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

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Iron(II) Sulfide 铁(II)硫化
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11749
T. Ho, M. Fieser, L. Fieser
{"title":"Iron(II) Sulfide","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS11749","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11749","url":null,"abstract":"Section 1: Product and Company Identification Iron (II) Sulfide Synonyms/General Names: Ferrous Sulfide Product Use: For educational use only Manufacturer: Columbus Chemical Industries, Inc., Columbus, WI 53925. 24 Hour Emergency Information Telephone Numbers CHEMTREC (USA): 800-424-9300 CANUTEC (Canada): 613-424-6666 ScholAR Chemistry; 5100 W. Henrietta Rd, Rochester, NY 14586; (866) 260-0501; www.Scholarchemistry.com","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"77 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87753443","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
Difluoromethyl 2‐Pyridyl Sulfone 二氟甲基2 -吡啶基砜
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11844.PUB2
T. Ho
{"title":"Difluoromethyl 2‐Pyridyl Sulfone","authors":"T. Ho","doi":"10.1002/9780471264194.FOS11844.PUB2","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11844.PUB2","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000Baylis-Hillman reaction; \u0000cycloisomerization; \u0000dibutylboron alkoxides and dicarboxylates; \u00004,5-Dichlorophthaloyl peroxide; \u0000dimethyldioxirane, DMDO","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"156 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79848101","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
Titanocene Bis(Triethyl Phosphite) 二茂钛二亚磷酸三乙酯
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS09963.PUB4
T. Ho, M. Fieser, L. Fieser
{"title":"Titanocene Bis(Triethyl Phosphite)","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS09963.PUB4","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS09963.PUB4","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000alkenes; \u0000desulfurative silylation; \u0000cyclopentenones; \u0000alkenation; \u0000n-arylpyrrolidines; \u0000cyclopropanes; \u0000coupling reactions; \u0000polyene synthesis; \u0000homopropargylic alcohols; \u0000conjugated dienes; \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":"7 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":"73617933","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
Tris(dibenzylideneacetone)dipalladium
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11451.PUB5
T. Ho, M. Fieser, L. Fieser
{"title":"Tris(dibenzylideneacetone)dipalladium","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS11451.PUB5","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11451.PUB5","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000N-arylation; \u0000coupling reactions; \u0000allylation; \u0000ketone synthesis; \u0000arylation; \u0000functionalized arenes; \u0000coupling reactions; \u0000homoallylic amines; \u0000cycloadditions; \u0000rearrangement; \u0000suzuki coupling; \u0000decarboxylative coupling; \u0000arylation and alkenylation; \u0000miscellaneous coupling reactions; \u0000allylation; \u0000carbonylation; \u0000addition and cycloaddition; \u0000rearrangement; \u0000review; \u0000substitution; \u0000coupling reactions; \u0000annulation; \u0000rearrangement; \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":"74 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":"89376487","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
Tetrakis(triphenylphosphine)nickel(0) Tetrakis(三苯基膦)镍(0)
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS09647
T. Ho, Mary Fieser, R. Danheiser, W. Roush, L. Fieser
{"title":"Tetrakis(triphenylphosphine)nickel(0)","authors":"T. Ho, Mary Fieser, R. Danheiser, W. Roush, L. Fieser","doi":"10.1002/9780471264194.FOS09647","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS09647","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000preparation; \u0000alkenyl–aryl coupling; \u0000phenanthrene synthesis; \u0000coupling of vinyl chlorides with grignard reagents; \u0000ArCN; \u0000coupling reactions","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"3 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78683052","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
Nickel(II) acetylacetonate 乙酰丙酮镍(II)
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11349
T. Ho, M. Fieser, L. Fieser
{"title":"Nickel(II) acetylacetonate","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS11349","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11349","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000diels–alder reactions; \u0000C-Alkylation; \u00001,8-diarylnaphthalenes; \u0000coupling of aryl O-carbamates and aryl triflates with RMgCl; \u0000β-enamino lactones; \u0000carbozincation; \u0000biphenyls; \u00001,2-syn addition to alkynes; \u0000homocouplings; \u0000cross-couplings; \u0000conjugate additions; \u0000[4 + 2]cycloaddition; \u0000cross couplings; \u0000organometallic reactions of carbonyl compounds; \u0000addition-coupling sequences; \u0000cross-couplings; \u0000N-arylation; \u0000homoallylation; \u0000[2 + 2 + 2]cycloaddition; \u00001,4-silaboration; \u0000alkylations; \u0000(E)-allylsilanes; \u0000coupling reactions; \u0000hydrophosphinylation; \u0000coupling; \u0000Coupling; \u0000reductive michael addition; \u0000reduction of imines; \u0000coupling; \u0000n-arylation; \u0000addition","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"128 1","pages":"376-377"},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74601449","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[Chloro(Dicyclooctene)Rhodium(I)]
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11706.PUB2
T. Ho, Mary Fieser, Louis Fieser
{"title":"Bis[Chloro(Dicyclooctene)Rhodium(I)]","authors":"T. Ho, Mary Fieser, Louis Fieser","doi":"10.1002/9780471264194.FOS11706.PUB2","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11706.PUB2","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000hydroamination; \u0000cycloaddition; \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":"8 1","pages":"47-48"},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77893039","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) Nitrate 硝酸铁(III)
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11636.PUB2
T. Ho, M. Fieser, L. Fieser
{"title":"Iron(III) Nitrate","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS11636.PUB2","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11636.PUB2","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000hydroxymethylation; \u0000oxidation; \u0000silylation; \u0000aminolysis; \u0000demetallation","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"129 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79189296","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
Gold(III) Chloride 三氯化金
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11417.PUB3
T. Ho, M. Fieser, L. Fieser
{"title":"Gold(III) Chloride","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS11417.PUB3","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11417.PUB3","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000cyclization; \u0000cycloaddition; \u0000Friedel-Crafts alkylations; \u0000Meyer-Schuster Rearrangement; \u0000cyclizations; \u0000transglycosylation; \u0000condensation; \u0000O-trimethylsilyl cyanohydrins; \u0000insertion by nitrene; \u0000cyclization; \u0000substitution; \u0000quinoline synthesis; \u0000benzyl ethers; \u0000cyclization; \u0000cycloaddition; \u0000Friedel-Crafts alkylations; \u0000Meyer-Schuster Rearrangement; \u0000cyclizations; \u0000transglycosylation; \u0000condensation; \u0000O-trimethylsilyl cyanohydrins; \u0000insertion by nitrene; \u0000cyclization; \u0000substitution; \u0000quinoline synthesis; \u0000benzyl ethers; \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":"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":"76867532","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
Zirconium (IV) Dimethylamide 锆(IV)二甲酰胺
Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11806.PUB2
T. Ho, M. Fieser, L. Fieser
{"title":"Zirconium (IV) Dimethylamide","authors":"T. Ho, M. Fieser, L. Fieser","doi":"10.1002/9780471264194.FOS11806.PUB2","DOIUrl":"https://doi.org/10.1002/9780471264194.FOS11806.PUB2","url":null,"abstract":"This article has no abstract. \u0000 \u0000Keywords: \u0000 \u0000hydroaminoalkylation; \u0000organozinc reagents; \u0000hydriodination; \u0000reductive amination; \u0000Arbuzov reaction; \u0000zirconium(IV) dimethylamide","PeriodicalId":12135,"journal":{"name":"Fieser and Fieser's Reagents for Organic Synthesis","volume":"37 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2017-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90303738","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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