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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 37, 2007 - Issue 3
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Abstracts

Graphical Abstracts

Pages 353-359 | Published online: 06 Feb 2007
 

Abstract

Graphical Abstract Section

Abstract

Synth. Commun. 2007, 37, 361

FACILE TOTAL SYNTHESIS OF XANTHOTOXOL

Wei He,1 Bang-Le Zhang,2 Si-Yuan Zhou,2 Xiao-Li Sun,1 Sheng-Yong Zhang1

1Department of Chemistry, Fourth Military Medical University, Xi'an, Shaanxi, China

2Department of Pharmacology, Fourth Military Medical University, Xi'an, Shaanxi, China

Abstract

Synth. Commun. 2007, 37, 369

IMPROVED SYNTHESIS OF 2-(3H)BENZOTHIAZOLETHIONES UNDER MICROWAVE IRRADIATION

Wei Huang, Ying Tan, Ming-Wu Ding, and Guang-Fu Yang

Key Laboratory of Pesticide & Chemical Biology, Ministry of Education, College of Chemistry, Central China Normal University, Wuhan, China

Abstract

Synth. Commun. 2007, 37, 377

REACTION OF IMIDAZO[1,2-A]PYRIDINES WITH ALIPHATIC ALDEHYDES: A SIMPLE AND EFFICIENT METHOD FOR THE PREPARATION OF NOVEL C-3 VINYLIC DERIVATIVES OF IMIDAZO[1,2-A]PYRIDINES

Rui Zhang and Yongzhou Hu

Ecole Normal Superieure Joint Laboratory of Medicinal Chemistry, School of Pharmaceutical Sciences, Zhejiang University, Zijingang Campus, Hangzhou, P.R. China

A number of C-3 vinylic derivatives of imidazo[1,2-a]pyridines were synthesized by the reaction of imidazo[1,2-a]pyridines with different aliphatic aldehydes in mild to good yields.

Abstract

Synth. Commun. 2007, 37, 391

NOVEL PROCEDURE FOR HIGHLY STEREOSELECTIVE SYNTHESIS OF BICYCLIC CYCLOPROPANE-LACTAM WITH CIS-2-ARYL-1-BENZOYL-3,3-DICYANOCYCLOPROPANE AND 2-CYANOMETHYL-1,3-BENZOTHIAZOLE IN WATER

Zhongjiao Ren,1 Weiguo Cao,1,2 Jie Chen,1 and Yeying Lu1

1Department of Chemistry, Shanghai University, Shanghai, China

2State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai, China

The novel procedure for synthesis of cyclopropyl lactams incorporating benzothiazole structure unit via reaction of cis-2-aryl-1-benzoyl-3,3-dicynocyclopropane and 2-cyanomethyl-1,3-benzothiazole has been achieved.

Abstract

Synth. Commun. 2007, 37, 399

UNEXPECTED MICROWAVE REACTION OF 1,3-DISUBSTITUTED IMIDAZOLIUM SALTS: A NOVEL SYNTHESIS OF 1,3-DISUBSTITUTED IMIDAZOLE-2-THIONES

Xiao-Le Tao, Ming Lei, and Yan-Guang Wang

Department of Chemistry, Zhejiang University, Hangzhou, Zhejiang, China

A microwave-promoted reaction of 1,3-disubstituted imidazolium salts with potassium thioacetate or potassium thiocyanate under solvent-free conditions provided a rapid and efficient synthesis of 1,3-disubstituted imidazole-2-thiones.

Abstract

Synth. Commun. 2007, 37, 409

SIMPLE AND CONVENIENT SYNTHESIS OF 21-THIOALKYLETHER DERIVATIVES OF METHYL 16-PREDNISOLONE CARBOXYLATES

M. Omar F. Khan and Henry J. Lee

College of Pharmacy and Pharmaceutical Sciences, Florida A & M University, Tallahassee, Florida, USA

21-Mesylate of methyl-16-perdnisolonecarboxylate and 9-fluoro-17-dehydro methyl 16-prednisolonecarboxylate were reacted with Na-thioalkoxides to furnish corresponding 21-thioethers.

