首页 > 最新文献

ChemInform最新文献

英文 中文
ChemInform Abstract: Ruthenium-Catalyzed Direct N-Alkylation of Amines with Carboxylic Acids Using Methylphenylsilane as a Hydride Source. 摘要钌催化以甲基苯基硅烷为氢化物源的胺与羧酸直接n -烷基化反应。
ChemInform
Pub Date : 2016-12-06 DOI: 10.1002/chin.201652075
Maki Minakawa, Masataka Okubo, Motoi Kawatsura

The novel reaction conditions allow the direct mono-N-alkylation of primary aromatic amines.

新的反应条件允许伯胺的直接单n烷基化。
{"title":"ChemInform Abstract: Ruthenium-Catalyzed Direct N-Alkylation of Amines with Carboxylic Acids Using Methylphenylsilane as a Hydride Source.","authors":"Maki Minakawa,&nbsp;Masataka Okubo,&nbsp;Motoi Kawatsura","doi":"10.1002/chin.201652075","DOIUrl":"10.1002/chin.201652075","url":null,"abstract":"<p>The novel reaction conditions allow the direct mono-N-alkylation of primary aromatic amines.</p>","PeriodicalId":9834,"journal":{"name":"ChemInform","volume":"47 52","pages":""},"PeriodicalIF":0.0,"publicationDate":"2016-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/chin.201652075","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77029110","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
ChemInform Abstract: Copper-Mediated Etherification of Arenes with Alkoxysilanes Directed by an (2-Aminophenyl)pyrazole Group. 摘要/ Abstract摘要:铜介导的(2-氨基苯基)吡唑基芳烃与烷氧基硅烷醚化反应。
ChemInform
Pub Date : 2016-12-06 DOI: 10.1002/chin.201652130
Jayaraman Selvakumar, Gowri Sankar Grandhi, Harekrishna Sahoo, Mahiuddin Baidya
{"title":"ChemInform Abstract: Copper-Mediated Etherification of Arenes with Alkoxysilanes Directed by an (2-Aminophenyl)pyrazole Group.","authors":"Jayaraman Selvakumar,&nbsp;Gowri Sankar Grandhi,&nbsp;Harekrishna Sahoo,&nbsp;Mahiuddin Baidya","doi":"10.1002/chin.201652130","DOIUrl":"10.1002/chin.201652130","url":null,"abstract":"","PeriodicalId":9834,"journal":{"name":"ChemInform","volume":"47 52","pages":""},"PeriodicalIF":0.0,"publicationDate":"2016-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/chin.201652130","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82477284","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
ChemInform Abstract: Palladium-Catalyzed Suzuki—Miyaura Reaction of Fluorinated Vinyl Chloride: A New Approach for Synthesis α- and α,β-Trifluoromethylstyrenes. 摘要:钯催化的氟化氯乙烯Suzuki-Miyaura反应:合成α-和α，β-三氟甲基苯乙烯的新方法。
ChemInform
Pub Date : 2016-12-06 DOI: 10.1002/chin.201652118
Yang Li, Bo Zhao, Kun Dai, Dong-Huai Tu, Bo Wang, Yao-Yu Wang, Zhao-Tie Liu, Zhong-Wen Liu, Jian Lu

Optimized conditions including the phosphine ligand (PPC) allow the efficient synthesis of trifluoromethylstyrenes from fluorinated vinyl chlorides and arylboronic acids.

