Abstract
Graphical Abstract Section
Abstract
Synth. Commun. 2006, 35, 1147
OXONE/SODIUM CHLORIDE: A SIMPLE AND EFFICIENT CATALYTIC SYSTEM FOR THE OXIDATION OF ALCOHOLS TO SYMMETRIC ESTERS AND KETONES
Agnes Schulze, Georgia Pagona, and Athanassios Giannis
Institut für Organische Chemie, Universität Leipzig, Leipzig, Germany
Abstract
Synth. Commun. 2006, 35, 1157
STEREOCONTROLLED TRANSFORMATIONS OF TRANS α,β‐AZIRIDINE ALDEHYDES TOWARD DIFFERENT AMINO HYDROXYLATED STRUCTURES
Giuliana Righi,1 Simona Ciambrone,1 and Carlo Bonini2
1Istituto di Chimica Biomolecolare‐Sezione di Roma, c/o Dipartimento di Chimica, Università “La Sapienza,” Roma, Italy
2Dipartimento di Chimica, Università della Basilicata, Potenza, Italy
Abstract
Synth. Commun. 2006, 35, 1167
INFLUENCE OF CARBOXYLIC ACIDS ON THE SYNTHESIS OF CHLOROHYDRIN ESTERS FROM 1,3‐BUTANEDIOL
Jonh Jairo Méndez,1,3 Jordi Eras,1 Mercè Balcells,2 and Ramon Canela2
1Chemistry Department, Universitat de Lleida, Lleida, Spain
2Chemistry Department and Centre UdL‐IRTA, Universitat de Lleida, Lleida, Spain
3Chemistry Department, Tolima University, Colombia
The influence of the carboxylic acid on the preparation of chlorohydrin esters using a one‐pot esterification–chlorination reaction, in which one of the reagents (chlorotrimethylsilane) acts as solvent, is described. The pKa of each acid has a clear influence on the regioisomeric rate.
Abstract
Synth. Commun. 2006, 35, 1177
FACILE AND VERSATILE ROUTE TO THE SYNTHESIS OF FUSED 2‐PYRIDONES: USEFUL INTERMEDIATES FOR POLYCYCLIC SYTEMS
Barbara Cacciari1 and Giampiero Spalluto2
1Dipartimento di Scienze Farmaceutiche, Università degli Studi di Ferrara, Ferrara, Italy
2Dipartimento di Scienze Farmaceutiche, Università degli Studi di Trieste, Trieste, Italy
Abstract
Synth. Commun. 2006, 35, 1185
FACILE SYNTHESIS OF 2‐ALKYLTHIO‐3‐ALKYL‐5‐PHENYLMETHYLIDENE‐4H‐IMIDAZOL‐4‐ONES
Yong Sun,1 Li‐Ping Gao,1 and Ming‐Wu Ding2
1Department of Chemistry, Yunyang Teachers College, Danjiangkou, China
2Institute of Organic Synthesis, College of Chemistry, Central China Normal University, Wuhan, China
Abstract
Synth. Commun. 2006, 35, 1193
SEQUENTIAL ALDOL/MICHAEL ADDITION REACTION IN IONIC LIQUID CATALYZED BY MORPHOLINE: A CONVENIENT SYNTHESIS OF 1,3,5‐TRIARYL‐1,5‐PENTANEDIONE
Hui Wu,1,2 Leilei Lu,1 Yang Shen,1 Yu Wan,1 and Kaibei Yu3
1Department of Chemistry, Xuzhou Normal University, Xuzhou, Jiangsu, China
2Key Laboratory of Biotechnology on Medical Plants of Jiangsu Province, Xuzhou, Jiangsu, China
3Chengdu Institute of Organic Chemistry, Chinese Academy of Sciences, Chengdu, Sichuan, China
Abstract
Synth. Commun. 2006, 35, 1201
REGIOSELECTIVE SYNTHESIS OF 6‐PRENYLPOLYHYDROXYISOFLAVONE (WIGHTEONE) AND WIGHTEONE HYDRATE WITH HYPERVALENT IODINE
Mohammad M. Hossain, Takanori Tokuoka, Kazuyo Yamashita, Yasuhiko Kawamura, and Masao Tsukayama
Department of Chemical Science and Technology, Faculty of Engineering, University of Tokushima, Tokushima, Japan
The oxidative rearrangement of 3′‐iodochalcone with HTIB, followed by cyclization of the resulting acetal, gave 6‐iodoisoflavone. Wighteone was synthesized by dehydration of wighteone hydrate, prepared by the coupling of the isoflavone and hydrogenation.
Abstract
Synth. Commun. 2006, 35, 1213
SIMPLE SYNTHESIS OF GEMINAL DIACETATES (ACYLALS) OF AROMATIC ALDEHYDES
Motiur A. F. M. Rahman and Yurngdong Jahng
College of Pharmacy, Yeungnam University, Gyongsan, Korea
The geminal diacetates of aromatic aldehydes were readily prepared from corresponding aldehydes by refluxing with acetic anhydride without any catalysts or even any additional solvent.
