首页 > 最新文献

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

英文 中文
Iron(II) Sulfide 铁(II)硫化
Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11749
T. Ho, M. Fieser, L. Fieser
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
第1部分:产品和公司标识硫化铁(II)同义词/通用名称:硫化亚铁产品用途:仅供教育用途制造商:Columbus Chemical Industries, Inc., Columbus, WI 53925。24小时紧急信息电话:CHEMTREC(美国):800-424-9300 CANUTEC(加拿大):613-424-6666 ScholAR Chemistry;5100 W。亨利埃塔路,罗切斯特,纽约14586;(866) 260 - 0501;www.Scholarchemistry.com
{"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
Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11844.PUB2
T. Ho
This article has no abstract. Keywords: Baylis-Hillman reaction; cycloisomerization; dibutylboron alkoxides and dicarboxylates; 4,5-Dichlorophthaloyl peroxide; dimethyldioxirane, DMDO
这篇文章没有摘要。关键词:Baylis-Hillman反应;cycloisomerization;二丁基硼烷氧化物和二羧酸盐;4, 5-Dichlorophthaloyl过氧化;dimethyldioxirane, DMDO
{"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
Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS09963.PUB4
T. Ho, M. Fieser, L. Fieser
This article has no abstract. Keywords: alkenes; desulfurative silylation; cyclopentenones; alkenation; n-arylpyrrolidines; cyclopropanes; coupling reactions; polyene synthesis; homopropargylic alcohols; conjugated dienes; tetrabutylammonium fluoride, TBAF; tetrabutylammonium difluorotriphenylsilicate; tetracarbonylhydridorhenium; titanocene bis(triethyl phosphite); trimethylsilyl trifluoromethanesulfonate
这篇文章没有摘要。关键词:烯烃;desulfurative甲硅烷基化;环戊烯酮;alkenation;n-arylpyrrolidines;环丙烷;耦合反应;多烯合成;homopropargylic醇;共轭二烯烃;四丁基氟化铵;四丁铵difluorotriphenylsilicate;tetracarbonylhydridorhenium;二茂钛二亚磷酸三乙酯;三甲基硅烷基trifluoromethanesulfonate
{"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
Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11451.PUB5
T. Ho, M. Fieser, L. Fieser
This article has no abstract. Keywords: N-arylation; coupling reactions; allylation; ketone synthesis; arylation; functionalized arenes; coupling reactions; homoallylic amines; cycloadditions; rearrangement; suzuki coupling; decarboxylative coupling; arylation and alkenylation; miscellaneous coupling reactions; allylation; carbonylation; addition and cycloaddition; rearrangement; review; substitution; coupling reactions; annulation; rearrangement; tetrabutylammonium fluoride, TBAF; tetrabutylammonium difluorotriphenylsilicate; tetracarbonylhydridorhenium; titanocene bis(triethyl phosphite); trimethylsilyl trifluoromethanesulfonate
这篇文章没有摘要。关键词:N-arylation;耦合反应;烯丙基化;酮的合成;芳基化;功能化芳烃;耦合反应;homoallylic胺;环加;重排;铃木耦合;decarboxylative耦合;芳基化和烯基化;杂偶联反应;烯丙基化;羰基化反应;加成和环加成;重排;审查;替换;耦合反应;环状结构;重排;四丁基氟化铵;四丁铵difluorotriphenylsilicate;tetracarbonylhydridorhenium;二茂钛二亚磷酸三乙酯;三甲基硅烷基trifluoromethanesulfonate
{"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)
Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS09647
T. Ho, Mary Fieser, R. Danheiser, W. Roush, L. Fieser
This article has no abstract. Keywords: preparation; alkenyl–aryl coupling; phenanthrene synthesis; coupling of vinyl chlorides with grignard reagents; ArCN; coupling reactions
这篇文章没有摘要。关键词:准备;alkenyl-aryl耦合;菲合成;氯乙烯与格氏试剂的偶联ArCN;耦合反应
{"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)
Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11349
T. Ho, M. Fieser, L. Fieser