包括膦配体(PPC)在内的优化条件允许从氟化氯乙烯和芳基硼酸中高效合成三氟甲基苯乙烯。
{"title":"ChemInform Abstract: Palladium-Catalyzed Suzuki—Miyaura Reaction of Fluorinated Vinyl Chloride: A New Approach for Synthesis α- and α,β-Trifluoromethylstyrenes.","authors":"Yang Li,&nbsp;Bo Zhao,&nbsp;Kun Dai,&nbsp;Dong-Huai Tu,&nbsp;Bo Wang,&nbsp;Yao-Yu Wang,&nbsp;Zhao-Tie Liu,&nbsp;Zhong-Wen Liu,&nbsp;Jian Lu","doi":"10.1002/chin.201652118","DOIUrl":"10.1002/chin.201652118","url":null,"abstract":"<p>Optimized conditions including the phosphine ligand (PPC) allow the efficient synthesis of trifluoromethylstyrenes from fluorinated vinyl chlorides and arylboronic acids.</p>","PeriodicalId":9834,"journal":{"name":"ChemInform","volume":"47 52","pages":""},"PeriodicalIF":0.0,"publicationDate":"2016-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/chin.201652118","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81331854","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: 8
ChemInform Abstract: Catalyst-Free Synthesis of 2-(tert-Butyldisulfanyl) Heterocycles from tert-Butanesulfinamide and Mercapto-Substituted Imidazoles, Tetrazole, Pyrimidine and Pyridine. 摘要:叔丁烷磺酰胺与巯基取代咪唑、四唑、嘧啶和吡啶无催化剂合成2-(叔丁基二磺胺基)杂环化合物。
ChemInform
Pub Date : 2016-12-06 DOI: 10.1002/chin.201652185
Yue Zhou, Xingzhao Tu, Zhijie Li, Lihong Zhou, Qingle Zeng
{"title":"ChemInform Abstract: Catalyst-Free Synthesis of 2-(tert-Butyldisulfanyl) Heterocycles from tert-Butanesulfinamide and Mercapto-Substituted Imidazoles, Tetrazole, Pyrimidine and Pyridine.","authors":"Yue Zhou,&nbsp;Xingzhao Tu,&nbsp;Zhijie Li,&nbsp;Lihong Zhou,&nbsp;Qingle Zeng","doi":"10.1002/chin.201652185","DOIUrl":"10.1002/chin.201652185","url":null,"abstract":"","PeriodicalId":9834,"journal":{"name":"ChemInform","volume":"47 52","pages":""},"PeriodicalIF":0.0,"publicationDate":"2016-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/chin.201652185","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82239105","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
ChemInform Abstract: Chemo- and Regio-Selective Synthesis of Hexacyclic Indeno-Fused Coumarins via Domino Diels—Alder Dimerization/Baeyer—Villiger Oxidation. 摘要/ Abstract摘要:采用Domino Diels-Alder二聚化/ Baeyer-Villiger氧化法制备六环芳香融合香豆素。
ChemInform
Pub Date : 2016-12-06 DOI: 10.1002/chin.201652036
Tanmoy Chanda, Sushobhan Chowdhury, Suvajit Koley, Maya Shankar Singh

Two parallel chemoselective synthetic transformations using substituted indenones as a synthon in Diels—Alder reactions is reported.

报道了在Diels-Alder反应中以取代茚酮为合子的两种平行化学选择性合成转化。
{"title":"ChemInform Abstract: Chemo- and Regio-Selective Synthesis of Hexacyclic Indeno-Fused Coumarins via Domino Diels—Alder Dimerization/Baeyer—Villiger Oxidation.","authors":"Tanmoy Chanda,&nbsp;Sushobhan Chowdhury,&nbsp;Suvajit Koley,&nbsp;Maya Shankar Singh","doi":"10.1002/chin.201652036","DOIUrl":"10.1002/chin.201652036","url":null,"abstract":"<p>Two parallel chemoselective synthetic transformations using substituted indenones as a synthon in Diels—Alder reactions is reported.</p>","PeriodicalId":9834,"journal":{"name":"ChemInform","volume":"47 52","pages":""},"PeriodicalIF":0.0,"publicationDate":"2016-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/chin.201652036","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82333446","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
ChemInform Abstract: Recent Advancement of Ullmann-Type Coupling Reactions in the Formation of C—C Bond 摘要:C-C键形成中的ullmann型偶联反应研究进展
ChemInform
Pub Date : 2016-12-06 DOI: 10.1002/chin.201652496
Shovan Mondal

Review: 64 refs.

综述:64篇参考文献。
{"title":"ChemInform Abstract: Recent Advancement of Ullmann-Type Coupling Reactions in the Formation of C—C Bond","authors":"Shovan Mondal","doi":"10.1002/chin.201652496","DOIUrl":"10.1002/chin.201652496","url":null,"abstract":"<p>Review: 64 refs.</p>","PeriodicalId":9834,"journal":{"name":"ChemInform","volume":"47 52","pages":""},"PeriodicalIF":0.0,"publicationDate":"2016-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/chin.201652496","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82471076","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
ChemInform Abstract: FeCl3-Catalyzed Ring-Closing Carbonyl—Olefin Metathesis. 摘要:fecl3催化闭合环羰基烯烃复分解。
ChemInform
Pub Date : 2016-12-06 DOI: 10.1002/chin.201652055
Lina Ma, Wenjuan Li, Hui Xi, Xiaohui Bai, Enlu Ma, Xiaoyu Yan, Zhiping Li
{"title":"ChemInform Abstract: FeCl3-Catalyzed Ring-Closing Carbonyl—Olefin Metathesis.","authors":"Lina Ma,&nbsp;Wenjuan Li,&nbsp;Hui Xi,&nbsp;Xiaohui Bai,&nbsp;Enlu Ma,&nbsp;Xiaoyu Yan,&nbsp;Zhiping Li","doi":"10.1002/chin.201652055","DOIUrl":"10.1002/chin.201652055","url":null,"abstract":"","PeriodicalId":9834,"journal":{"name":"ChemInform","volume":"47 52","pages":""},"PeriodicalIF":0.0,"publicationDate":"2016-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/chin.201652055","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87060049","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: 3
ChemInform Abstract: Electrophile-Induced Cyclization of 3-Alkynyl-2-arylquinoxalines: A Method for Benzo- and Naphthophenazine Synthesis. 摘要:亲电诱导3-炔基-2-芳基喹啉环化:一种苯并和萘吩嗪的合成方法。
ChemInform
Pub Date : 2016-12-06 DOI: 10.1002/chin.201652350
Anna V. Gulveskaya