Abstract

Synth. Commun. 2007, 37, 417

HYDROGENATION OF IMINO-BISNITRILES—SYNTHESIS OF NOVEL TRIAMINES

Raji Sundaramoorthi and Terence P. Keenan

ARIAD Pharmaceuticals Inc., Cambridge, Massachasetts, USA

The hydrogenation of iminonitriles and iminobisnitriles of type 1af is a particularly difficult process as the intermediate dieneamines are highly susceptible to addition reactions. A short general method of preparation and purification of 2-aminomethylene-1,3-diamine of type 2ae by catalytic hydrogenation of iminobisnitriles is described.

Abstract

Synth. Commun. 2007, 37, 425

FACILE SYNTHESIS OF ISODAMASCONE AND ITS ANALOGS

Dinesh W. Rangnekar,1 Vikas S. Kulkarni,1 Prasad V. Ranade,1 and Ram W. Sabnis2

1Dyes Research Laboratory, Institute of Chemical Technology, University of Mumbai, Matunga, Mumbai, India2Ascadia Inc., Eagan, Minnesota, USA

Synthesis of isodamascone and its analogs, the commercially important aroma compounds, have been accomplished from the readily available 1,5,5-trimethyl-2-cyclohexen-1-ol via a short, facile, and simple sequence of reactions in excellent yield.

Abstract

Synth. Commun. 2007, 37, 431

APPLICATION OF POLYMER-SUPPORTED TRIPHENYLPHOSPHINE AND MICROWAVE IRRADIATION TO THE PALLADIUM-CATALYZED CYANATION OF ARYL TRIFLATES

Rajiv R. Srivastava, Andrew J. Zych, David M. Jenkins, Hong-Jun Wang, Zhen-Jia Chen, and David J. Fairfax

Department of Medicinal Chemistry, Albany Molecular Research, Inc., Albany, NY, USA.

Abstract

Synth. Commun. 2007, 37, 439

SYNTHESIS OF IPRATROPIUM BROMIDE–RELATED COMPOUNDS

Irina Tsyskovskaia, Mustapha Kandil, and Yves Beaumier

Pharmascience Inc., Saint-Laurent, Quebec, Canada

Abstract

Synth. Commun. 2007, 37, 447

SYNTHESIS OF A NEW DOXAZOSIN-RELATED COMPOUND

Irina Tsyskovskaia, Mustapha Kandil, and Yves Beaumier

Pharmascience, Saint-Laurent, Quebec, Canada

Abstract

Synth. Commun. 2007, 37, 451

SYNTHESIS OF A NOVEL DISPIROHETEROCYCLIC FRAMEWORK VIA THE REGIOSELECTIVE 1,3-DIPOLAR CYCLOADDITION REACTION OF AZOMETHINE YLIDES

A. R. Suresh Babu and R. Raghunathan

Department of Organic Chemistry, University of Madras, Chennai, India

Abstract

Synth. Commun. 2007, 37, 459

NEW SYNTHESIS OF 2-POLYHFLUOROALKYL SUBSTITUTED 1,4,5,6-TETRAHYDRO-PYRIMIDINES AND 4,5,6,7-TETRAHYDRO-1H-1,3-DIAZEPINES

Alexander V. Rudnichenko and Yuriy G. Shermolovich

Institute of Organic Chemistry, NAS of Ukraine, Kyiv, Ukraine

Abstract

Synth. Commun. 2007, 37, 467

NOVEL ROUTE TO 2-ARYLAPOMORPHINES

Sándor Berényi,1 Attila Sipos,1 Ildikó Szabó,1 and Tamás Kálai2

1Department of Organic Chemistry, University of Debrecen, Debrecen, Hungary

2Institute of Organic and Medicinal Chemistry, University of Pécs, Pécs, Hungary

The synthesis of 2-arylapomorphines (1, 2) has been accomplished using a new method involving a Suzuki-type cross-coupling reaction of 2-bromoapocodeine (8) and arylboronic acids.

