Abstract
Synth. Commun. 2003, 33, 4185
Mild and Efficient Deoxygenation of Amine- N -oxides with Titanium Tetrachloride-Indium System
Byung Woo Yoo,1,* Kwang Hyun Choi,1 Kyung Il Choi,2 and Joong Hyup Kim2
1Department of Advanced Material Chemistry, Korea University, Jochiwon, Chungnam, South Korea; 2Biochemicals Research Center, Korea Institute of Science and Technology, Cheongryang, Seoul, South Korea
Abstract
Synth. Commun. 2003, 33, 4191
Synthesis of Annularly Functionalized Dicationic Benzimidazolophanes and Benzotriazolophanes
Perumal Rajakumar,* Venghatraghavan Murali, and Kilivelu Ganesan
Department of Organic Chemistry, University of Madras, Guindy Campus, Chennai, India
Abstract
Synth. Commun. 2003, 33, 4199
Rapid Access to Tricyclic Systems: Highly Endoselective Diels-Alder Reaction of Cycloalkenones with Cyclic Dienes Under Microwave Irradiation
M. Karthikeyan, R. Kamakshi, V. Sridar, B. S. R. Reddy*
Industrial Chemistry Laboratory, Central Leather Research Institute, Adyar, Chennai, India
Abstract
Synth. Commun. 2003, 33, 4205
A Simple and Efficient Method for the Reduction of Azo Compounds
Chang-Rui Zhang1 and Yu-Lu Wang2,*
1College of Chemistry and Environmental Science of Henan Normal University, Henan Xinxiang, P.R. China; 2The Key Laboratory of Environmental Science and Technology of High Education of Henan Province, P.R. China
Abstract
Synth. Commun. 2003, 33, 4209
A Versatile Method for the Preparation of Enantiomeric Benzene-1,2- bis (alanine) Derivatives
Bjørg S. Møller and Kjell Undheim*
Department of Chemistry, University of Oslo, Oslo, Norway
Diels-Alder adduct formation with a stereoselectively prepared diene bis(α-amino acid) has provided substituted (R,R)-benzene, -dihydrobenzene-, and tetrahydrobenzene-1,2-bis(alanine) derivatives.
Abstract
Synth. Commun. 2003, 33, 4221
Lead-Catalyzed Synthesis of Azo Compounds by Ammonium Acetate Reduction of Aromatic Nitro Compounds
G. R. Srinivasa, K. Abiraj, and D. Channe Gowda*
Department of Studies in Chemistry, University of Mysore, Manasagangotri, Mysore, Karnataka, India
Azo compounds containing additional reducible substituents such as halogen, nitrile, acid, phenol, ester, methoxy etc. functions are synthesized by reducing the corresponding nitro compounds using lead and ammonium acetate in methanol.
Abstract
Synth. Commun. 2003, 33, 4229
Facile Synthesis of Nicotinic Acid Derivatives with Unsymmetrical Substitution Patterns
Wei-Guang Zhao, Zheng-Xiao Liu, Zheng-Ming Li,* and Bao-Lei Wang
State Key Laboratory of Elemento-Organic Chemistry, Institute of Elemento-Organic Chemistry, Nankai University, Tianjin, P.R. China
The ketene N,S-acetals 2 reacted with β-ketoesters to give nicotinic acid with unsymmetrical substitution patterns derivatives 3, and the ketene dithioacetals 1 reacted β-amino-crotonates to obtain derivatives 6.
Abstract
Synth. Commun. 2003, 33, 4235
A Practical Synthesis of Lithium 3-Fluoropyridine-2-Carboxylate
Khateeta M. Emerson,2,* Robert D. Wilson,2 Michael S. Ashwood,2 Derek J. Kennedy,2 David Hands,2 Karel M. J. Brands,2 Ian F. Cottrell,2 and Ulf-H Dolling1
1Process Research, Merck Research Laboratories, Rahway, New Jersey, USA; 2Process Research, Merck Sharp and Dohme Research Laboratories, Hoddesdon, Hertfordshire, UK
Abstract
Synth. Commun. 2003, 33, 4241
Synthesis of 7-Amino-1-Nitro-2-Heptanone Derivatives
Konstantin G. Nazarenko, Konstantin V. Shvidenko,* Alexander M. Pinchuk, and Andrei A. Tolmachev
Institute of Organic Chemistry, National Academy of Sciences of Ukraine, Kyiv, Ukraine
New N-substituted 7-amino-1-nitro-2-heptanone derivatives have been obtained starting from readily accessible 2-(nitromethylidene)hexahydro-1H-azepine. These compounds have been further used as starting materials for the synthesis of some heterocycles with 5-aminopentyl fragment.
Abstract
Synth. Commun. 2003, 33, 4253
Chemoselective Protection of Carbonyl Compounds as Dithioacetals Using Silica Gel Supported Aluminium Chloride
B. Tamami* and K. Parvanak Borujeny
Department of Chemistry, College of Sciences, Shiraz University, Shiraz, Iran
Silica gel supported aluminium chloride is shown to be a mild chemoselective catalyst for dithioacetalization of carbonyl compounds.
