Heterocycles : an international journal for reviews and communications in heterocyclic chemistry最新文献

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SYNTHESIS OF PHOTOREACTIVE DIAZIRINYL SALICIN DERIVATIVE TO ELUCIDATE FUNCTIONAL ANALYSIS OF THE BITTER TASTE RECEPTOR (Dedicated to Professor Isao Kuwajima on the occasion of his 77th birthday) 光反应性二氮基水杨苷衍生物的合成以阐明苦味受体的功能分析(在Kuwajima教授77岁生日之际献给他)
Munenori Sakurai, Takuma Yoshida, Lei Wang, Yuta Murai, K. Masuda, Y. Sakihama, Y. Hashidoko, Y. Hatanaka, M. Hashimoto
{"title":"SYNTHESIS OF PHOTOREACTIVE DIAZIRINYL SALICIN DERIVATIVE TO ELUCIDATE FUNCTIONAL ANALYSIS OF THE BITTER TASTE RECEPTOR (Dedicated to Professor Isao Kuwajima on the occasion of his 77th birthday)","authors":"Munenori Sakurai, Takuma Yoshida, Lei Wang, Yuta Murai, K. Masuda, Y. Sakihama, Y. Hashidoko, Y. Hatanaka, M. Hashimoto","doi":"10.3987/COM-14-S(K)36","DOIUrl":"https://doi.org/10.3987/COM-14-S(K)36","url":null,"abstract":"Salicin (salicyl alcohol glucoside) is a substance well known for its bitter taste. A photoreactive diazirinyl derivative of salicin will be utilized for the functional analysis of interactions between the bitter taste receptor and salicin. Glucosides of salicyl derivatives are more difficult than phenol derivatives that are unsubstituted at the ortho-position. A diazirinyl salicin derivative was synthesized at moderate yields by glucosidation of 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide and 2-hydroxy-4-[3-(trifluoromethyl)-3H-diazirin-3-yl]-benzaldehyde in the presence of a phase-transfer catalyst, nBuEt3NBr, followed by reduction and deprotection. Salicin is long known as one of the major components of phenyl glycosides in the family Salicaceae and is a bitter anti-inflammatory compound. Elucidation of the functions of its gustatory receptor on the basis of structure–activity relationships may reveal the mechanism of homeostatic functions, which is of great interest to scientists. Photoaffinity labeling is one of the most common techniques used in the analysis of chemical biology. To the best of our knowledge, there are no reports on the preparation of photoreactive salicin derivatives for the analysis of bitter taste receptors. Two modifications of phenyl glucoside derivatives using diazirine have been reported. The derivatives are not substituted at the o-position of phenol. One modification is glucosidation of p-diazirinyl phenol to synthesize α-glucoside and the other This paper is dedicated to Prof. Dr. Isao Kuwajima on the occasion of his 77th birthday. is construction of the diazirine moiety in the precursor of the phenyl glucoside derivative. However, glucosides of salicyl alcohol derivatives are more complicated than glucosides of the o-position unsubstituted phenol derivatives. Optimization of glucosidation of salicyl alcohol or salicyl aldehyde derivatives is essential to the synthesis of target diazirinyl derivatives of salicin. In this study, we report the synthesis of diazirinyl derivative and preliminary screening of glucosidations for salicyl alcohol and salicyl aldehyde derivatives. O OH HO HO OH O F3C N N OH O OAc AcO AcO AcO OAc F3C N N","PeriodicalId":12850,"journal":{"name":"Heterocycles : an international journal for reviews and communications in heterocyclic chemistry","volume":"66 1","pages":"698-705"},"PeriodicalIF":0.0,"publicationDate":"2015-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83378767","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: 4
