发布求助
文献互助 智能选刊 最新文献

Organic Chemistry International最新文献

筛选
英文 中文
Stereoselective Synthesis of (+)-α-Conhydrine from R-(+)-Glyceraldehyde R-(+)-甘油醛立体选择性合成(+)-α- conhydrine
Organic Chemistry International Pub Date : 2014-10-20 DOI: 10.1155/2014/982716
Nageshwar Rao Penumati, Nagaiah Kommu
{"title":"Stereoselective Synthesis of (+)-α-Conhydrine from R-(+)-Glyceraldehyde","authors":"Nageshwar Rao Penumati, Nagaiah Kommu","doi":"10.1155/2014/982716","DOIUrl":"https://doi.org/10.1155/2014/982716","url":null,"abstract":"Stereoselective synthesis of (+)-α-Conhydrine was accomplished from protected (R)-(+)-glyceraldehyde, a familiar carbohydrate predecessor. Our synthetic strategy featured the following two key reactions. One is Zn-mediated stereoselective aza-Barbier reaction of imine 6 with allyl bromide to afford chiral homoallylic amine 7, and the other is ring-closing metathesis.","PeriodicalId":19688,"journal":{"name":"Organic Chemistry International","volume":"26 1","pages":"150-156"},"PeriodicalIF":0.0,"publicationDate":"2014-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88192052","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
Water Mediated Synthesis of N′-Arylmethylene-4,5,6,7-tetrahydro-2H-indazole-3-carbohydrazide Library 水介导合成N ' -芳基亚甲基-4,5,6,7-四氢- 2h -吲唑-3-碳酰肼文库
Organic Chemistry International Pub Date : 2014-10-15 DOI: 10.1155/2014/567053
M. Savant, A. M. Pansuriya, Chirag V. Bhuva, N. Kapuriya, Y. Naliapara
{"title":"Water Mediated Synthesis of N′-Arylmethylene-4,5,6,7-tetrahydro-2H-indazole-3-carbohydrazide Library","authors":"M. Savant, A. M. Pansuriya, Chirag V. Bhuva, N. Kapuriya, Y. Naliapara","doi":"10.1155/2014/567053","DOIUrl":"https://doi.org/10.1155/2014/567053","url":null,"abstract":"A novel two-step synthesis of 4,5,6,7-tetrahydro-2H-indazole-3-carbohydrazide has been developed. The library of N′-arylmethylene-4,5,6,7-tetrahydro-2H-indazole-3-carbohydrazide was generated by coupling of hydrazide to various aromatic and heterocyclic aldehydes in water media at ambient temperature with great flexibility regarding reaction time and yield.","PeriodicalId":19688,"journal":{"name":"Organic Chemistry International","volume":"21 1","pages":"1-4"},"PeriodicalIF":0.0,"publicationDate":"2014-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77145968","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
Microwave-Assisted Three-Component “Catalyst and Solvent-Free” Green Protocol: A Highly Efficient and Clean One-Pot Synthesis of Tetrahydrobenzo[b]pyrans 微波辅助三组分“无催化剂和溶剂”绿色方案:高效、清洁的一锅合成四氢苯并吡喃[b]
Organic Chemistry International Pub Date : 2014-09-17 DOI: 10.1155/2014/851924
S. Santra, Matiur Rahman, A. Roy, A. Majee, A. Hajra
{"title":"Microwave-Assisted Three-Component “Catalyst and Solvent-Free” Green Protocol: A Highly Efficient and Clean One-Pot Synthesis of Tetrahydrobenzo[b]pyrans","authors":"S. Santra, Matiur Rahman, A. Roy, A. Majee, A. Hajra","doi":"10.1155/2014/851924","DOIUrl":"https://doi.org/10.1155/2014/851924","url":null,"abstract":"A green and highly efficient method has been developed for the one-pot synthesis of tetrahydrobenzo[b]pyrans via a three-component condensation of aldehydes, 1,3-cyclic diketones, and malononitrile under MW irradiation without using any catalyst and solvent. This transformation presumably occurs by a sequential Knoevenagel condensation, Michael addition, and intramolecular cyclization. Operational simplicity, solvent and catalyst-free conditions, the compatibility with various functional groups, nonchromatographic purification technique, and high yields are the notable advantages of this procedure.","PeriodicalId":19688,"journal":{"name":"Organic Chemistry International","volume":"38 1","pages":"1-8"},"PeriodicalIF":0.0,"publicationDate":"2014-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81547661","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: 11
A Novel Regiospecific Synthesis of 1-Chloro-2-arylcyclohexenes 一种新的区域特异性合成1-氯-2-芳基环己烯
Organic Chemistry International Pub Date : 2014-07-10 DOI: 10.1155/2014/871595
Lokesh Krishnappa, H. Suresh
{"title":"A Novel Regiospecific Synthesis of 1-Chloro-2-arylcyclohexenes","authors":"Lokesh Krishnappa, H. Suresh","doi":"10.1155/2014/871595","DOIUrl":"https://doi.org/10.1155/2014/871595","url":null,"abstract":"An efficient high yielding chemoselective synthesis of eleven novel 1-chloro-2-arylcyclohexenes employing the Suzuki cross coupling of 1-bromo-2-chlorocyclohexene with eleven different aryl boronic acids and Pd(dppf) catalyst is reported.","PeriodicalId":19688,"journal":{"name":"Organic Chemistry International","volume":"39 1","pages":"133-138"},"PeriodicalIF":0.0,"publicationDate":"2014-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76542898","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