Abstract
Synth. Commun. 2006, 35, 1221
RAPID AND EFFICIENT METHOD FOR ACETYLATION OF ALCOHOLS AND PHENOLS WITH ACETIC ANHYDRIDE CATALYZED BY SILICA SULFATE
Tong‐Shou Jin, Ying Zhao, Li‐Bin Liu, Zhuo Chen, and Tong‐Shuang Li
Department of Chemistry, College of Chemistry and Environmental Science, Hebei University, Baoding, China
A rapid and efficient method is described for acetylation of a series of alcohols and phenols with acetic anhydride catalyzed by silica sulfate solid acid at room temperature or at refluxing temperature in excellent yield.
Abstract
Synth. Commun. 2006, 35, 1229
ONE‐POT SYNTHESIS OF 5‐ALKYLFURAN‐2(5H)‐ONES
Jie Ma, Si Hong Wang, and Guan Rong Tian
Department of Chemistry, Yanbian University, Yan Ji, Ji Lin, China
Abstract
Synth. Commun. 2006, 35, 1235
METHYL, TRIFLUOROMETHYL, AND METHOXYCARBONYL—INTRODUCTION TO THE FIFTH POSITION ON THE PYRIDINE RING OF CHLORONICOTINYL INSECTICIDE IMIDACLOPRID
Shinzo Kagabu
Department of Chemistry, Faculty of Education, Gifu University, Gifu, Japan
Three substituted derivatives of the potent insecticide imidacloprid were prepared.
Abstract
Synth. Commun. 2006, 35, 1247
PALLADIUM(II)‐CATALYZED SYNTHESIS OF ISOXAZOLIDINES: USING A CATALYTIC COPPER ACETATE AND MOLECULAR OXYGEN AS THE COOXIDANT
Krishna Gopal Dongol,1 Boon Ying Tay,1 Kai Xiang,2 and Thies Thiemann2
1Institute of Chemical and Engineering Sciences, Jurong Island, Singapore
2Institute of Material Chemistry and Engineering, Kyushu University, Kasuga Koh-en, Kasuga-shi, Japan
An efficient and environmentally friendly process is reported for the palladium(II)‐catalyzed cyclofunctionalization of allylic hydroxylamine derivatives using oxygen as the cooxidant with only a catalytic amount of copper(II) acetate is reported. This method shows the environmentally benign process for the synthesis of isoxazolidine derivatives.
Abstract
Synth. Commun. 2006, 35, 1259
ALCL3·6H2O/KI/CH3CN/H2O: AN EFFICIENT AND VERSATILE SYSTEM FOR CHEMOSELECTIVE C–O BOND CLEAVAGE AND FORMATION OF HALIDES AND CARBONYL COMPOUNDS FROM ALCOHOLS IN HYDRATED MEDIA
Pranjal Gogoi,1 Dilip Konwar,1 Saikat Das Sharma,1 and Prodip Kumar Gogoi2
1Organic Chemistry Division, Regional Research Laboratory, Jorhat, Assam, India
2Department of Chemistry, Dibrugarh University, Dibrugarh, Assam, India
Abstract
Synth. Commun. 2006, 35, 1273
SYNTHESIS OF SUBSTITUTED TRICYCLO[5.3.1.04,9]UNDECAN‐2,6‐DIONE FROM 4,4‐DISUBSTITUTED CYCLOHEXANONE ENAMINES AND METHACRYLOYL CHLORIDE
M. Giasuddin Ahmed,1 Syeda Asghari Ahmed,1 Kawsari Akhter,1 Yoshisuke Tsuda,2 M. Mahmun Hossain,3 and F. Holger Forsterling3
1Department of Chemistry, University of Dhaka, Dhaka, Bangladesh
2Faculty of Pharmaceutical Sciences, Kanazawa University, Kanazawa, Japan
3Department of Chemistry, University of Wisconsin—Milwaukee, Milwaukee, Wisconsin, USA
Abstract
Synth. Commun. 2006, 35, 1291
STUDIES ON AMINE OXIDE REARRANGEMENT: SYNTHESIS OF PYRROLO[3,2‐C][1]BENZOTHIOPYRAN‐4‐ONE
K. C. Majumdar, S. K. Chattopadhyay, and P. P. Mukhopadhyay
Department of Chemistry, University of Kalyani, Kalyani, West Bengal, India
Abstract
Synth. Commun. 2006, 35, 1299
SEQUENTIAL [3,3]SIGMATROPIC REARRANGEMENT: REGIOSELECTIVE SYNTHESIS OF DIMEDONE‐ANNULATED HETEROCYCLES
K. C. Majumdar and S. K. Samanta
Department of Chemistry, University of Kalyani, Kalyani, India
Abstract
Synth. Commun. 2006, 35, 1307
COPPER(II) BROMIDE–CATALYZED CONJUGATE ADDITION OF INDOLES TO α,β‐ENONES
Sandip K. Nayak
Bio‐organic Division, Bhabha Atomic Research Centre, Mumbai, India