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ChemInform Abstract: Isolation of Lingzhifuran A and Lingzhilactones D—F from Ganoderma lucidum as Specific Smad3 Phosphorylation Inhibitors and Total Synthesis of Lingzhifuran A. 摘要:灵芝呋喃A和灵芝内酯D-F作为Smad3特异性磷酸化抑制剂的分离及灵芝呋喃A的全合成。
ChemInform Pub Date : 2016-12-06 DOI: 10.1002/chin.201652385
Wei-Yi Ding, Jun Ai, Xin-Long Wang, Fayang G. Qiu, Qing Lv, Ping Fang, Fan-Fan Hou, Yong-Ming Yan, Yong-Xian Cheng
{"title":"ChemInform Abstract: Isolation of Lingzhifuran A and Lingzhilactones D—F from Ganoderma lucidum as Specific Smad3 Phosphorylation Inhibitors and Total Synthesis of Lingzhifuran A.","authors":"Wei-Yi Ding,&nbsp;Jun Ai,&nbsp;Xin-Long Wang,&nbsp;Fayang G. Qiu,&nbsp;Qing Lv,&nbsp;Ping Fang,&nbsp;Fan-Fan Hou,&nbsp;Yong-Ming Yan,&nbsp;Yong-Xian Cheng","doi":"10.1002/chin.201652385","DOIUrl":"10.1002/chin.201652385","url":null,"abstract":"<p>The four new phenolic meroterpenoids, lingzhifuran A (I) and lingzhilactones D—F (II—IV), show inhibitory activities against transforming growth factor-β1-induced Smad3 phosphorylation.</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.201652385","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74838220","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: Increasing the Impact of Materials in and Beyond Bio-Nano Science 增加材料在生物纳米科学内外的影响
ChemInform Pub Date : 2016-12-06 DOI: 10.1002/chin.201652501
Mattias Bjoernmalm, Matthew Faria, Frank Caruso
{"title":"ChemInform Abstract: Increasing the Impact of Materials in and Beyond Bio-Nano Science","authors":"Mattias Bjoernmalm,&nbsp;Matthew Faria,&nbsp;Frank Caruso","doi":"10.1002/chin.201652501","DOIUrl":"10.1002/chin.201652501","url":null,"abstract":"<p>Review: 130 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.201652501","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72659457","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: 7
ChemInform Abstract: Novel One-Pot Synthesis of Symmetrically Substituted Ureas. 摘要:一锅法合成对称取代脲的新方法。
ChemInform Pub Date : 2016-12-06 DOI: 10.1002/chin.201652166
Xingxing Wu, Qingfen Niu, Tianduo Li
{"title":"ChemInform Abstract: Novel One-Pot Synthesis of Symmetrically Substituted Ureas.","authors":"Xingxing Wu,&nbsp;Qingfen Niu,&nbsp;Tianduo Li","doi":"10.1002/chin.201652166","DOIUrl":"10.1002/chin.201652166","url":null,"abstract":"<p>The simple and environmentally friendly protocol proceeds with inexpensive reagents.</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.201652166","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81939003","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: Clindanones A and B and Cladosporols F and G, Polyketides from the Deep-Sea Derived Fungus Cladosporium cladosporioides HDN14-342. 摘要:深海衍生真菌Cladosporium cladosporioides HDN14-342的Clindanones A、B和cladsporols F、G多酮类化合物。
ChemInform Pub Date : 2016-12-06 DOI: 10.1002/chin.201652419
Zhenzhen Zhang, Xueqian He, Congcong Liu, Qian Che, Tianjiao Zhu, Qianqun Gu, Dehai Li
{"title":"ChemInform Abstract: Clindanones A and B and Cladosporols F and G, Polyketides from the Deep-Sea Derived Fungus Cladosporium cladosporioides HDN14-342.","authors":"Zhenzhen Zhang,&nbsp;Xueqian He,&nbsp;Congcong Liu,&nbsp;Qian Che,&nbsp;Tianjiao Zhu,&nbsp;Qianqun Gu,&nbsp;Dehai Li","doi":"10.1002/chin.201652419","DOIUrl":"10.1002/chin.201652419","url":null,"abstract":"<p>Cladosporol G (I), together with another three new tetralone derivatives and three known biogenetically related polyketides, is isolated from title deep-sea derived fungus and is shown to have the best cytotoxic activity against HeLa cells with an IC<sub>50</sub> value of 3.9 μM.</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.201652419","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85911405","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: Synthesis of (1H-Pyrrol-1-yl)anthracene-9,10-diones. 摘要:(1h -吡咯-1-基)蒽-9,10-二酮的合成。
ChemInform Pub Date : 2016-12-06 DOI: 10.1002/chin.201652217
Viktor I. Zvarych, Maryna V. Stasevych, Volodymyr V. Lunin, Mykhailo V. Vovk, Volodymyr P. Novikov
{"title":"ChemInform Abstract: Synthesis of (1H-Pyrrol-1-yl)anthracene-9,10-diones.","authors":"Viktor I. Zvarych,&nbsp;Maryna V. Stasevych,&nbsp;Volodymyr V. Lunin,&nbsp;Mykhailo V. Vovk,&nbsp;Volodymyr P. Novikov","doi":"10.1002/chin.201652217","DOIUrl":"10.1002/chin.201652217","url":null,"abstract":"<p>The title compounds are prepared from (amino)anthracenediones and (dimethoxy)tetrahydrofuran via Clauson—Kaas reaction using I<sub>2</sub> as catalyst.</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.201652217","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76872294","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
ChemInform Abstract: Few-Layer Antimonene by Liquid-Phase Exfoliation. 摘要:液相剥离法制备少层锑烯。
ChemInform Pub Date : 2016-12-06 DOI: 10.1002/chin.201652019
Gonzalo Abellan,  et al.
