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Abstract
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Abstract
Synth. Commun. 2006, 36, 3461
A CLOSER LOOK AT THE HYDROIODINATION OF PROPIOLIC ACID
James P. Donahue
Department of Chemistry, Tulane University, New Orleans, LA, USA
The product isolated from the hydroiodination of propiolic acid is found to dependent upon the specific reaction conditions employed.
Abstract
Synth. Commun. 2006, 36, 3473
RECYCLABLE AND LIGANDLESS SUZUKI COUPLING CATALYZED BY CARBON NANOTUBE‐SUPPORTED PALLADIUM NANOPARTICLES SYNTHESIZED IN SUPERCRITICAL FLUID
Horng‐Bin Pan, Clive H. Yen, Byunghoon Yoon, Masaki Sato, and Chien M. Wai
Department of Chemistry, University of Idaho, Moscow, Idaho, USA
Carbon nanotube‐supported palladium nanoparticles prepared by a supercritical fluid deposition method show high activities for catalyzing Suzuki coupling reactions and the catalysts can be recycled and reused at least six times without losing activity.
Abstract
Synth. Commun. 2006, 36, 3479
ONE‐POT SYNTHESIS OF OXIME DERIVATIVES OF 1,3‐DIPHENLYPYRAZOLE‐4‐CARBOXALDEHYDES FROM ACETOPHENONE PHENYLHYDRAZONES USING VILSMEIER–HAACK REAGENT
Om Prakash,1 Kamaljeet Pannu,1 Rajesh Naithani,1 and Harpreet Kaur2
1Department of Chemistry, Kurukshetra University, Kurukshetra, India
2Department of Pharamaceutical Sciences, Wayne State University, Detroit, MI, USA
A one‐pot synthesis of oxime derivatives 3a–3f of 1‐phenyl‐3‐arylpyrazole‐4‐carboxaldehydes has been accomplished by the Vilsmeier–Haack reaction of acetophenone phenylhydrazones 1a–1f under a new workup procedure.
Abstract
Synth. Commun. 2006, 36, 3487
CONVENIENT SYNTHESIS OF N,N′‐BIS‐PROTECTED‐3,3′‐DIIODO‐2,2′‐BIINDOLES
Sudipta Roy and Gordon W. Gribble
Department of Chemistry, Dartmouth College, Hanover, New Hampshire, USA
Abstract
Synth. Commun. 2006, 36, 3493
FACILE ONE‐POT SYNTHESIS OF 2‐ARYL‐SUBSTITUTED NITRILES AND 2‐ARYL‐3‐KETO NITRILES VIA BENZYNE REACTION
Sukanta Kamila, Benjamin Koh, and Edward R. Biehl
Southern Methodist University, Dallas, TX, USA
Abstract
Synth. Commun. 2006, 36, 3509
SELECTIVE APICAL BROMINATION OF DIAMANTANE AND CONVERSION TO THE DIHYDROXY AND DICARBOXYLIC ACID DERIVATIVES
Matthew C. Davis1 and Shenggao Liu2
1Chemistry and Materials Division, Michelson Laboratory, Naval Air Warfare Center, China Lake, CA, USA
2MolecularDiamond Technologies, Chevron Technology Ventures, LLC, Richmond, CA, USA
Abstract
Synth. Commun. 2006, 36, 3515
SYNTHESIS OF A THIOPHENE‐BASED NONLINEAR OPTICAL CHROMOPHORE
Matthew C. Davis, Richard A. Hollins, and Brad Douglas
Chemistry and Materials Division, Michelson Laboratory, Naval Air Warfare Center, China Lake, CA, USA
The chromophore was synthesized in eight steps in 38% overall yield.
Abstract
Synth. Commun. 2006, 36, 3525
SYNTHESIS OF 2‐OXO‐7‐SULFAMOYL‐2,3,4,5‐TETRAHYDRO‐1H‐BENZO [B]AZEPINES
Mikhail V. Dorogov,1 Sergey A. Ivanovsky,1 Maria Y. Khakhina,1 Dmitry V. Kravchenko,2 Sergey E. Tkachenko,3 and Alexandre V. Ivachtchenko3
1Ushinsky Yaroslavl State Pedagogical University, Yaroslavl, Russia
2Chemical Diversity Research Institute, Khimki, Moscow, Russia
3ChemDiv, Inc., San Diego, California, USA
Novel amide derivatives of 2‐оxo‐7‐sulfonyl‐2,3,4,5‐tetrahydro‐1H‐benzo[b]azepine were efficiently prepared starting from 2‐oxo‐2,3,4,5‐tetrahydro‐1H‐benzo[b]azepine.
