首页 > 最新文献

Organic Syntheses最新文献

英文 中文
Chiral Organoiodine-catalyzed Enantioselective Oxidative Dearomatization of Phenols 手性有机碘催化苯酚的对映选择性氧化脱芳
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2021-01-01 DOI: 10.15227/ORGSYN.098.0028
M. Uyanik
{"title":"Chiral Organoiodine-catalyzed Enantioselective Oxidative Dearomatization of Phenols","authors":"M. Uyanik","doi":"10.15227/ORGSYN.098.0028","DOIUrl":"https://doi.org/10.15227/ORGSYN.098.0028","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":"98 1","pages":"28-50"},"PeriodicalIF":0.7,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67339990","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
Discussion Addendum for: Intra- and Intermolecular Kulinkovich Cyclopropanation Reactions of Carboxylic Esters with Olefins: Bicyclo[3.1.0]hexan-1-ol and trans-2-benzyl-1-methylcyclopropan-1-ol 讨论附录:羧酸酯与烯烃的分子内和分子间Kulinkovich环丙烷化反应:双环[3.1.0]己-1醇和反式2-苄基-1-甲基环丙烷-1醇
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2021-01-01 DOI: 10.15227/orgsyn.098.0430
J. Cha
{"title":"Discussion Addendum for: Intra- and Intermolecular Kulinkovich Cyclopropanation Reactions of Carboxylic Esters with Olefins: Bicyclo[3.1.0]hexan-1-ol and trans-2-benzyl-1-methylcyclopropan-1-ol","authors":"J. Cha","doi":"10.15227/orgsyn.098.0430","DOIUrl":"https://doi.org/10.15227/orgsyn.098.0430","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":"67340536","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 tert-Alkyl Phosphines: Preparation of Di-(1-adamantyl)phosphonium Trifluoromethanesulfonate and Tri-(1-adamantyl)phosphine 叔烷基膦的合成:三氟甲磺酸二(1-金刚烷基)磷和三(1-金刚烷基)膦的制备
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2021-01-01 DOI: 10.15227/orgsyn.098.0289
Thomas Barber
{"title":"Synthesis of tert-Alkyl Phosphines: Preparation of Di-(1-adamantyl)phosphonium Trifluoromethanesulfonate and Tri-(1-adamantyl)phosphine","authors":"Thomas Barber","doi":"10.15227/orgsyn.098.0289","DOIUrl":"https://doi.org/10.15227/orgsyn.098.0289","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":"67340688","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 2-(Triethylsilyl)cyclohex-1-en-1-yl Trifluoromethanesulfonate as a Precursor to Cyclohexyne 2-(三乙基硅基)环己基-1-烯-1-基三氟甲烷磺酸盐作为环己炔前驱体的制备
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2021-01-01 DOI: 10.15227/orgsyn.098.0509
Kazuki Inoue
{"title":"Preparation of 2-(Triethylsilyl)cyclohex-1-en-1-yl Trifluoromethanesulfonate as a Precursor to Cyclohexyne","authors":"Kazuki Inoue","doi":"10.15227/orgsyn.098.0509","DOIUrl":"https://doi.org/10.15227/orgsyn.098.0509","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":"67341333","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 and Acylation of 1,3-Thiazinane-2-thione 1,3-噻嗪-2-硫酮的合成与酰化
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2021-01-01 DOI: 10.15227/orgsyn.098.0374
S. Kennington
{"title":"Synthesis and Acylation of 1,3-Thiazinane-2-thione","authors":"S. Kennington","doi":"10.15227/orgsyn.098.0374","DOIUrl":"https://doi.org/10.15227/orgsyn.098.0374","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":"67340782","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
A nti ‐1,2,2,3,4,4‐Hexamethylphosphetane 1‐Oxide 反-1,2,2,3,4,4-六甲基膦-1-氧化物
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2020-04-29 DOI: 10.1002/0471264229.os096.26
Trevor V. Nykaza, J. Cooper, A. Radosevich, Robert-Cristian Raclea, Kyan A. D’Angelo, M. Movassaghi
