Abstract
Graphical Abstract Section
Abstract
Synth. Commun. 2007, 37, 2815
MICROWAVE‐ASSISTED ONE-POT SYNTHESIS OF 2-(SUBSTITUTED PHENYL)-1H-BENZIMIDAZOLE DERIVATIVES
Gabriel Navarrete-Vazquez,1 Hermenegilda Moreno-Diaz,1 Mariana Torres-Piedra,1 Ismael León-Rivera,2 Hugo Tlahuext,2 Omar Muñoz-Muñiz,3 Hector Torres-Gómez,4 and Samuel Estrada-Soto1
1Facultad de Farmacia, Universidad Autónoma del Estado de Morelos, Cuernavaca, México
2Centro de Investigaciones Químicas, Universidad Autónoma del Estado de Morelos, Cuernavaca, México
3Unidad de Servicios de Apoyo en Resolución Analítica, Universidad Veracruzana, México
4Facultad de Ciencias, Universidad Autónoma del Estado de Morelos, Cuernavaca, México
A simple, fast, and efficient method for the preparation of several benzimidazole derivatives is reported. Compounds were synthesized via microwave irradiation using a short synthetic route and solvent-free conditions.
Abstract
Synth. Commun. 2007, 37, 2827
NOVEL CYANOKETENE N,S-ACETALS AND PYRAZOLE DERIVATIVES USING POTASSIUM 2-CYANOETHYLENE-1-THIOLATES
Galal H. Elgemeie,1 Ahmed H. Elghandour,2 and Ghada W. Abd Elaziz2
1Chemistry Department, Faculty of Science, Helwan University, Helwan, Cairo, Egypt
2Chemistry Department, Faculty of Science, Cairo University, Beni-Suef Branch, Beni-Suef, Egypt
Novel keten N,S-acetals 3 were readily prepared by the reaction of activated nitriles 1a,b with phenylisothiocyanate in the presence of potassium hydroxide, followed by alkylation of the produced salts 2 with methyl iodide. The reaction of compounds 3 with hydrazines afforded difference substituted pyrazoles 6.
Abstract
Synth. Commun. 2007, 37, 2835
ASYMMETRIC INDUCTION THROUGH METALATION OF CHIRAL DITHIOACETALS AND OXTHIOACETALS
Javid. H. Zaidi and Naseem Iqbal Gunjial
Department of Chemistry, Quaid‐i‐Azam University, Islamabad, Islamabad, Pakistan
Abstract
Synth. Commun. 2007, 37, 2847
EFFICIENT AND INDUSTRIALLY VIABLE SYNTHESIS OF DONEPEZIL
R. Janaki Rama Rao,1 A. K. S. Bhujanga Rao,1 and Y. L. N. Murthy2
1Natco Research Centre, Natco Pharma Ltd., Hyderabad, Andhra Pradesh, India
2Department of Organic Chemistry, Andhra University, Visakhapatnam, Andhra Pradesh, India
Abstract
Synth. Commun. 2007, 37, 2855
SYNTHESIS OF (±)-AR-MACROCARPENE
A. Srikrishna and B. Beeraiah
Department of Organic Chemistry, Indian Institute of Science, Bangalore, India
Abstract
Synth. Commun. 2007, 37, 2861
EFFICIENT SYNTHESIS OF N-OXIDE DERIVATIVES: SUBSTITUTED 2-(2-(PYRIDYL-N-OXIDE)METHYLSULPHINYL)BENZIMIDAZOLES
Purna C. Ray, Vasantha Mittapelli, Amit Rohatgi, and Om Dutt Tyagi
Matrix Laboratories Limited, Medak Dist, India
Abstract
Synth. Commun. 2007, 37, 2869
IONIC LIQUID–PROMOTED STEREOSELECTIVE SYNTHESIS OF (Z)-VINYL BROMIDES BY [BMIM]OH UNDER ORGANIC SOLVENT–FREE CONDITIONS: A GREEN APPROACH
Brindaban C. Ranu, Subhash Banerjee, and Jhinuk Gupta
Department of Organic Chemistry, Indian Association for the Cultivation of Science, Jadarpur, Kolkata, India
Abstract
Synth. Commun. 2007, 37, 2877
CYCLOPENTYL: A NOVEL PROTECTIVE GROUP FOR PHENOLS
Jitendra M. Gajera, Laxmikant A. Gharat, and Aniket V. Farande
Drug Discovery Chemistry, Glenmark Research Centre, Navi Mumbai, India
Abstract
Synth. Commun. 2007, 37, 2881
STANNIC CHLORIDE–IODINE: AN EFFICIENT REAGENT FOR REGIOSELECTIVE SYNTHESIS OF FURAN–FUSED HETEROCYCLES
K. C. Majumdar, A. Biswas, and P. P. Mukhopadhyay
Department of Chemistry, University of Kalyani, Kalyani, West Bengal, India
Abstract
Synth. Commun. 2007, 37, 2891
EFFICIENT SYNTHESIS OF TERT-BUTYL ETHERS UNDER SOLVENT-FREE CONDITIONS
Neithnadka Premsai Rai and Pirama Nayagam Arunachalam
Syngene International Pvt. Ltd., Bangalore, India
A simple and efficient synthesis of tert-butyl ethers from various alcohols and substituted phenols using tert-butyl bromide in the presence of basic lead carbonate as a catalyst. The catalyst is easily recovered via filtration and can be reused up to three times without appreciable loss of activity.