INVESTIGATION OF Pd(II)-CATALYZED CYCLIZATION OF CHIRAL θ-HYDROXY-α,β,γ,δ-UNSATURATED DIENOL (Dedicated to Professor Isao Kuwajima on the occasion of his 77th birthday) Pd(II)催化手性θ-羟基-α,β,γ,δ-不饱和二烯醇环化反应的研究(在Kuwajima教授77岁生日之际献给他)
A. Ida, N. Hoshiya, J. Uenishi
{"title":"INVESTIGATION OF Pd(II)-CATALYZED CYCLIZATION OF CHIRAL θ-HYDROXY-α,β,γ,δ-UNSATURATED DIENOL (Dedicated to Professor Isao Kuwajima on the occasion of his 77th birthday)","authors":"A. Ida, N. Hoshiya, J. Uenishi","doi":"10.3987/COM-14-S(K)77","DOIUrl":"https://doi.org/10.3987/COM-14-S(K)77","url":null,"abstract":"","PeriodicalId":12850,"journal":{"name":"Heterocycles : an international journal for reviews and communications in heterocyclic chemistry","volume":"42 1","pages":"1082-1093"},"PeriodicalIF":0.0,"publicationDate":"2015-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78841370","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
DESIGN OF AZA-POLYQUINANES VIA FISCHER INDOLE CYCLIZATION UNDER GREEN CONDITIONS (Dedicated to Professor Isao Kuwajima on the occasion of his 77th birthday) 绿色条件下通过FISCHER吲哚环化设计aza -聚醌(在Kuwajima教授77岁生日之际献给他)
S. Kotha, A. Chinnam
{"title":"DESIGN OF AZA-POLYQUINANES VIA FISCHER INDOLE CYCLIZATION UNDER GREEN CONDITIONS (Dedicated to Professor Isao Kuwajima on the occasion of his 77th birthday)","authors":"S. Kotha, A. Chinnam","doi":"10.3987/COM-14-S(K)35","DOIUrl":"https://doi.org/10.3987/COM-14-S(K)35","url":null,"abstract":"","PeriodicalId":12850,"journal":{"name":"Heterocycles : an international journal for reviews and communications in heterocyclic chemistry","volume":"76 1","pages":"690-697"},"PeriodicalIF":0.0,"publicationDate":"2015-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86714534","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
Pd-CATALYZED INTRAMOLECULAR OXIDATIVE COUPLING REACTION OF 1,1'-CARBONYLDIINDOLES (Dedicated to Professor Isao Kuwajima on the occasion of his 77th birthday) pd催化的1,1′-羰基二吲哚分子内氧化偶联反应(在Kuwajima教授77岁生日之际献给他)
Takumi Abe, M. Ishikura
{"title":"Pd-CATALYZED INTRAMOLECULAR OXIDATIVE COUPLING REACTION OF 1,1'-CARBONYLDIINDOLES (Dedicated to Professor Isao Kuwajima on the occasion of his 77th birthday)","authors":"Takumi Abe, M. Ishikura","doi":"10.3987/COM-14-S(K)28","DOIUrl":"https://doi.org/10.3987/COM-14-S(K)28","url":null,"abstract":"","PeriodicalId":12850,"journal":{"name":"Heterocycles : an international journal for reviews and communications in heterocyclic chemistry","volume":"75 1","pages":"673-680"},"PeriodicalIF":0.0,"publicationDate":"2015-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86104232","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
A NEW CLASS OF STRUCTURALLY SIMPLE AND HIGHLY EMISSIVE FLUOROPHORES WITH A PYRIDINE–ACETYLENE–PHENOL CONJUGATE (Dedicated to Professor Isao Kuwajima on the occasion of his 77th birthday) 一类结构简单、高发射的新型吡啶-乙炔-苯酚偶联物荧光团(在Kuwajima教授77岁生日之际献给他)
Yuki Ohishi, H. Abe, M. Inouye