Kinetic and Mechanistic Investigation of Pyrano[2,3-d]pyrimidine Formation in the Presence of Catalyst under Novel One-Pot Three-Component Reaction 新型一锅三组分反应下吡喃[2,3-d]嘧啶生成动力学及机理研究
Organic Chemistry International Pub Date : 2014-05-11 DOI: 10.1155/2014/210327
S. Habibi‐Khorassani, M. Maghsoodlou, M. Shahraki, Sadegh Talaiefar, Jasem Aboonajmi
{"title":"Kinetic and Mechanistic Investigation of Pyrano[2,3-d]pyrimidine Formation in the Presence of Catalyst under Novel One-Pot Three-Component Reaction","authors":"S. Habibi‐Khorassani, M. Maghsoodlou, M. Shahraki, Sadegh Talaiefar, Jasem Aboonajmi","doi":"10.1155/2014/210327","DOIUrl":"https://doi.org/10.1155/2014/210327","url":null,"abstract":"Sodium acetate was applied as an efficient catalyst for the one-pot, three-component condensation reactions consisting of 4-nitrobenzaldehyde 2, malononitrile 3, and thiobarbituric acid 1. Use of nontoxic reaction components, short reaction times, environmental, easy work-up, and high yields are some remarkable advantages of this method. Kinetics and mechanism of the reaction were spectrally studied and the second order rate constant (kovr = k1) was automatically calculated by the standard equations contained within the program. The second order rate constant [Ln(kovr = k1), Ln(kovr = k1)/T] that depended on reciprocal temperature was in good agreement with the Arrhenius and Eyring equations, respectively. This data provided the suitable plots for calculating the activation energy and parameters (Ea, ΔG‡, ΔS‡, and ΔH‡) of the reaction. Furthermore, from studying the effects of solvent, concentration, and catalyst on the reaction rate, useful information was obtained regarding the mechanism. The results showed that the first step of the reaction mechanism is a rate determining step (RDS). The proposed mechanism was confirmed in accordance with the experimental data and also the steady state approximation.","PeriodicalId":19688,"journal":{"name":"Organic Chemistry International","volume":"97 1","pages":"1-10"},"PeriodicalIF":0.0,"publicationDate":"2014-05-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72915934","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
Synthesis of Ibuprofen Using Silica-Supported Preyssler Nanoparticles as an Eco-Friendly, Inexpensive, and Efficient Catalyst 二氧化硅负载的Preyssler纳米颗粒作为环保、廉价、高效的催化剂合成布洛芬
Organic Chemistry International Pub Date : 2014-05-06 DOI: 10.1155/2014/906801
A. Gharib, N. Pesyan, L. V. Fard, M. Roshani
{"title":"Synthesis of Ibuprofen Using Silica-Supported Preyssler Nanoparticles as an Eco-Friendly, Inexpensive, and Efficient Catalyst","authors":"A. Gharib, N. Pesyan, L. V. Fard, M. Roshani","doi":"10.1155/2014/906801","DOIUrl":"https://doi.org/10.1155/2014/906801","url":null,"abstract":"This paper describes an alternative and simple procedure for the synthesis of Ibuprofen using Silica-Supported Preyssler Nanoparticles (H14[NaP5W30O110]/SiO2) (SPNPs), as an eco-friendly, inexpensive, and efficient catalyst. High yields, simplicity of operation, and easy work-up procedure are some advantages of this protocol. Silica-Supported Preyssler Nanoparticles (H14[NaP5W30O110]/SiO2) (SPNPs) offer the advantages of a higher hydrolytic and thermal stability. The salient features of Preyssler’s anion are availability, nontoxicity and reusability. We believe this methodology can find usefulness in organic synthesis.","PeriodicalId":19688,"journal":{"name":"Organic Chemistry International","volume":"27 1","pages":"1-6"},"PeriodicalIF":0.0,"publicationDate":"2014-05-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85564552","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: 6
Synthesis of Novel Symmetrical and Unsymmetrical o-Phthalic Acid Diamides 新型对称和不对称邻苯二甲酸二胺的合成
Organic Chemistry International Pub Date : 2014-05-05 DOI: 10.1155/2014/576715
P. Kumar, Y. D. Reddy, C. V. Reddy, B. Devi, P. Dubey
{"title":"Synthesis of Novel Symmetrical and Unsymmetrical o-Phthalic Acid Diamides","authors":"P. Kumar, Y. D. Reddy, C. V. Reddy, B. Devi, P. Dubey","doi":"10.1155/2014/576715","DOIUrl":"https://doi.org/10.1155/2014/576715","url":null,"abstract":"Phthalic anhydride was treated with secondary amines in acetic acid yielding 2-(diethyl (or) 4-alkylpiperazine or morpholine-1-carbonyl) benzoic acids. The latter were reacted, again, with secondary amines and arylamines by using the coupling reagent HATU and Et3N as a base in DMF giving the novel symmetrical o-phthalic acid diamides , unsymmetrical o-phthalic acid diamides , and primary amidic-secondary amidic containing unsymmetrical o-phthalic acid diamides , respectively.","PeriodicalId":19688,"journal":{"name":"Organic Chemistry International","volume":"42 1","pages":"1-9"},"PeriodicalIF":0.0,"publicationDate":"2014-05-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73505850","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
