinecarboxylic acids; \u0000carbodiimides; \u0000polymer-supported reagent; \u0000π-allylpalladium dimers; \u0000oxidation of primary amines; \u0000polymer-supported reagent; \u00001,3-dienes; \u0000α,β-unsaturated ketosteroids; \u0000γ,δ-unsaturated sulfones; \u0000phenylation of enones; \u0000polymer-bound reagent; \u00001,5-dienes from π-allylpalladium chloride dimers; \u0000thallation–carbonylation; \u0000acetoxylation of β,γ-unsaturated esters; \u0000cyclization–insertion; \u0000wacker oxidation; \u0000carbonylation of (π-allyl)palladium dimers; \u0000coupling of π-(allylic)palladium complexes with an alkenylzirconium(IV) complex;1,4-dienes; \u0000(Z)-Δ3-alkenyl sulfones; \u0000α,β-unsaturated carbonyl compounds; \u0000allyl–allyl coupling; \u0000cyclization of hydroxyalkenes to furanes and pyranes; \u0000conjugate addition of 2-bromoarylmercury compounds; \u0000pyranosides cyclohexanones; \u00002,5-disubstituted tetrahydrofurans; \u0000reduction; \u0000acetals; \u0000o-Hydroxybenzophenones; \u0000cross-couplings; \u0000coupling reactions; \u0000arylation of salicylaldehydes; \u0000deallylation; \u0000halosilanes; \u0000hydrogenation; \u0000coupling reactions; \u0000oxidation; \u0000aziridines; \u0000coupling reactions; \u0000hydroarylation; \u0000coupling reactions; \u0000oxidation of alkenes; \u0000o-hydroxybenzyl ethers; \u0000benzhydryl ethers; \u0000alkylation; \u0000coupling reactions; \u0000cyclopentenones; \u0000reduction; \u0000addition; \u0000substitution; \u0000coupling reactions; \u0000oxidation; \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":"43 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":"88606189","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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