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Organic Syntheses最新文献

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Mild mono-Acylation of 4,5-Diiodoimidazole: Preparation of 1-(5-Iodo-1H-imidazole-4-yl)pent-4-en-1-one 4,5-二碘咪唑的轻度单酰化:1-(5-碘- 1h -咪唑-4-基)戊-4-烯-1- 1的制备
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2021-01-01 DOI: 10.15227/orgsyn.098.0171
M. Morgen
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引用次数: 1
Reductive Deuteration of Ketones with Magnesium and D2O for the Synthesis of α-Deutero-o-methyl-benzhydrol 镁和D2O对酮的还原氘化反应合成α-氘-邻甲基苯甲酸
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2021-01-01 DOI: 10.15227/ORGSYN.098.0051
Nengbo Zhu
{"title":"Reductive Deuteration of Ketones with Magnesium and D2O for the Synthesis of α-Deutero-o-methyl-benzhydrol","authors":"Nengbo Zhu","doi":"10.15227/ORGSYN.098.0051","DOIUrl":"https://doi.org/10.15227/ORGSYN.098.0051","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":"98 1","pages":"51-67"},"PeriodicalIF":0.7,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67340071","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 1-Hydrosilatrane, and Its Use in the Highly Practical Synthesis of Secondary and Tertiary Amines from Aldehydes and Ketones via Direct Reductive Amination 1-氢硅烷的制备及其在醛酮直接还原胺化合成仲胺和叔胺中的应用
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2021-01-01 DOI: 10.15227/orgsyn.098.0227
F. Azam
{"title":"Preparation of 1-Hydrosilatrane, and Its Use in the Highly Practical Synthesis of Secondary and Tertiary Amines from Aldehydes and Ketones via Direct Reductive Amination","authors":"F. Azam","doi":"10.15227/orgsyn.098.0227","DOIUrl":"https://doi.org/10.15227/orgsyn.098.0227","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":"1 1","pages":""},"PeriodicalIF":0.7,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67340367","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
Preparation of 6-(Triethylsilyl)cyclohex-1-en-1-yl Trifluoromethanesulfonate 6-(三乙基硅基)环己基-1-烯-1-基三氟甲烷磺酸盐的制备
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2021-01-01 DOI: 10.15227/orgsyn.098.0407
R. Nakura
{"title":"Preparation of 6-(Triethylsilyl)cyclohex-1-en-1-yl Trifluoromethanesulfonate","authors":"R. Nakura","doi":"10.15227/orgsyn.098.0407","DOIUrl":"https://doi.org/10.15227/orgsyn.098.0407","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":"1 1","pages":""},"PeriodicalIF":0.7,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67340491","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 1-Benzyl-7-methylene-1,5,6,7-tetrahydro-4H-benzo[d]imidazol-4-one 1-苄基-7-亚甲基-1,5,6,7-四氢- 4h -苯并咪唑-4-酮的制备
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2021-01-01 DOI: 10.15227/orgsyn.098.0315
M. Morgen
{"title":"Preparation of 1-Benzyl-7-methylene-1,5,6,7-tetrahydro-4H-benzo[d]imidazol-4-one","authors":"M. Morgen","doi":"10.15227/orgsyn.098.0315","DOIUrl":"https://doi.org/10.15227/orgsyn.098.0315","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":"1 1","pages":""},"PeriodicalIF":0.7,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67340821","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
Palladium-Catalyzed Hydrodefluorination of Fluoroarenes 钯催化氟芳烃的加氢脱氟
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2021-01-01 DOI: 10.15227/ORGSYN.098.0131
Joseph J. Gair
{"title":"Palladium-Catalyzed Hydrodefluorination of Fluoroarenes","authors":"Joseph J. Gair","doi":"10.15227/ORGSYN.098.0131","DOIUrl":"https://doi.org/10.15227/ORGSYN.098.0131","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":"98 1","pages":"131-146"},"PeriodicalIF":0.7,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67340269","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
Late-stage C-H Functionalization with 2,3,7,8–Tetrafluorothianthrene: Preparation of a Tetrafluorothianthrenium-salt 2,3,7,8 -四氟噻吩的后期C-H功能化:四氟噻吩盐的制备
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2021-01-01 DOI: 10.15227/orgsyn.098.0531
Samira Speicher
{"title":"Late-stage C-H Functionalization with 2,3,7,8–Tetrafluorothianthrene: Preparation of a Tetrafluorothianthrenium-salt","authors":"Samira Speicher","doi":"10.15227/orgsyn.098.0531","DOIUrl":"https://doi.org/10.15227/orgsyn.098.0531","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":"1 1","pages":""},"PeriodicalIF":0.7,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67340899","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
Synthesis of a Phosphorous Sulfur Incorporating Reagent for the Enantioselective Synthesis of Thiophosphates 对映选择性合成硫代磷酸盐用磷硫结合试剂的合成
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2021-01-01 DOI: 10.15227/orgsyn.098.0097
Prantik Maity
{"title":"Synthesis of a Phosphorous Sulfur Incorporating Reagent for the Enantioselective Synthesis of Thiophosphates","authors":"Prantik Maity","doi":"10.15227/orgsyn.098.0097","DOIUrl":"https://doi.org/10.15227/orgsyn.098.0097","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":"1 1","pages":""},"PeriodicalIF":0.7,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67340153","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
Catalytic Diazoalkane-Carbonyl Homologation: Synthesis of 2,2-Diphenylcycloheptanone and Other Quaternary or Tertiary Arylalkanones and Spirocycles by Ring Expansion 催化重氮烷烃-羰基同源化:扩环法合成2,2-二苯基环庚酮和其他季或叔芳烷酮及螺环
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2021-01-01 DOI: 10.15227/orgsyn.098.0343
Jason S. Kingsbury
{"title":"Catalytic Diazoalkane-Carbonyl Homologation: Synthesis of 2,2-Diphenylcycloheptanone and Other Quaternary or Tertiary Arylalkanones and Spirocycles by Ring Expansion","authors":"Jason S. Kingsbury","doi":"10.15227/orgsyn.098.0343","DOIUrl":"https://doi.org/10.15227/orgsyn.098.0343","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":"1 1","pages":""},"PeriodicalIF":0.7,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67340437","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 (S)-tert-ButylPyOx and Palladium-Catalyzed Asymmetric Conjugate Addition of Arylboronic Acids. 讨论附录:(S)-叔丁基pyox和钯催化芳香硼酸的不对称共轭加成的制备。
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2021-01-01 DOI: 10.15227/orgsyn.098.0117
Stephen R Sardini, Brian M Stoltz
{"title":"Discussion Addendum for: Preparation of (<i>S</i>)-<i>tert</i>-ButylPyOx and Palladium-Catalyzed Asymmetric Conjugate Addition of Arylboronic Acids.","authors":"Stephen R Sardini,&nbsp;Brian M Stoltz","doi":"10.15227/orgsyn.098.0117","DOIUrl":"https://doi.org/10.15227/orgsyn.098.0117","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":"98 ","pages":"117-130"},"PeriodicalIF":0.7,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9558615/pdf/nihms-1703820.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33517008","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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