This article has no abstract. Keywords: diels–alder reactions; C-Alkylation; 1,8-diarylnaphthalenes; coupling of aryl O-carbamates and aryl triflates with RMgCl; β-enamino lactones; carbozincation; biphenyls; 1,2-syn addition to alkynes; homocouplings; cross-couplings; conjugate additions; [4 + 2]cycloaddition; cross couplings; organometallic reactions of carbonyl compounds; addition-coupling sequences; cross-couplings; N-arylation; homoallylation; [2 + 2 + 2]cycloaddition; 1,4-silaboration; alkylations; (E)-allylsilanes; coupling reactions; hydrophosphinylation; coupling; Coupling; reductive michael addition; reduction of imines; coupling; n-arylation; addition
这篇文章没有摘要。关键词:dieles - alder反应;C-Alkylation;1、8-diarylnaphthalenes;邻氨基甲酸芳酯和三氟甲酸芳酯与RMgCl的偶联β-enamino内酯;carbozincation;联苯;1,2-syn炔烃加成;homocouplings;他们;共轭增加;[4 + 2]环加成;交叉耦合;羰基化合物的有机金属反应;addition-coupling序列;他们;N-arylation;homoallylation;[2 + 2 + 2]环加成;1、4-silaboration;烷基化;(E) -allylsilanes;耦合反应;hydrophosphinylation;耦合;耦合;还原迈克尔加法;亚胺的还原;耦合;n-arylation;除了
{"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)]
Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11706.PUB2
T. Ho, Mary Fieser, Louis Fieser
This article has no abstract. Keywords: hydroamination; cycloaddition; 2-Benzothiazolylmethyl 2-oxoalkyl sulfones; hydroaminomethylation to alkenes; BINAMINE derivatives; BINOL-derived phosphites; cyclobutanol cleavage
这篇文章没有摘要。关键词:hydroamination;环加成作用;2-苯并噻唑基甲基2-氧烷基砜;氢胺甲基化制烯烃;BINAMINE衍生品;BINOL-derived亚磷酸盐;环丁醇乳沟
{"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)
Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11636.PUB2
T. Ho, M. Fieser, L. Fieser
This article has no abstract. Keywords: hydroxymethylation; oxidation; silylation; aminolysis; demetallation
这篇文章没有摘要。关键词:hydroxymethylation;氧化;甲硅烷基化;氨解;demetallation
{"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
Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11417.PUB3
T. Ho, M. Fieser, L. Fieser
This article has no abstract. Keywords: cyclization; cycloaddition; Friedel-Crafts alkylations; Meyer-Schuster Rearrangement; cyclizations; transglycosylation; condensation; O-trimethylsilyl cyanohydrins; insertion by nitrene; cyclization; substitution; quinoline synthesis; benzyl ethers; cyclization; cycloaddition; Friedel-Crafts alkylations; Meyer-Schuster Rearrangement; cyclizations; transglycosylation; condensation; O-trimethylsilyl cyanohydrins; insertion by nitrene; cyclization; substitution; quinoline synthesis; benzyl ethers; gallium(III) chloride; Friedel-Crafts reaction; Sonogashira coupling; Grignard reagents/cobalt(II) salts; Gold(III) chloride – silver salts
这篇文章没有摘要。关键词:环化;环加成作用;傅克烷基化;Meyer-Schuster重排;环化;转糖基作用;凝结;O-trimethylsilyl氰醇;亚硝基插入;环化;替换;喹啉合成;苄醚;环化;环加成作用;傅克烷基化;Meyer-Schuster重排;环化;转糖基作用;凝结;O-trimethylsilyl氰醇;亚硝基插入;环化;替换;喹啉合成;苄醚;氯化镓(III);傅克反应;Sonogashira耦合;格氏试剂/钴(II)盐;氯化金(III)银盐
{"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
Pub Date : 2017-02-21 DOI: 10.1002/9780471264194.FOS11806.PUB2
T. Ho, M. Fieser, L. Fieser
This article has no abstract. Keywords: hydroaminoalkylation; organozinc reagents; hydriodination; reductive amination; Arbuzov reaction; zirconium(IV) dimethylamide
这篇文章没有摘要。关键词:hydroaminoalkylation;organozinc试剂;hydriodination;还原胺化作用;Arbuzov反应;锆(IV) dimethylamide
{"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
期刊
Fieser and Fieser's Reagents for Organic Synthesis
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1