{"title":"ChemInform Abstract: Few-Layer Antimonene by Liquid-Phase Exfoliation.","authors":"Gonzalo Abellan,&nbsp; et al.","doi":"10.1002/chin.201652019","DOIUrl":"10.1002/chin.201652019","url":null,"abstract":"<p>Highly stable iPrOH/H<sub>2</sub>O (4:1) suspensions of few-layer antimonene (FL-Sb) are prepared by liquid-phase exfoliation of ground Sb crystals via sonication without the need for surfactants (400 W, 24 kHz, 40 min).</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.201652019","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81249564","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: 5
ChemInform Abstract: The First Solvent-Free Synthesis of Privileged γ- and δ-Lactams via the Castagnoli—Cushman Reaction. 摘要:首次利用Castagnoli-Cushman反应无溶剂合成γ-和δ-内酰胺类化合物。
ChemInform Pub Date : 2016-12-06 DOI: 10.1002/chin.201652301
Anastasia Lepikhina, Olga Bakulina, Dmitry Dar'in, Mikhail Krasavin
{"title":"ChemInform Abstract: The First Solvent-Free Synthesis of Privileged γ- and δ-Lactams via the Castagnoli—Cushman Reaction.","authors":"Anastasia Lepikhina,&nbsp;Olga Bakulina,&nbsp;Dmitry Dar'in,&nbsp;Mikhail Krasavin","doi":"10.1002/chin.201652301","DOIUrl":"10.1002/chin.201652301","url":null,"abstract":"<p>36 examples</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.201652301","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84101199","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
ChemInform Abstract: Visible-Light Photoredox-Catalyzed Coupling Reaction of Azoles with α-Carbamoyl Sulfides. 摘要:可见光光氧化催化氮唑与α-氨基甲酰硫化物的偶联反应。
ChemInform Pub Date : 2016-12-06 DOI: 10.1002/chin.201652260
Lucie Jarrige, Guillaume Levitre, Geraldine Masson
{"title":"ChemInform Abstract: Visible-Light Photoredox-Catalyzed Coupling Reaction of Azoles with α-Carbamoyl Sulfides.","authors":"Lucie Jarrige,&nbsp;Guillaume Levitre,&nbsp;Geraldine Masson","doi":"10.1002/chin.201652260","DOIUrl":"10.1002/chin.201652260","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.201652260","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78344759","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: Simple Primary Amino Amide Organocatalyst for Enantioselective Aldol Reactions of Isatins with Ketones. 摘要:鸢尾素与酮类对映选择性醛醇反应的简单一级氨基酰胺有机催化剂。
ChemInform Pub Date : 2016-12-06 DOI: 10.1002/chin.201652223
Eunsang Kwon,  et al.
{"title":"ChemInform Abstract: Simple Primary Amino Amide Organocatalyst for Enantioselective Aldol Reactions of Isatins with Ketones.","authors":"Eunsang Kwon,&nbsp; et al.","doi":"10.1002/chin.201652223","DOIUrl":"10.1002/chin.201652223","url":null,"abstract":"<p>Among a number of amino acid amide-derived organocatalysts, L-tert-leucine derivative TLA features best efficiency in terms of yield, dia- and enantiostereoselectivities in the title reaction, in particular, when 6-membered saturated (hetero)cyclic ketones are used.</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.201652223","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77775502","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: Indoline-Based Constrained Peptidomimetic Motifs Obtained via the Joullie—Ugi Reaction of Indolenines. 摘要:通过吲哚啉的Joullie-Ugi反应获得了基于吲哚啉的受限拟肽基序。
ChemInform Pub Date : 2016-12-06 DOI: 10.1002/chin.201652222
Pavel Golubev, Olga Bakulina, Dmitry Dar'in, Mikhail Krasavin
{"title":"ChemInform Abstract: Indoline-Based Constrained Peptidomimetic Motifs Obtained via the Joullie—Ugi Reaction of Indolenines.","authors":"Pavel Golubev,&nbsp;Olga Bakulina,&nbsp;Dmitry Dar'in,&nbsp;Mikhail Krasavin","doi":"10.1002/chin.201652222","DOIUrl":"10.1002/chin.201652222","url":null,"abstract":"<p>Sterically demanding indolenines are employed as cyclic imine substrates in the title reaction with isocyanides and carboxylic acids, resulting in a new type of conformationally constrained indoline-based peptidomimetics.</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.201652222","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76758600","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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