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Synthesis of 4‐Methylbenzoate(2′,4′,6′‐Trimethoxy‐Phenyl)Iodonium Tosylate 4‐苯甲酸甲酯(2′，4′，6′‐三甲氧基苯基)碘磺酸盐的合成
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2020-04-29 DOI: 10.1002/0471264229.os096.10
Thomas L. Seidl, A. Moment, C. Orella, T. Vickery, David R. Stuart
{"title":"Synthesis of 4‐Methylbenzoate(2′,4′,6′‐Trimethoxy‐Phenyl)Iodonium Tosylate","authors":"Thomas L. Seidl, A. Moment, C. Orella, T. Vickery, David R. Stuart","doi":"10.1002/0471264229.os096.10","DOIUrl":"https://doi.org/10.1002/0471264229.os096.10","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":"1 1","pages":"1-13"},"PeriodicalIF":0.7,"publicationDate":"2020-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43320420","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
Synthesis of Chiral Diamine Ligands for Nickel‐Catalyzed Asymmetric Cross‐Couplings of Alkylchloroboronate Esters with Alkylzincs: (1 R ,2 R )‐ N , N ′‐Dimethyl‐1,2‐Bis(2‐Methylphenyl)‐1,2‐Diaminoethane 镍催化烷基氯硼酸酯与烷基锌不对称交叉偶联的手性二胺配体的合成:(1r, 2r)‐N, N′‐二甲基‐1,2‐双(2‐甲基苯基)‐1,2‐二氨基乙烷
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2020-04-29 DOI: 10.1002/0471264229.os096.16
Yusuke Masuda, G. C. Fu, Skyler D Mendoza, S. Reisman
{"title":"Synthesis of Chiral Diamine Ligands for Nickel‐Catalyzed Asymmetric Cross‐Couplings of Alkylchloroboronate Esters with Alkylzincs: (1\u0000 R\u0000 ,2\u0000 R\u0000 )‐\u0000 N\u0000 ,\u0000 N\u0000 ′‐Dimethyl‐1,2‐Bis(2‐Methylphenyl)‐1,2‐Diaminoethane","authors":"Yusuke Masuda, G. C. Fu, Skyler D Mendoza, S. Reisman","doi":"10.1002/0471264229.os096.16","DOIUrl":"https://doi.org/10.1002/0471264229.os096.16","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":" ","pages":""},"PeriodicalIF":0.7,"publicationDate":"2020-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46182782","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
Discussion Addendum for: Preparation of Enantioenriched Homoallylic Primary Amines 讨论附录:富集对映体的同丙烯基伯胺的制备
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2020-04-29 DOI: 10.1002/0471264229.OS096.12
M. Yus
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引用次数: 2
Gold‐Catalyzed Oxidative Coupling of Arenes and Arylsilanes 金催化芳烃和芳基硅烷的氧化偶联
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2020-04-29 DOI: 10.1002/0471264229.OS096.11
Chris Nottingham, Verity Barber, G. Lloyd‐Jones, Alexandre Genoux, E. Merino, Cristina Nevado
{"title":"Gold‐Catalyzed Oxidative Coupling of Arenes and Arylsilanes","authors":"Chris Nottingham, Verity Barber, G. Lloyd‐Jones, Alexandre Genoux, E. Merino, Cristina Nevado","doi":"10.1002/0471264229.OS096.11","DOIUrl":"https://doi.org/10.1002/0471264229.OS096.11","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":" ","pages":""},"PeriodicalIF":0.7,"publicationDate":"2020-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49259086","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
Synthesis of Chiral Tetramic Acids: Preparation of ( S )‐5‐Benzylpyrrolidine‐2,4‐Dione from L‐Phenylalanine Methyl Ester Hydrochloride 手性四羧酸的合成:L -苯丙氨酸甲酯盐酸盐制备(S)‐5‐苄基吡咯烷‐2,4‐二酮
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2020-04-29 DOI: 10.1002/0471264229.os096.32
Kyle M. Lambert, Austin W. Medley, Amy C. Jackson, Lauren E Markham, John L. Wood, Anna C. Impastato, D. Trauner
{"title":"Synthesis of Chiral Tetramic Acids: Preparation of (\u0000 S\u0000 )‐5‐Benzylpyrrolidine‐2,4‐Dione from L‐Phenylalanine Methyl Ester Hydrochloride","authors":"Kyle M. Lambert, Austin W. Medley, Amy C. Jackson, Lauren E Markham, John L. Wood, Anna C. Impastato, D. Trauner","doi":"10.1002/0471264229.os096.32","DOIUrl":"https://doi.org/10.1002/0471264229.os096.32","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":" ","pages":""},"PeriodicalIF":0.7,"publicationDate":"2020-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48450916","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