{"title":"A\u0000 nti\u0000 ‐1,2,2,3,4,4‐Hexamethylphosphetane 1‐Oxide","authors":"Trevor V. Nykaza, J. Cooper, A. Radosevich, Robert-Cristian Raclea, Kyan A. D’Angelo, M. Movassaghi","doi":"10.1002/0471264229.os096.26","DOIUrl":"https://doi.org/10.1002/0471264229.os096.26","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":"1 1","pages":""},"PeriodicalIF":0.7,"publicationDate":"2020-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42797183","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: Phosphine‐Catalyzed [3 + 2] Annulation: Synthesis of Ethyl 5‐( tert ‐Butyl)‐2‐Phenyl‐1‐Tosyl‐3‐Pyrroline‐3‐Carboxylate 讨论附录:膦-催化[3 + 2]环化:乙基5 -(叔丁基)- 2 -苯基- 1 - Tosyl - 3 -吡咯啉- 3 -羧酸盐的合成
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2020-04-29 DOI: 10.1002/0471264229.OS096.14
Aslam C. Shaikh, Ohuyn Kwon
{"title":"Discussion Addendum for: Phosphine‐Catalyzed [3 + 2] Annulation: Synthesis of Ethyl 5‐(\u0000 tert\u0000 ‐Butyl)‐2‐Phenyl‐1‐Tosyl‐3‐Pyrroline‐3‐Carboxylate","authors":"Aslam C. Shaikh, Ohuyn Kwon","doi":"10.1002/0471264229.OS096.14","DOIUrl":"https://doi.org/10.1002/0471264229.OS096.14","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":"47387757","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 5‐Hydroxy‐4‐Methoxy‐2‐Methylpyrylium Trifluoromethanesulfonate from Kojic Acid 以曲酸为原料合成5-羟基-4-甲氧基-2-甲基吡啶基三氟甲磺酸酯
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2020-04-29 DOI: 10.1002/0471264229.os096.30
Nana B. Agyemang, Ryan P. Murelli, Richard K Jackson, J. Wood
{"title":"Synthesis of 5‐Hydroxy‐4‐Methoxy‐2‐Methylpyrylium Trifluoromethanesulfonate from Kojic Acid","authors":"Nana B. Agyemang, Ryan P. Murelli, Richard K Jackson, J. Wood","doi":"10.1002/0471264229.os096.30","DOIUrl":"https://doi.org/10.1002/0471264229.os096.30","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":"49483879","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: Fluorobis(phenylsulfonyl)methane ( FBSM ) 讨论增编:含氟(苯基磺酰)甲烷(FBSM)
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2020-04-29 DOI: 10.1002/0471264229.os096.29
Xanath Ispizua‐Rodriguez, V. Krishnamurti, M. Coe, G. Prakash
{"title":"Discussion Addendum for: Fluorobis(phenylsulfonyl)methane (\u0000 FBSM\u0000 )","authors":"Xanath Ispizua‐Rodriguez, V. Krishnamurti, M. Coe, G. Prakash","doi":"10.1002/0471264229.os096.29","DOIUrl":"https://doi.org/10.1002/0471264229.os096.29","url":null,"abstract":"","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":"1 1","pages":"1-20"},"PeriodicalIF":0.7,"publicationDate":"2020-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45221266","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 Highly Enantiomerically Enriched Amines by Asymmetric Transfer Hydrogenation of N‐ ( tert ‐Butylsulfinyl) Imines 讨论附录:N -(叔丁基亚胺基)亚胺不对称转移加氢合成高度对映体富集胺
IF 0.7 Q4 CHEMISTRY, ORGANIC
Organic Syntheses
Pub Date : 2020-04-29 DOI: 10.1002/0471264229.OS096.15
M. Yus
{"title":"Discussion Addendum For: Synthesis of Highly Enantiomerically Enriched Amines by Asymmetric Transfer Hydrogenation of\u0000 N‐\u0000 (\u0000 tert\u0000 ‐Butylsulfinyl) Imines","authors":"M. Yus","doi":"10.1002/0471264229.OS096.15","DOIUrl":"https://doi.org/10.1002/0471264229.OS096.15","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":"47581201","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
首页 上一页 下一页 尾页
类型
全部 化学•材料 生命科学 医学 物理 工程技术 环境•农林 材料科学 地球科学 法学 管理学 化学 环境科学与生态学 计算机科学 教育学 经济学 农林科学 人文科学 生物学 数学 物理与天体物理 心理学 综合性期刊 其他 工业工程 理学 历史学 农学 文学 信息工程
数据库
全部 ACS Publications Elsevier ieeexplore Springer The Royal Society of Chemistry Wiley
期刊
Organic Syntheses
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