Abstract
Synth. Commun. 2007, 37, 2897
IMPROVED METHODS FOR THE SYNTHESIS OF IRBESARTAN, AN ANTIHYPERTENSIVE ACTIVE PHARMACEUTICAL INGREDIENT
Korrapati V. V. Prasada Rao,1 Ramesh Dandala,1 Vijay. K. Handa,3 Inti. V. Subramanyeswara Rao,1 Ananta Rani,1 and Andra Naidu2
1Research and Development Department, Aurobindo Pharma Ltd, Hyderabad, Andhra Pradesh, India
2Jawaharlal Nehru Technological University, Hyderabad, India
Abstract
Synth. Commun. 2007, 37, 2907
REGIOSELECTIVE SYNTHESIS OF BENZOFURAN-ANNULATED SIX-MEMBERED SULFUR HETEROCYCLES BY ARYL RADICAL CYCLIZATION
K. C. Majumdar, B. Chattopadhyay, and S. Nath
Department of Chemistry, University of Kalyani, Kalyani, West Bengal, India
Abstract
Synth. Commun. 2007, 37, 2917
SYNTHESIS OF METAL-FREE PHTHALOCYANINES IN FUNCTIONALIZED AMMONIUM IONIC LIQUIDS
S. M. S. Chauhan, Shweta Agarwal, and Pratibha Kumari
Department of Chemistry, University of Delhi, Delhi, India
Cycloteramerization of varoius phthalonitriles in the presence of DBU in different hydroxyalkylammonium ionic liquids at 120–150°C gave metal-free phthalocyanines in moderate yields
Abstract
Synth. Commun. 2007, 37, 2927
PRACTICAL SYNTHESIS OF SUGAR MONOPHOSPHONUCLEOTIDES
Wjatschesslaw A. Wlassoff, Richard M. J. Finlay, and Chris J. Hamilton
School of Chemistry and Chemical Engineering, Queens University Belfast, Belfast, U.K.
A practical method is described for preparing purine- and pyrimidine-derived sugar monophosphonucleotides from accessible glycosyl-1-H-phosphonate precursors.
Abstract
Synth. Commun. 2007, 37, 2935
1,3-DIPOLAR CYCLOADDITIONS OF ALDEHYDES OR IMINES WITH CARBONYL YLIDES GENERATED FROM EPOXIDES: CLASSICAL HEATING AND MICROWAVE IRRADIATION.
Ghenia Bentabed,1,3 Mustapha Rahmouni,2 Florence Mongin,3 Aicha Derdour,1 Jack Hamelin,4 and Jean Pierre Bazureau4
1Laboratoire de Synthèse Organique Appliquée, Faculté des Sciences, Oran, Algérie
2Laboratoire de Synthèse Organique et Catalyse, Université Ibn Khaldoun, Tiaret, Algérie
3Synthèse and Electro Synthèse Organiqes, Université de Rennes 1, Rennes Cedex, France
4Sciences Chimiques de Rennes, Université de Rennes 1, Rennes Cedex, France
Abstract
Synth. Commun. 2007, 37, 2949
SYNTHESIS AND STRUCTURAL ELUCIDATION OF NOVEL BISARYLMETHYLIDENES OF CYCLIC ENONES
M. Saeed Abaee,1 Mohammad M. Mojtahedi,1 M. Mehdi Zahedi,1 Roholah Sharifi,1 A. Wahid Mesbah,1 and Werner Massa2
1Organic Chemistry Laboratory, Chemistry and Chemical Engineering Research Center of Iran, Tehran, Iran
2Fachbereich Chemie der Philipps-Universitaet Marburg, Marburg, Germany
The first procedure for the synthesis of novel bisarylmethylidenes of cyclohex-2-enone structures is described at room temperature using a mild medium consisting of anhydrous zinc bromide and triethylamine. Several compounds of this class are synthesized conveniently and rapidly. Spectroscopic and X-ray diffraction experiments confirm the proposed structures.
