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Abstract
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Abstract
Synth. Commun. 2006, 35, 137
TRIPHENYLPHOSPHINE–IODINE: AN EFFICIENT REAGENT SYSTEM FOR THE SYNTHESIS OF NITRILES FROM ALDOXIMES
A. Venkat Narsaiah, D. Sreenu, and K. Nagaiah
Division of Organic Chemistry, Fine Chemicals Laboratory, Indian Institute of Chemical Technology, Hyderabad 500 007, India
Abstract
Synth. Commun. 2006, 35, 141
REGIOSELECTIVE SYNTHESIS OF NOVEL SPIROOXINDOLO AND SPIROINDANO NITRO PYRROLIDINES THROUGH 3 + 2 CYCLOADDITION REACTION
Mahalingam Poornachandran, Rajendran Muruganantham, and Ragavachary Raghunathan
Department of Organic Chemistry, University of Madras, Guindy Campus, Chennai 600 025, India
Abstract
Synth. Commun. 2006, 35, 151
SYNTHESIS OF NOVEL OXIME FUNCTIONALIZED ALDOL PRODUCTS VIA MICHAEL ADDITION OF OXIMES ONTO BAYLIS–HILLMAN ADDUCTS
Debnath Bhuniya, Srinivas Gujjary, and Sujata Sengupta
Metabolic Disorder (Chemistry) Group, Dr. Reddy's Laboratories Ltd.—Discovery Research, Miyapur, Bollaram Road, Hyderabad 500 049, India
Abstract
Synth. Commun. 2006, 35, 165
DMSO/NaNO2/49% HBr: A NOVEL AND POWERFUL OXIDANT FOR THE DIRECT CONVERSION OF PRIMARY BENZYLAMINES TO BENZOIC ACIDS
Ramesh Naik and M. A. Pasha
Department of Studies in Chemistry, Central College Campus, Bangalore University, Bangalore 560 001, India
A mixture of DMSO, NaNO2, and 49% HBr is found to oxidize primary benzylamines to benzoic acids at 100°C.
Abstract
Synth. Commun. 2006, 35, 169
NEW SYNTHESIS OF DONEPEZIL THROUGH PALLADIUM‐CATALYZED HYDROGENATION APPROACH
Chandrashekar R. Elati,1 Naveenkumar Kolla,1 Subrahmanyeswara Rao Chalamala,1 Pravinchandra J. Vankawala,1 Venkataraman Sundaram,1 Himabindu Vurimidi,2 and Vijayavitthal T. Mathad1
1Department of Research and Development, Dr. Reddy's Laboratories Ltd., IPD, Unit III, Bollaram, Hyderabad 502 325, Andhra Pradesh, India
2Institute of Science and Technology, J. N. T. University, Kukatpally, Hyderabad, Andhra Pradesh, India
Abstract
Synth. Commun. 2006, 35, 175
ASYMMETRIC INDUCTION FROM ETHYL LACTATE IN THE REDUCTION OF ACETOPHENONE TO PHENYLETHANOL
Stefan H. Hüttenhain
Fachhochschule Darmstadt, Fachbereich Chemie und Biotechnologie, Hochschulstrasse 2, Darmstadt 64289, Germany
Abstract
Synth. Commun. 2006, 35, 181
PREPARATION AND CHEMICAL BEHAVIOR OF 2‐(TERT‐BUTOXYCARBONYL) AMINO‐3‐BROMOMETHYL PYRIDINE, A NOVEL ALKYLATING AGENT
Mikhail Krasavin, Sergey Shkavrov, and Dmitry Kravchenko
Chemical Diversity Research Institute, 2a Rabochaya St., Khimki, Moscow Reg., Russia
Abstract
Synth. Commun. 2006, 35, 187
FACILE PREPARATION AND PURIFICATION OF MONO TERT‐BUTYL MALONATE
Vitali I. Tararov,1 Andrei Korostylev,1 Gerd König,2 and Armin Börner1,3
1Leibniz‐Institut für Organische Katalyse e.V., A.‐Einsteinstr. 29a, 18059 Rostock, Germany
2Ratiopharm GmbH, Ulm, Germany
3Institut für Chemie der Universität Rostock, Rostock, Germany
Abstract
Synth. Commun. 2006, 35, 193
SYNTHESIS OF N‐SUBSTITUTED 4,6‐DIMETHYL‐3‐CYANO‐2‐PYRIDONES UNDER MICROWAVE IRRADIATION
Dušan Mijin and Aleksandar Marinković
Department of Organic Chemistry, Faculty of Technology and Metallurgy, University of Belgrade, 11120 Belgrade, Serbia and Montenegro
Abstract
Synth. Commun. 2006, 35, 199
FIRST HIGHLY EFFICIENT SYNTHESIS OF BIS(ARYLMETHYLIDENE) PYRANONES MEDIATED BY LITHIUM PERCHLORATE
M. Saeed Abaee, Mohammad M. Mojtahedi, M. Mehdi Zahedi, and S. Mohammad Bolourtchian
Chemistry and Chemical Engineering Research Center of Iran, P.O. Box 14335‐186 Tehran, Iran
Abstract
Synth. Commun. 2006, 35, 207
MICROWAVE‐MEDIATED DEBROMINATION OF VICINAL‐DIBROMIDES
J. M. Khurana and A. Agrawal
Department of Chemistry, University of Delhi, Delhi 110007, India
Debromination of vicinal‐dibromides to E‐alkenes is reported using inorganic solid supports (silica gel or acidic alumina) under microwave irradiation.