A facile synthesis of benzo[a]-, naphtho[1,2-a]- and naphtho[2,1-a]phenazines by ICl-promoted 6-endo-dig cyclization of 3-alkynyl-2-arylquinoxalines is developed.

采用icl催化3-炔基-2-芳基喹啉6-内环合成了苯并[A]-、萘[1,2- A]-和萘[2,1- A]非那嗪。
{"title":"ChemInform Abstract: Electrophile-Induced Cyclization of 3-Alkynyl-2-arylquinoxalines: A Method for Benzo- and Naphthophenazine Synthesis.","authors":"Anna V. Gulveskaya","doi":"10.1002/chin.201652350","DOIUrl":"10.1002/chin.201652350","url":null,"abstract":"<p>A facile synthesis of benzo[a]-, naphtho[1,2-a]- and naphtho[2,1-a]phenazines by ICl-promoted 6-endo-dig cyclization of 3-alkynyl-2-arylquinoxalines is developed.</p>","PeriodicalId":9834,"journal":{"name":"ChemInform","volume":"47 52","pages":""},"PeriodicalIF":0.0,"publicationDate":"2016-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/chin.201652350","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82643820","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
ChemInform Abstract: Fluorinated Diazoalkanes — A Versatile Class of Reagents for the Synthesis of Fluorinated Compounds 摘要:氟化重氮烷烃——一类合成氟化化合物的通用试剂
ChemInform
Pub Date : 2016-12-06 DOI: 10.1002/chin.201652474
Lucas Mertens, Rene M. Koenigs

Review: 79 refs.

回顾:79篇参考文献。
{"title":"ChemInform Abstract: Fluorinated Diazoalkanes — A Versatile Class of Reagents for the Synthesis of Fluorinated Compounds","authors":"Lucas Mertens,&nbsp;Rene M. Koenigs","doi":"10.1002/chin.201652474","DOIUrl":"10.1002/chin.201652474","url":null,"abstract":"<p>Review: 79 refs.</p>","PeriodicalId":9834,"journal":{"name":"ChemInform","volume":"47 52","pages":""},"PeriodicalIF":0.0,"publicationDate":"2016-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/chin.201652474","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89001121","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
ChemInform Abstract: Facile Synthesis of Naphtho[2,3-d]thiazoles, Naphtho[2,3-e][1,3,4]thiadiazines and Bis(naphtho[2,3-d]thiazolyl)copper(II) Derivatives from Heteroylthiosemicarbazides. 摘要:杂基硫代氨基脲类化合物催化合成萘[2,3-d]噻唑、萘[2,3-e][1,3,4]噻嗪和双(萘[2,3-d]噻唑基)铜(II)衍生物。
ChemInform
Pub Date : 2016-12-06 DOI: 10.1002/chin.201652058
Alaa A. Hassan, Nasr K. Mohamed, Lamiaa E. Abd El-Haleem, Stefan Braese, Martin Nieger
{"title":"ChemInform Abstract: Facile Synthesis of Naphtho[2,3-d]thiazoles, Naphtho[2,3-e][1,3,4]thiadiazines and Bis(naphtho[2,3-d]thiazolyl)copper(II) Derivatives from Heteroylthiosemicarbazides.","authors":"Alaa A. Hassan,&nbsp;Nasr K. Mohamed,&nbsp;Lamiaa E. Abd El-Haleem,&nbsp;Stefan Braese,&nbsp;Martin Nieger","doi":"10.1002/chin.201652058","DOIUrl":"10.1002/chin.201652058","url":null,"abstract":"","PeriodicalId":9834,"journal":{"name":"ChemInform","volume":"47 52","pages":""},"PeriodicalIF":0.0,"publicationDate":"2016-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/chin.201652058","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88093341","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
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
ChemInform
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