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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 36, 2006 - Issue 9
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Abstracts

Graphical Abstracts

Pages i-vi | Published online: 24 Feb 2007
 

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

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