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Organic Syntheses最新文献

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Preparation of Radical Clocks Bearing Carbonyl Groups: Synthesis of N-Methoxy-N-methylspiro[cyclopropane-1,9'-fluorene]-2-carboxamide. 含羰基的辐射钟的制备：合成 N-甲氧基-N-甲基螺[环丙烷-1,9'-芴]-2-甲酰胺。
IF 0.7
Organic Syntheses Pub Date : 2024-01-01 Epub Date: 2024-03-23 DOI: 10.15227/orgsyn.101.0061
Nicole D Bartolo, Ryan N Robson, Collin H Witt, K A Woerpel
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引用次数: 0
Synthesis of Benzyl-δ-Truxinate via Enantioselective [2+2] Photocycloaddition. 通过对映体选择性 [2+2] 光环加成法合成苄基-δ-三嗪酸。
IF 0.7
Organic Syntheses Pub Date : 2024-01-01
Rodrigo Villanueva, Ellie F Plachinski, Tehshik P Yoon
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引用次数: 0
Synthesis of 4-(2,2-Difluorovinyl)benzonitrile through a Wittig-type Olefination of 4-Formylbenzonitrile.
IF 0.7
Organic Syntheses Pub Date : 2024-01-01 DOI: 10.15227/orgsyn.101.0542
Andrew J Intelli, Jacob P Sorrentino, Ryan A Altman
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引用次数: 0
Synthesis of Enantioenriched NH-Sulfoximines by NH Transfer to Sulfoxides Using Ammonium Carbamate and (Diacetoxyiodo)benzene 氨基甲酸铵和(二乙酰氧基)苯催化氨转移合成对映体富集的NH-亚砜胺
IF 0.7
Organic Syntheses Pub Date : 2023-01-01 DOI: 10.15227/orgsyn.0100.0186
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引用次数: 1
α-Arylation of Cyclopentanones by Palladium/Enamine Cooperative Catalysis 钯/烯胺协同催化环戊酮α-芳基化研究
IF 0.7
Organic Syntheses Pub Date : 2023-01-01 DOI: 10.15227/orgsyn.100.0099
Yibin Xue
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引用次数: 0
Synthesis of NH-Sulfoximines from Sulfides Using Ammonium Carbamate and (Diacetoxyiodo)benzene to Transfer NH and O 氨基甲酸铵和(二乙酰氧基)苯转移nhh和O从硫化物中合成NH-亚砜亚胺
IF 0.7
Organic Syntheses Pub Date : 2023-01-01 DOI: 10.15227/orgsyn.100.0048
Arianna Tota
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引用次数: 1
N-(Benzyloxy)-N-(pivaloyloxy)-4-(trifluoromethyl)-benzamide N - (Benzyloxy) - N - (pivaloyloxy) 4 -苯甲酰胺(trifluoromethyl)
IF 0.7
Organic Syntheses Pub Date : 2023-01-01 DOI: 10.15227/orgsyn.100.0113
Kathleen J. Berger
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引用次数: 0
Preparation of Pyrylium Tetrafluoroborate (Pyry-BF4) 四氟硼酸Pyry-BF4的制备
Organic Syntheses Pub Date : 2023-01-01 DOI: 10.15227/orgsyn.100.0361
Alejandro Gómez Palomino
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引用次数: 0
Discussion Addendum for: Indium‐Catalyzed Heteroaryl–Heteroaryl Bond Formation through Nucleophilic Aromatic Substitution: Preparation of 2‐Methyl-3-(thien-2‐yl)‐1H-indole 讨论附录:铟催化通过亲核芳香取代形成杂芳基键:制备2 -甲基-3-(噻吩-2 -基)- 1h -吲哚
Organic Syntheses Pub Date : 2023-01-01 DOI: 10.15227/orgsyn.100.0287
Teruhisa Tsuchimoto
{"title":"Discussion Addendum for: Indium‐Catalyzed Heteroaryl–Heteroaryl Bond Formation through Nucleophilic Aromatic Substitution: Preparation of 2‐Methyl-3-(thien-2‐yl)‐1H-indole","authors":"Teruhisa Tsuchimoto","doi":"10.15227/orgsyn.100.0287","DOIUrl":"https://doi.org/10.15227/orgsyn.100.0287","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":"273 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":"135596986","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 Diethyl (1-Diazo-2-oxopropyl)phosphonate 磷酸二乙酯(1-重氮-2-氧丙基)的合成
IF 0.7
Organic Syntheses Pub Date : 2023-01-01 DOI: 10.15227/orgsyn.100.0084
Cholapat Varongchayakul
{"title":"Synthesis of Diethyl (1-Diazo-2-oxopropyl)phosphonate","authors":"Cholapat Varongchayakul","doi":"10.15227/orgsyn.100.0084","DOIUrl":"https://doi.org/10.15227/orgsyn.100.0084","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":"67342638","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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