{"title":"A NEW CLASS OF STRUCTURALLY SIMPLE AND HIGHLY EMISSIVE FLUOROPHORES WITH A PYRIDINE–ACETYLENE–PHENOL CONJUGATE (Dedicated to Professor Isao Kuwajima on the occasion of his 77th birthday)","authors":"Yuki Ohishi, H. Abe, M. Inouye","doi":"10.3987/COM-14-S(K)51","DOIUrl":"https://doi.org/10.3987/COM-14-S(K)51","url":null,"abstract":"","PeriodicalId":12850,"journal":{"name":"Heterocycles : an international journal for reviews and communications in heterocyclic chemistry","volume":"42 1","pages":"515-528"},"PeriodicalIF":0.0,"publicationDate":"2015-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90750284","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: 4
SIMPLE SYNTHETIC METHOD FOR 1-HYDROXYINDOLE AND ITS APPLICATION TO 1-HYDROXYTRYPTOPHAN DERIVATIVES (Dedicated to Professor Isao Kuwajima on the occasion of his 77th birthday) 1-羟基吲哚的简单合成方法及其在1-羟基色氨酸衍生物中的应用(在Kuwajima教授77岁生日之际献给他)
T. Kawasaki, M. Tabata, K. Nakagawa
{"title":"SIMPLE SYNTHETIC METHOD FOR 1-HYDROXYINDOLE AND ITS APPLICATION TO 1-HYDROXYTRYPTOPHAN DERIVATIVES (Dedicated to Professor Isao Kuwajima on the occasion of his 77th birthday)","authors":"T. Kawasaki, M. Tabata, K. Nakagawa","doi":"10.3987/COM-14-S(K)74","DOIUrl":"https://doi.org/10.3987/COM-14-S(K)74","url":null,"abstract":"","PeriodicalId":12850,"journal":{"name":"Heterocycles : an international journal for reviews and communications in heterocyclic chemistry","volume":"1 1","pages":"1038-1071"},"PeriodicalIF":0.0,"publicationDate":"2015-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82262990","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: 4
REDOX RESPONSIVE POLYMER INCORPORATED WITH MESOGENIC UNIT AND BIS(BENZODITHIOLYL)BITHIENYL SCAFFOLD (Dedicated to Professor Isao Kuwajima on the occasion of his 77th birthday) 含介源单元和BIS(苯并二硫酰基)二硫基支架的氧化还原反应聚合物(在Kuwajima教授77岁生日之际献给他)
T. Ohtake, Hideki Tanaka, Tetsuro Matsumoto
{"title":"REDOX RESPONSIVE POLYMER INCORPORATED WITH MESOGENIC UNIT AND BIS(BENZODITHIOLYL)BITHIENYL SCAFFOLD (Dedicated to Professor Isao Kuwajima on the occasion of his 77th birthday)","authors":"T. Ohtake, Hideki Tanaka, Tetsuro Matsumoto","doi":"10.3987/COM-14-S(K)44","DOIUrl":"https://doi.org/10.3987/COM-14-S(K)44","url":null,"abstract":"","PeriodicalId":12850,"journal":{"name":"Heterocycles : an international journal for reviews and communications in heterocyclic chemistry","volume":"14 1","pages":"811-818"},"PeriodicalIF":0.0,"publicationDate":"2015-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82403578","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
FORMATION OF 2-ACETAMIDO-2-DEOXY-D-GLUCOPYRANOSIDIC LINKAGES VIA GLYCOSIDATION USING A COMBINATION OF TWO LEWIS ACIDS (Dedicated to Professor Isao Kuwajima on the occasion of his 77th birthday) 利用两种LEWIS酸的组合通过糖苷化形成2-乙酰氨基-2-脱氧- d -葡萄糖吡喃苷键(在Kuwajima教授77岁生日之际献给他)
Yoshiki Oda, M. Midorikawa, T. Yamanoi
{"title":"FORMATION OF 2-ACETAMIDO-2-DEOXY-D-GLUCOPYRANOSIDIC LINKAGES VIA GLYCOSIDATION USING A COMBINATION OF TWO LEWIS ACIDS (Dedicated to Professor Isao Kuwajima on the occasion of his 77th birthday)","authors":"Yoshiki Oda, M. Midorikawa, T. Yamanoi","doi":"10.3987/COM-14-S(K)4","DOIUrl":"https://doi.org/10.3987/COM-14-S(K)4","url":null,"abstract":"","PeriodicalId":12850,"journal":{"name":"Heterocycles : an international journal for reviews and communications in heterocyclic chemistry","volume":"25 1","pages":"198-215"},"PeriodicalIF":0.0,"publicationDate":"2015-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82910857","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
