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Organic Syntheses最新文献

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Visible-light-mediated Oxidative Debenzylation of 3-O-Benzyl-1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 可见光介导的3- o -苄基-1,2:5,6-二- o -异丙基-α- d -葡萄糖醛酸氧化脱苯反应
IF 0.7
Organic Syntheses Pub Date : 2023-01-01 DOI: 10.15227/orgsyn.100.0271
Amiera Madani
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引用次数: 0
Discussion Addendum for: Rh(I)-Catalyzed Allenic Pauson–Khand Reaction 讨论附录:Rh(I)催化的异丙烯Pauson-Khand反应
IF 0.7
Organic Syntheses Pub Date : 2023-01-01 DOI: 10.15227/orgsyn.100.0029
Eric D. Deihl
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引用次数: 0
Synthesis of Phenols from Benzoic Acids 苯甲酸合成酚类化合物
IF 0.7
Organic Syntheses Pub Date : 2023-01-01 DOI: 10.15227/orgsyn.100.0199
Wenzhang Xiong
{"title":"Synthesis of Phenols from Benzoic Acids","authors":"Wenzhang Xiong","doi":"10.15227/orgsyn.100.0199","DOIUrl":"https://doi.org/10.15227/orgsyn.100.0199","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":"1 1","pages":""},"PeriodicalIF":0.7,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67342979","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
Visible-Light-Promoted C-S Cross-Coupling Reaction for Synthesis of Aromatic Thioethers. 用可见光促进 C-S 交叉偶联反应合成芳香族硫醚。
IF 0.7
Organic Syntheses Pub Date : 2023-01-01 Epub Date: 2023-06-15 DOI: 10.15227/orgsyn.100.0234
Yingjun Lan, Junhua Xu, Chern-Hooi Lim, Garret M Miyake, Bin Liu
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引用次数: 0
Synthesis of 2-Phenyl-4,6-bis(trifluoromethyl)pyridine via NH4I/Na2S2O4-Mediated Cyclization of Ketoxime Acetates NH4I/ na2s2o4介导醋酸酮肟环化合成2-苯基-4,6-双(三氟甲基)吡啶
IF 0.7
Organic Syntheses Pub Date : 2023-01-01 DOI: 10.15227/orgsyn.100.0248
Huawen Huang
{"title":"Synthesis of 2-Phenyl-4,6-bis(trifluoromethyl)pyridine via NH4I/Na2S2O4-Mediated Cyclization of Ketoxime Acetates","authors":"Huawen Huang","doi":"10.15227/orgsyn.100.0248","DOIUrl":"https://doi.org/10.15227/orgsyn.100.0248","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":"1 1","pages":""},"PeriodicalIF":0.7,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67343020","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
Preparation of 4-(5-(p-Tolyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)benzenesulfonyl fluoride (ArSO2F) 4-(5-(对甲苯基)-3-(三氟甲基)- 1h -吡唑-1-基)苯磺酰氟(ArSO2F)的制备
Organic Syntheses Pub Date : 2023-01-01 DOI: 10.15227/orgsyn.100.0382
Lucas Wagner
{"title":"Preparation of 4-(5-(p-Tolyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)benzenesulfonyl fluoride (ArSO2F)","authors":"Lucas Wagner","doi":"10.15227/orgsyn.100.0382","DOIUrl":"https://doi.org/10.15227/orgsyn.100.0382","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":"95 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135211257","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
Preparation of (S)-3,3ʹ-Bis(1-pyrrolidinylmethyl)-5,5ʹ,6,6ʹ, 7,7ʹ,8,8ʹ-octahydro-1,1'-bi-2-naphthol 制备(S)-3,3ʹ-双(1-吡咯烷甲基)-5,5ʹ,6,6ʹ, 7,7ʹ,8,8ʹ-八氢-1,1'-联-2-萘酚
Organic Syntheses Pub Date : 2023-01-01 DOI: 10.15227/orgsyn.100.0394
Yu Hong
{"title":"Preparation of (S)-3,3ʹ-Bis(1-pyrrolidinylmethyl)-5,5ʹ,6,6ʹ, 7,7ʹ,8,8ʹ-octahydro-1,1'-bi-2-naphthol","authors":"Yu Hong","doi":"10.15227/orgsyn.100.0394","DOIUrl":"https://doi.org/10.15227/orgsyn.100.0394","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":"19 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135213971","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
Stereoselective Synthesis of (E)-Vinylstannanes from Alkynes via Hydroboration and Transmetalation 硼氢化和转金属法制备炔基(E)-乙烯基锡烷
Organic Syntheses Pub Date : 2023-01-01 DOI: 10.15227/orgsyn.100.0327
Ruiyang Guo
{"title":"Stereoselective Synthesis of (E)-Vinylstannanes from Alkynes via Hydroboration and Transmetalation","authors":"Ruiyang Guo","doi":"10.15227/orgsyn.100.0327","DOIUrl":"https://doi.org/10.15227/orgsyn.100.0327","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":"81 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136205474","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 4-Phenylpyrrolidin-2-one via an Aza-Baeyer-Villiger Rearrangement Aza-Baeyer-Villiger重排法合成4-苯基吡咯烷-2- 1
Organic Syntheses Pub Date : 2023-01-01 DOI: 10.15227/orgsyn.100.0347
Mike Ong
{"title":"Synthesis of 4-Phenylpyrrolidin-2-one via an Aza-Baeyer-Villiger Rearrangement","authors":"Mike Ong","doi":"10.15227/orgsyn.100.0347","DOIUrl":"https://doi.org/10.15227/orgsyn.100.0347","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":"46 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136258015","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
Preparation of Highly-Substituted Pyridines via Diels-Alder Reactions of Vinylallenes and Tosyl cyanide 乙烯烯与甲酰基氰化物diel - alder反应制备高取代吡啶
IF 0.7
Organic Syntheses Pub Date : 2023-01-01 DOI: 10.15227/orgsyn.100.0004
Nathan H. Faialaga
{"title":"Preparation of Highly-Substituted Pyridines via Diels-Alder Reactions of Vinylallenes and Tosyl cyanide","authors":"Nathan H. Faialaga","doi":"10.15227/orgsyn.100.0004","DOIUrl":"https://doi.org/10.15227/orgsyn.100.0004","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":"1 1","pages":""},"PeriodicalIF":0.7,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67342609","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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