Abstract

Synth. Commun. 2007, 37, 473

A NEW FERROCENE-CONTAINING POLYAMIDE PREPARED FROM AN IMPROVED SYNTHESIS OF 1,1′-FERROCENE DICARBONYL CHLORIDE AND FERROCENE-BASED DIAMINE

Muhammad Saif ullah Khan, Asifa Nigar, Mubashir A. Bashir, and Zareen Akhter

Department of Chemistry, Quaid-i-Azam University, Islamabad, Pakistan

Abstract

Synth. Commun. 2007, 37, 483

PREPARATION OF MONOALKYL TEREPHTHALATES: AN OVERVIEW

Elodie-Denise Chenot,1 Dan Bernardi,2 Alain Comel1, and Gilbert Kirsch1

1Laboratoire d'Ingénierie Moléculaire et Biochimie Pharmacologique (LIMBP), Université Paul Verlaine Metz, Metz, France

2Institut de Chimie Organique et Analytique, Université d'Orléans, Orléans, France

This article describes a simple method to convert terephthalic acid into a monoalkyl terephthalate 2 via momohydrolysis of the dialkyl terephthalate 1.

Abstract

Synth. Commun. 2007, 37, 491

ONE‐POT, THREE‐COMPONENT CONDENSATION REACTION IN WATER: AN EFFICIENT AND IMPROVED PROCEDURE FOR THE SYNTHESIS OF PYRAN ANNULATED HETEROCYCLIC SYSTEMS

Ahmad Shaabani, Sima Samadi, and Abbas Rahmati

Department of Chemistry, Shahid Beheshti University, Tehran, Iran.

Abstract

Synth. Commun. 2007, 37, 501

VERSATILE CYCLIZATION OF AMINOANILINO LACTONES: ACCESS TO BENZOTRIAZOLES AND CONDENSED BENZODIAZEPIN-2-THIONES

Lamouri Hammal,1 Samia Bouzroura,1 Chantal André,2 Bellara Nedjar-Kolli,1 and Pascal Hoffmann2

1University of Sciences and Technology Houari Boumediene, Alger, Algeria

2Paul Sabatier University, Toulouse, France

Abstract

Synth. Commun. 2007, 37, 513

SILICA-SUPPORTED BIS (TRIMETHYLSILYL) CHROMATE: OXIDATION OF THIOLS TO THEIR CORRESPONDING DISULFIDES

Majid M. Heavi,1 Fatemeh Derikvanand,1 Hossein A. Oskooie,1 Rahim Hekmat Shoar,1 and Mahmood Tajbakhsh2

1Department of Chemistry, School of Sciences, Azzahra University, Vanak, Tehran, Iran

2Department of Chemistry, Mazandaran University, Babolsar, Iran

An efficient and convenient method for the oxidation of thiols mediated by silica-supported bis (trimethylisilyl) chromate (BTSC) in acetonitrile is reported.

Abstract

Synth. Commun. 2007, 37, 519

NEW ROUTE FOR CONVERSION OF CAMPTOTHECIN TO 7-ETHYLCAMPTOTHECIN AND 7-PROPYLCAMPTOTHECIN

Xin Wang1, Xiaojing Wu2, Ning Cheng2, Huiqing Zhao1, Zhihong Gu1, and Xiang Shen3

1Department of Chemistry, College of Basic Medicine, Anhui Medical University, Hefei, Anhui, China

2School of Chemical Engineering, Hefei University of Technology, Hefei, Anhui, China

3First Affiliated Hospital, Anhui Medical University, Hefei, Anhui, China

In this article, a new route for conversion of camptothecin to 7-ethylcamptothecin and 7-propylcamptothecin is described. Compared with previous reports, the reaction time of the new synthetic route was greatly shortened to 30 min, and the products were obtained in high yield.

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