Abstract
Synth. Commun. 2006, 36, 3537
PRACTICAL SYNTHESIS OF N‐ALKYL‐N‐ALKYLOXYCARBONYLAMINOMETHYL PRODRUG DERIVATIVES OF ACETAMINOPHEN, THEOPHYLLINE, AND 6‐MERCAPTOPURINE
Susruta Majumdar and Kenneth B. Sloan
Department of Medicinal Chemistry, University of Florida, Gainesville, FL, USA
Abstract
Synth. Commun. 2006, 36, 3549
REGIOSELECTIVE N‐ARYLATION OF SOME PYRIMIDINE AND PURINE NUCLEOBASES
Ali Khalafi‐Nezhad,1 Abdolkarim Zare,1 Abolfath Parhami,1 Mohammad Navid Soltani Rad,2 and Gholam Reza Nejabat1
1Department of Chemistry, College of Sciences, Shiraz University, Shiraz, Iran
2Department of Chemistry, College of Basic Sciences, Shiraz University of Technology, Shiraz, Iran
Abstract
Synth. Commun. 2006, 36, 3563
NEW PROTOCOL TO SYNTHESIZE SPIRO‐1,4‐DIHYDROPYRIDINES BY USING A MULTICOMPONENT REACTION OF CYCLOHEXANONE, ETHYL CYANOACETATE, ISATIN, AND PRIMARY AMINES UNDER MICROWAVE IRRADIATION
Farhad Hatamjafari
Department of Chemistry, Faculty of Science, Islamic Azad University‐Tonekabon Branch, Tonekabon, Iran
Abstract
Synth. Commun. 2006, 36, 3571
APPLICATION OF ALKALI METAL HYDROXIDES FOR THE PREPARATION OF GEM‐CHLOROPHENYLCYCLOPROPANES
Andrzej Jończyk, Hanna Karwowska, and Jolanta Furman
Faculty of Chemistry, Warsaw University of Technology, Warszawa, Poland
Abstract
Synth. Commun. 2006, 36, 3581
SYNTHESIS OF NEW QUINOLINE DERIVATIVES
Judit Tóth, Gábor Blaskó, András Dancsó, László Tőke, and Miklós Nyerges
Department of Organic Chemical Technology, Budapest University of Technology and Economics, Budapest, Hungary
Abstract
Synth. Commun. 2006, 36, 3591
ATYPICAL OXIDATION REACTION BY THIONYL CHLORIDE: EASY TWO‐STEP SYNTHESIS OF N‐ALKYL‐1,4‐DITHIINES
Alain Valla, Dominique Cartier, Frédéric Zentz, and Roger Labia
Chimie et Biologie des Substances Naturelles FRE 2125 CNRS 6, rue de l'Université, 29000 Quimper, France
Abstract
Synth. Commun. 2006, 36, 3599
KF/Al2O3‐MEDIATED N‐ALKYLATION OF AMINES AND NITROGEN HETEROCYCLES IN AND S‐ALKYLATION OF THIOLS
Firouz Matloubi Moghaddam, Seyedeh Maryam DokhtTaimoory, Hossein Ismaili, and Ghasem Rezanejade Bardajee
Department of Chemistry, Sharif University of Technology, Tehran, Iran
Different types of amines and thiols react smoothly with various alky halides in the presence of KF/Al2O3 to afford corresponding N‐alkylated amines and thioethers.
Abstract
Synth. Commun. 2006, 36, 3609
EFFICIENT AND MILD PROCEDURE FOR REDUCTIVE METHYLATION OF AMINES USING N‐METHYLPIPERIDINE ZINC BOROHYDRIDE
Heshmatollah Alinezhad, Mahmood Tajbakhsh, and Reza Zamani
Department of Chemistry, Mazandaran University, Babolsar, Iran
N‐Methylpiperidine zinc borohydride (ZBNMPP) is an efficient reagent for the reductive methylation of primary and secondary amines, giving the corresponding tertiary methylated amines in high yield.
Abstract
Synth. Commun. 2006, 36, 3617
EFFICIENT APPROACH FOR THE SYNTHESIS OF NOVEL FUNCTIONALIZED ISOXAZOLINES FROM LIMONENE
Amal Feddouli,1 My Youssef Ait Itto,1 Mustapha Ait Ali,1 Aïssa Hasnaoui1, and Abdelkhalek Riahi2
1Department of Chemistry, Faculty of Science‐Semlalia, BP 2390, Marrakech, Morocco
2Unity of research ≪Selective Reactions and Applications≫ NCSR, University of Rheims Champagne‐Ardenne, Rheims, France
Convenient and efficient synthesis of new isoxazolyl‐ketoacids from limonene is reported.
Abstract
Synth. Commun. 2006, 36, 3625
ZEOLITE‐CATALYZED ENVIRONMENTALLY FRIENDLY SYNTHESIS OF BENZIMIDAZOLE DERIVATIVES
Adrienn Hegedüs, Zoltán Hell, and Attila Potor
Department of Organic Chemical Technology, Budapest University of Technology and Economics, H‐1521, Budapest, Hungary
Abstract
Synth. Commun. 2006, 36, 3631
REACTIONS OF 6‐AMINOURACILS: THE FIRST SIMPLE, FAST, AND HIGHLY EFFICIENT SYNTHESIS OF BIS(6‐AMINOPYRIMIDONYL)METHANES (BAPMS) USING THERMAL OR MICROWAVE‐ASSISTED SOLVENT‐FREE METHODS
Javad Azizian,1 Mohammad R. Mohammadizadeh,1 Fatemeh Teimouri,2 Ali A. Mohammadi,1 and Ali R. Karimi1
1Chemistry Department, Shahid Beheshti University, Tehran, Iran
2Department of Chemistry, Science and Research Campus, Islamic Azad University, Tehran, Iran
Abstract
Synth. Commun. 2006, 36, 3639
RAPID SYNTHESIS OF NEW 5‐NITROIMIDAZOLES AS POTENTIAL ANTIBACTERIAL DRUGS VIA VNS PROCEDURE
Maxime D. Crozet, Vincent Rémusat, Christophe Curti, and Patrice Vanelle
Laboratoire de Chimie Organique Pharmaceutique, UMR–CNRS 6517, Faculté de Pharmacie, Marseille, France
Original 4‐arylsulfonylmethyl‐5‐nitroimidazoles were prepared by reacting four chloromethylaryl sulfones with 5‐nitroimidazole derivatives via a VNS reaction.