Catalytic Enantioselective Addition of an In‐Situ Prepared Aryltitanium Reagent to p ‐Chloroacetophenone: ( R )‐(+)‐1‐(4‐Chlorophenyl)‐1‐ m ‐Tolylethanol 原位制备芳基钛试剂对对氯苯乙酮的催化对映选择性加成:(R)‐(+)‐1‐(4‐氯苯基)‐1‐m‐甲苯乙醇
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2020-04-29 DOI: 10.1002/0471264229.OS096.21
Yusuke Kobayashi, A. Matsuda, Tomoya Ushimaru, T. Harada, J. Hughes, K. Campos
{"title":"Catalytic Enantioselective Addition of an In‐Situ Prepared Aryltitanium Reagent to\u0000 p\u0000 ‐Chloroacetophenone: (\u0000 R\u0000 )‐(+)‐1‐(4‐Chlorophenyl)‐1‐\u0000 m\u0000 ‐Tolylethanol","authors":"Yusuke Kobayashi, A. Matsuda, Tomoya Ushimaru, T. Harada, J. Hughes, K. Campos","doi":"10.1002/0471264229.OS096.21","DOIUrl":"https://doi.org/10.1002/0471264229.OS096.21","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":"127 1","pages":""},"PeriodicalIF":0.7,"publicationDate":"2020-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"50943877","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
Discussion Addendum for: Synthesis of Ynamides by Copper-Mediated Coupling of 1,1-Dibromo-1-Alkenes with Nitrogen Nucleophiles. Preparation of 4-Methyl-N-(2-Phenylethynyl)-N-(Phenylmethyl)Benzenesulfonamide 讨论附录:铜介导1,1-二溴-1-烯烃与氮亲核试剂偶联合成酰胺。4-甲基- n -(2-苯基乙基)- n -(苯基甲基)苯磺酰胺的制备
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2020-04-29 DOI: 10.1002/0471264229.os096.13
Cédric Theunissen, Pierre Thilmany, Mounsef Lahboubi, N. Blanchard, G. Evano
{"title":"Discussion Addendum for: Synthesis of Ynamides by Copper-Mediated Coupling of 1,1-Dibromo-1-Alkenes with Nitrogen Nucleophiles. Preparation of 4-Methyl-N\u0000-(2-Phenylethynyl)-N\u0000-(Phenylmethyl)Benzenesulfonamide","authors":"Cédric Theunissen, Pierre Thilmany, Mounsef Lahboubi, N. Blanchard, G. Evano","doi":"10.1002/0471264229.os096.13","DOIUrl":"https://doi.org/10.1002/0471264229.os096.13","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":" ","pages":""},"PeriodicalIF":0.7,"publicationDate":"2020-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44936590","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
( R )‐ N,N '‐Dimethyl‐1,1'‐Binaphthyldiamine (R)‐N, N 110毫克‐‐”‐Binaphthyldiamine
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2020-04-29 DOI: 10.1002/0471264229.os096.24
S. Denmark, P. Ryabchuk, Eric R. Welin, B. Stoltz
{"title":"(\u0000 R\u0000 )‐\u0000 N,N\u0000 '‐Dimethyl‐1,1'‐Binaphthyldiamine","authors":"S. Denmark, P. Ryabchuk, Eric R. Welin, B. Stoltz","doi":"10.1002/0471264229.os096.24","DOIUrl":"https://doi.org/10.1002/0471264229.os096.24","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":"7 ","pages":""},"PeriodicalIF":0.7,"publicationDate":"2020-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"50944039","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
Synthesis of 3,6-Bis(dimethylamino)-9H-xanthen-9-one by Stepwise Chemical Redox Cycling 逐步化学氧化还原循环合成3,6-二(二甲氨基)- 9h -杂原-9- 1
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2020-01-01 DOI: 10.15227/orgsyn.097.0021
J. Bachman
{"title":"Synthesis of 3,6-Bis(dimethylamino)-9H-xanthen-9-one by Stepwise Chemical Redox Cycling","authors":"J. Bachman","doi":"10.15227/orgsyn.097.0021","DOIUrl":"https://doi.org/10.15227/orgsyn.097.0021","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":"1 1","pages":""},"PeriodicalIF":0.7,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67338969","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
Discussion Addendum for: (S)-(-)-2-Allylcyclohexanone (2-Allylcyclohexan-1-one] (S)-(-)-2-烯丙基环己酮(2-烯丙基环己酮-1- 1)的讨论附录
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2020-01-01 DOI: 10.15227/orgsyn.097.0079
M. Braun
{"title":"Discussion Addendum for: (S)-(-)-2-Allylcyclohexanone (2-Allylcyclohexan-1-one]","authors":"M. Braun","doi":"10.15227/orgsyn.097.0079","DOIUrl":"https://doi.org/10.15227/orgsyn.097.0079","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":"115 1","pages":"79-95"},"PeriodicalIF":0.7,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67339290","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: 2
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