Abstract
Synth. Commun. 2006, 35, 211
EFFICIENT METHOD FOR SILYLATION OF P‐NITROBENZYL‐2‐DIAZOACETOACETATE
Neera Tewari, Bishwa Prakash Rai, Hashim Nizar, and Shailendra Kumar Singh
Chemical Research Division, Ranbaxy Research Laboratories, Plot No. 20, Sector‐18, Udyog Vihar Industrial Area, Gurgaon 122 001, Haryana, India
Abstract
Synth. Commun. 2006, 35, 215
SYNTHESIS AND EVALUATION OF SUBSTITUTED PYRAZOLES: POTENTIAL ANTIMALARIALS TARGETING THE ENOYL‐ACP REDUCTASE OF PLASMODIUM FALCIPARUM
Sanjay Kumar,1 Gyanendra Kumar,1 Mili Kapoor,1 Avadhesha Surolia,1 and Namita Surolia2
1Molecular Biophysics Unit, Indian Institute of Science, Bangalore, India
2Molecular Biology and Genetics Unit, Jawaharlal Nehru Center for Advanced Scientific Research, Jakkur, Bangalore 560064, India
Abstract
Synth. Commun. 2006, 35, 227
COPPER(II) BROMIDE–CATALYZED IMINO DIELS–ALDER REACTION: SYNTHESIS OF PYRANO[3,2‐C]‐ AND FURO[3,2‐C]TETRAHYDROQUINOLINES
Abha Semwal and Sandip K. Nayak
Bio‐organic Division, Bhabha Atomic Research Centre, Mumbai 400085, India
Abstract
Synth. Commun. 2006, 35, 237
FACILE METHOD FOR STEREOSELECTIVE SYNTHESIS OF NEW CHIRAL (1R,4aR,8aR)‐1,3,4,4a,5,7,8,8a‐OCTAHYDRO‐2‐METHYLENE‐NAPHTHALENE‐6‐ONE‐1‐PROPANENITRILE, AN IMPORTANT PRECURSOR OF SOLANAPYRONES
Haijian Shi
College of Chemistry and Chemical Engineering, Key Laboratory of Material‐Oriented Chemical Engineering of Jiangsu Provience, Nanjing University of Technology, Nanjing 210009, China
A short stereoselective synthesis of new precursor of solanapyrone, using one‐pot hydrogenation/acetalization and Beckmann fragmentation as the key steps, is described.
Abstract
Synth. Commun. 2006, 35, 249
ACID‐PROMOTED RING OPENING OF α‐HYDROXYL CYCLOBUTANONES: A NOVEL AND FACILE ONE‐POT SYNTHESIS OF NITRILE DERIVATIVES
Xingxian Zhang1 and Weidong Z. Li2
1College of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou, Zhejiang 310014, China
2National Laboratory of Applied Organic Chemistry and Institute of Organic Chemistry, Lanzhou University, Lanzhou, Gansu, China
A facile one‐pot synthesis of nitriles via a ring‐opening reaction of cyclobutanone adducts with hydroxylamine hydrochloride was developed.
Abstract
Synth. Commun. 2006, 35, 255
α‐CHLORINATION OF ACETOPHENONES USING 1,3‐DICHLORO‐5,5‐DIMETHYLHYDANTOIN
Zijin Xu, Deyan Zhang, and Xinzhuo Zou
Department of Chemistry, East China Normal University, 3663 Zhongshan Road (N), Shanghai 200062, China
A novel method for the synthesis of α‐chloroacetophenones using 1,3‐dichloro‐5,5‐dimethylhydantoin (DCDMH) and p‐toluenesulfonic acid in methanol at 30–35°C is described.