Glycerol Containing Triacetylborate Mediated Syntheses of Novel 2-Heterostyryl Benzimidazole Derivatives: A Green Approach 含三乙酰硼酸酯甘油介导的新型2-杂苯乙烯基苯并咪唑衍生物的合成:绿色途径
Organic Chemistry International Pub Date : 2014-04-27 DOI: 10.1155/2014/260726
Ashok Kumar Taduri, P. K. Babu, B. Devi
{"title":"Glycerol Containing Triacetylborate Mediated Syntheses of Novel 2-Heterostyryl Benzimidazole Derivatives: A Green Approach","authors":"Ashok Kumar Taduri, P. K. Babu, B. Devi","doi":"10.1155/2014/260726","DOIUrl":"https://doi.org/10.1155/2014/260726","url":null,"abstract":"A very simple, mild, efficient, and novel green methodology has been developed for the syntheses of some 2-hetero/styryl-benzimidazoles. Title compounds were synthesized by the condensation of -phenylenediamine with cinnamic acids at 150–180°C for 5-6 h using glycerol containing triacetylborate (10–20 mol%) as the reaction medium. In an alternative approach, condensation of 2-methylbenzimidazole derivatives with aromatic aldehydes was done using glycerol containing triacetylborate (10–20 mol%) as the reaction medium.","PeriodicalId":19688,"journal":{"name":"Organic Chemistry International","volume":"57 4 1","pages":"1-9"},"PeriodicalIF":0.0,"publicationDate":"2014-04-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90113276","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
Synthesis and Antimicrobial Activities of N-(Heteroaryl-substituted)-p-toluenesulphonamides N-(杂芳基取代)-对甲苯磺酰胺的合成及抗菌活性研究
Organic Chemistry International Pub Date : 2014-04-15 DOI: 10.1155/2014/748257
Ozoh Chinwe Francisca, O. U. Chris, Ugwu D. Izuchukwu
{"title":"Synthesis and Antimicrobial Activities of N-(Heteroaryl-substituted)-p-toluenesulphonamides","authors":"Ozoh Chinwe Francisca, O. U. Chris, Ugwu D. Izuchukwu","doi":"10.1155/2014/748257","DOIUrl":"https://doi.org/10.1155/2014/748257","url":null,"abstract":"A new class of N-(heteroaryl-substituted)-p-toluenesulphonamides has been synthesized exhibiting antibacterial and antifungal properties. The condensation reaction of p-toluenesulphonyl chloride 1 with appropriate substituted amino pyridines 2a–g in acetone furnished N-(heteroaryl-substituted)-p-toluenesulphonamides 3a–g. These derivatives were characterized by IR, 1H-, and 13C-NMR spectroscopy and were screened in vitro against gram-positive bacteria, gram-negative bacteria, and fungi organisms using agar-diffusion method. Results indicated improved biological activities over reference drugs such as Tetracycline (TCN) and Fluconazole (FLU).","PeriodicalId":19688,"journal":{"name":"Organic Chemistry International","volume":" 11","pages":"1-5"},"PeriodicalIF":0.0,"publicationDate":"2014-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91415187","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
An Efficient Method for Synthesis of N-tert-Butyl Amides Using Oxalic Acid Dihydrate in Solvent-Free Condition 无溶剂条件下二水合草酸合成n -叔丁基酰胺的高效方法
Organic Chemistry International Pub Date : 2014-04-08 DOI: 10.1155/2014/617153
M. Mokhtary, Seyedeh Khadijeh Nasernezhad
{"title":"An Efficient Method for Synthesis of N-tert-Butyl Amides Using Oxalic Acid Dihydrate in Solvent-Free Condition","authors":"M. Mokhtary, Seyedeh Khadijeh Nasernezhad","doi":"10.1155/2014/617153","DOIUrl":"https://doi.org/10.1155/2014/617153","url":null,"abstract":"An efficient method for the synthesis of N-tert-butyl amides by reaction of nitriles with tert-butyl acetate or tert-butanol is described using oxalic acid dihydrate in solvent-free condition. The result showed that tert-butyl acetate served as a relatively better source of tert-butyl carbocation than tert-butanol.","PeriodicalId":19688,"journal":{"name":"Organic Chemistry International","volume":"12 1","pages":"85-88"},"PeriodicalIF":0.0,"publicationDate":"2014-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73269225","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
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
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
请完成安全验证×
相关产品
×
本文献相关产品
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号：481959085
Book学术官方微信