Abstract
Synth. Commun. 2007, 37, 2959
SYNTHESIS OF 5-CYANO-1,3-DIOXOALKANES BY REACTION OF 1,3-DICARBONYL DIANIONS WITH BROMOACETONITRILE
Edith Holtz1 and Peter Langer2,3
1Institut für Organische Chemie, Georg-August-Universität Göttingen, Göttingen, Germany
2Institut für Chemie, Universität Rostock, Rostock, Germany
3Leibniz-Institut für Katalyse e. V. an der Universität Rostock, Rostock, Germany
Abstract
Synth. Commun. 2007, 37, 2967
DABCO–BROMINE COMPLEX: A NOVEL OXIDIZING AGENT FOR OXIDATIVE DEPROTECTION OF THP AND SILYL ETHERS AND SEMICARBAZONES TO CORRESPONDING CARBONYL COMPOUNDS
Mahmood Tajbakhsh,1 Majid M. Heravi,2 and Setareh Habibzadeh1 1Department of Chemistry, School of Sciences, Mazandaean University, Babolsar, Iran
2Department of Chemistry, School of Sciences, Azzáhero University, Vanak, Tehran, Iran
Abstract
Synth. Commun. 2007, 37, 2975
ASYMMETRIC SYNTHESIS AND CHARACTERIZATION OF CHIRAL 2,2′-DIAMINO-3,3′-DIETHOXYCARBONYL-8,8′-DIPHENYL-1,1′-BIAZULENE
Arh-Hwang Chen, Hsiu-Hang Yen Yu-Chen Kuo, and Wen-Zhang Chen
Department of Chemical and Materials Engineering, Southern Taiwan University of Technology, Yung-Kang City, Taiwan
Abstract
Synth. Commun. 2007, 37, 2989
CONCISE SYNTHESIS OF PENTENYL PHENYL ACRYLIC ACID
Dequn Sun,1 Pengxiang Lai,1 Weidong Xie,1 Jingen Deng,2 and Yaozhong Jiang2
1Marine College, Shandong University at Weihai, China
2Chengdu Institute of Organic Chemistry, CAS, China
A new synthetic strategy was developed to prepare pentenyl phenyl acrylic acid 15, the important component of Pepticinnamin E, with high stereoselectivity and high overall yield of 78.6% in five step procedure.
Abstract
Synth. Commun. 2007, 37, 2995
SHORT AND EFFICIENT SYNTHESIS OF THIOLS GROUP FUNCTIONALIZED CROWN ETHER
Yong Sun,1 Xiaoxia Lu,2 Rui Wang,1 Lin Shi,2 and Bin Yang1
1Department of Chemistry, Sichuan University, Chengdu, P. R. China
2Chengdu Institute of Biology, Chinese Academic of Sciences Chengdu, P. R. China
Mercaptobenzocrown SH-B15C5 and SH-B18C6 (B15C5=Benzo-15-crown-5; B18C6= Benzo-18-crown-6) have been synthesized from direct chlorosulfonation of simple crown ether with chlorosulfonic acid and then reduction of the sulfonyl chloride moiety with LiAlH4. This work describes a short and efficient synthetic method for thiols group functionalized crown ethers.
Abstract
Synth. Commun. 2007, 37, 3003
HIGHLY EFFICIENT AILS/L‐PROLINE SYNERGISTIC CATALYZED THREE‐COMPONENT ASYMMETRIC MANNICH REACTION
Baoyou Liu,1 Danqian Xu,2 Jianfang Dong,1 Huilong Yang,1 Dishun Zhao,3 Shuping Luo,2and Zhenyuan Xu2
1College of Environmental Science and Engineering, Hebei University of Science and Technology, Shijiazhuang, China
2Catalytic Hydrogenation Research Center, Zhejiang University of Technology, Hangzhou, China
3College of Chemical and Pharmaceutical Engineering, Hebei University of Science and Technology, Shijiazhuang, China
A series of β‐amino ketones were prepared through asymmetric Mannich reaction of isovaleraldehyde, methyl ketones and aromatic amines synergistic catalyzed by AILs/L‐Proline with high yields and enantioselectivities under mild conditions.
Abstract
Synth. Commun. 2007, 37, 3011
SO4 2−/SNO2: EFFICIENT, CHEMOSELECTIVE AND REUSABLE CATALYST FOR ACYLATION OF ALCOHOLS, PHENOLS, AND AMINES AT ROOM TEMPERATURE
Jitendra R. Satam, Manoj B. Gawande, Sameer S. Deshpande, and Radha V. Jayaram
Department of Chemistry, University Institute of Chemical Technology, Mumbai, India