Abstract
Synth. Commun. 2003, 33, 4259
A facile synthesis of New 3-Substituted-2,3-dihydropyrido-[3,2-d]-pyrimidine-2,4-diones
R. Mamouni,1 M. Akssira,1,* M. Aadil,1 A. Elhakmaoui,1 J. Lasri,2 and E. Zaballos-Garcia2
1Laboratoire de Chimie Bioorganique et Analytique, Université Hassan II-Mohammedia, Mohammedia, Morocco; 2Departamento de Química Orgánica, Facultad de Farmacia, Universidad de Valencia, Burjassot, Valencia, Spain
Abstract
Synth. Commun. 2003, 33, 4269
Synthesis of a Far Red Absorbing Thiobarbituric Acid Oxonol Derivative as a Fluorescent Probe for Biological Applications
Leslie W. Deady,1,* Andrew B. Hughes,1 Nectarios Klonis,2 Nurul H. Quazi,1 and Leann M. Tilley2
1Departments of Chemistry and 2Biochemistry, La Trobe University, Victoria, Australia
Abstract
Synth. Commun. 2003, 33, 4279
Microwave-Assisted Conversion of Nitriles to Thioamides in Solvent-Free Condition
Firouz Matloubi Moghaddam,* Leila Hojabri, and Mohammad Dohendou
Sharif University of Technology, Department of Chemistry, Tehran, Iran
Abstract
Synth. Commun. 2003, 33, 4285
Heteromacrocycles from Ring-Closing Metathesis of Unsaturated Furanic Ethers
Louis Cottier,* Gérard Descotes, and Yaya Soro
Université Claude-Bernard Lyon I, Laboratoire de Chimie Organique II, UMR CNRS-Université N° 5622, ESCPE - Lyon, Villeurbanne, France
Abstract
Synth. Commun. 2003, 33, 4297
Facile Syntheses of Azetidin-3-ols by Rearrangement of 2,3-Epoxypropylamines
Chang Ho Oh,1,* Chul Yun Rhim,1 Choong Ho You,1 and Jin Rai Cho2
1Department of Chemistry, Hanyang University, Sungdong-Gu, Seoul, South Korea
2Agency for Defence Development, Yuseong, Taejon, Korea
The N-alkyl-2,3-epoxypropylamines (2) were chemoselectively rearranged to the four-membered rings, N-alkylazetidin-3-ols (3).
Abstract
Synth. Commun. 2003, 33, 4303
A Novel Approach to the Synthesis of [1,2-a]Fused Polymethylenebenzimidazoles
Konstantin G. Nazarenko,* Tatyana I. Shyrokaya, Konstantin V. Shvidenko, and Andrei A. Tolmachev
Institute of Organic Chemistry, National Academy of Sciences of Ukraine, Kyiv, Ukraine
The synthesis of 2,3-dihydro-1H-pyrrolo[1,2-a]benzimidazoles and 7,8,9,10-tetrahydro-6H-azepino[1,2-a]benzimidazoles from cyclic amidines is described.
Abstract
Synth. Commun. 2003, 33, 4313
One Pot Synthesis of Methyl Aminoacetylcyanoacetates
Stylianos Hamilakis and Athanase Tsolomitis*
The Laboratory of Organic Chemistry, The School of Chemical Engineering, The National Technical University of Athens, Athens, Greece
Abstract
Synth. Commun. 2003, 33, 4321
Synthesis of Fluorinated Epoxides Opening the Way to New Hybrid Fluorocarbon-Hydrocarbon Surfactants
A. Pasc-Banu,1 O. Petrov,1 E. Perez,1 I. Rico-Lattes,1,* A. Lattes,1 G. Pozzi,2 and S. Quici2
1Laboratoire des Interactions Moléculaires et Réactivité Chimique et Photochimique, CNRS UMR 5623, Université P. Sabatier, Toulouse cedex, France; 2Centro CNR Sintesi e Stereochimica di Speciali Sistemi Organic and Dipartimento di Chimica Organica e Industriale, Milano, Italy
Abstract
Synth. Commun. 2003, 33, 4331
Highly Stereoselective Synthesis of Optically Pure C-Aryl Imines from α-L-Amino Acid Methyl Esters
Antonella Leggio,1 Adolfo Le Pera,1 Angelo Liguori,1,* Anna Napoli,2 Claudio Romeo,2 Carlo Siciliano,1 and Giovanni Sindona2
1Dipartimento di Scienze Farmaceutiche, 2Dipartimento di Chimica, Università degli Studi della Calabria, Italy
Abstract
Synth. Commun. 2003, 33, 4339
Nucleophilic Ring Enlargement of 2-Substituted-3-isothiazolones to 1,3-Thiazin-4-ones
Stylianos Hamilakis and Athanase Tsolomitis*
The Laboratory of Organic Chemistry, The School of Chemical Engineering, The National Technical University of Athens, Athens, Greece
The preparation of 1,3,-thiazin-4-ones, by a simple procedure from 2-substituted-3-isothiazolones, is described here.
Abstract
Synth. Commun. 2003, 33, 4355
Synthesis of Benzo[ b ]imidazo[1,5- d ][1,5]thiazepines. Derivatives of a Novel Ring System
K. Petrova,* O. Petrov, A. Antonova, and V. Kalcheva
University of Sofia, Faculty of Chemistry, Sofia, Bulgaria