Mn(III)-BASED OXIDATIVE CYCLIZATION OF N-ARYL-3-OXOBUTANAMIDES. FACILE SYNTHESIS AND TRANSFORMATION OF SUBSTITUTED OXINDOLES (Dedicated to Professor Isao Kuwajima on the occasion of his 77th birthday) n -芳基-3-氧丁烷酰胺的Mn(III)基氧化环化。取代吲哚的快速合成和转化(在Kuwajima教授77岁生日之际致辞)
Nobutaka Kikue, Tetsuya Takahashi, H. Nishino
{"title":"Mn(III)-BASED OXIDATIVE CYCLIZATION OF N-ARYL-3-OXOBUTANAMIDES. FACILE SYNTHESIS AND TRANSFORMATION OF SUBSTITUTED OXINDOLES (Dedicated to Professor Isao Kuwajima on the occasion of his 77th birthday)","authors":"Nobutaka Kikue, Tetsuya Takahashi, H. Nishino","doi":"10.3987/COM-14-S(K)57","DOIUrl":"https://doi.org/10.3987/COM-14-S(K)57","url":null,"abstract":"The oxidation of 3-oxo-N-phenylbutanamides 1 with manganese(III) acetate in ethanol afforded dimeric 3,3'-biindoline-2,2'-dione derivatives 3–5. A similar reaction of N,2-disubstituted N-aryl-3-oxobutanamides 6 in acetic acid produced 3-acetylindolin-2-ones 7 bearing various substituents in good to excellent yields. The acetylindolinones 7 were easily deacetylated by treatment using neutral alumina in diethyl ether. Both the acetylindolinones 7 and deacetylated indolinones 8 were transformed by reduction into the substituted 1H-indoles. INTRODUCTION Many of the chemistries for indoles and their derivatives have been investigated and reported. However, the synthesis and reaction of these heterocycles are still attractive from the view point of the synthetic method, total synthesis of natural products, biological and pharmacological activities, and material science. Recently, we reported the Mn(III)-mediated direct substitution of methoxynaphthalenes with N-aryl-3-oxobutanamides, giving the 3-oxobutanamide-substituted naphthalene I in addition to a small amount of demethoxylated naphthofuran II and benzoindolinone III (Scheme 1, eq. 1). Although the yield of the heterocyclic compounds II and III was poor, the carbon-carbon bond formation efficiently occurred during the reaction. We also reported the facile synthesis of 3,4-dihydro-2(1H)-quinolinones, 540 HETEROCYCLES, Vol. 90, No. 1, 2015","PeriodicalId":12850,"journal":{"name":"Heterocycles : an international journal for reviews and communications in heterocyclic chemistry","volume":"41 1","pages":"540-562"},"PeriodicalIF":0.0,"publicationDate":"2015-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76829134","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: 16
SYNTHESIS OF RHODOTORULIC ACID AND ITS 1,4-DIMETHYLATED DERIVATIVE (Dedicated to Professor Isao Kuwajima on the occasion of his 77th birthday) RHODOTORULIC酸及其1,4-二甲基化衍生物的合成(在Kuwajima教授77岁生日之际献给他)
Michiyasu Nakao, Shintaro Fukayama, Syuji Kitaike
{"title":"SYNTHESIS OF RHODOTORULIC ACID AND ITS 1,4-DIMETHYLATED DERIVATIVE (Dedicated to Professor Isao Kuwajima on the occasion of his 77th birthday)","authors":"Michiyasu Nakao, Shintaro Fukayama, Syuji Kitaike","doi":"10.3987/COM-14-S(K)67","DOIUrl":"https://doi.org/10.3987/COM-14-S(K)67","url":null,"abstract":"","PeriodicalId":12850,"journal":{"name":"Heterocycles : an international journal for reviews and communications in heterocyclic chemistry","volume":"39 1","pages":"1309-1316"},"PeriodicalIF":0.0,"publicationDate":"2015-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82703120","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
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