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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 37, 2007 - Issue 21
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Abstracts

Graphical Abstracts

Pages 3689-3696 | Published online: 19 Oct 2007
 

Abstract

Graphical Abstract Section

Abstract

Synth. Commun. 2007, 37, 3697

SYNTHETIC ACCESS TO NEW PYRIDONE DERIVATIVES THROUGH THE ALKYLATION REACTIONS OF HYDROXYPYRIDINES WITH EPOXIDES

Ahmet Kocak, Sultan Kurbanli, and Sait Malkondu

Faculty of Science and Arts, Department of Chemistry, University of Selcuk, Konya, Turkey

Abstract

Synth. Commun. 2007, 37, 3709

NEW CONVENIENT REAGENTS FOR CHEMOSELECTIVE N-ALKOXYCARBONYLATION OF (S)-ISOSERINE: APPLICATION IN the ISEPAMICIN SYNTHESIS

Konstantin Doktorov, Velichko Tarpanov, and Pepa Mechkarova

Institute of Organic Chemistry with Centre of Phytochemistry, Bulgarian Academy of Science, Sofia, Bulgaria

Abstract

Synth. Commun. 2007, 37, 3719

NOVEL METHOD FOR THE SYNTHESIS OF [1,2,4]TRIAZINO[4,3-C]QUINAZOLINE SYSTEM

Sergey I. Kovalenko,1 Alexander V. Karpenko,1 Oksana V. Krivoshey,1 Svetlana V. Shishkina,2 and Oleg V. Shishkin2

1Department of Pharmaceutical Chemistry, Zaporozhye State Medical University, Zaporozhye, Ukraine

2STC Institute for Single Crystals, National Academy of Sciences of Ukraine, Kharkov, Ukraine

Abstract

Synth. Commun. 2007, 37, 3729

STUDIES ON THE SELECTIVE REDUCTION OF THE AMIDE LINK OF ACYCLIC AND MACROCYCLIC AMIDOKETALS: UNEXPECTED CLEAVAGE AND TRANS-ACETALIZATION WITH RED-AL®

Radouane Affani and Denise Dugat

Laboratoire SEESIB (Synthèse et Etude de Systèmes à Intérêt Biologique), Université Blaise Pascal de Clermont-Ferrand, Aubière, France

Abstract

Synth. Commun. 2007, 37, 3741

Novel Atom-Economic Nitration of Benzene with a Nitrogen Dioxide–Oxygen System using Cocatalyst of Solid Oxides and Lanthanide(III) Metal Triflates

Xiaohua Du, Xiaoqing Li, and Zhenyuan Xu

State Key Laboratory Breeding Base of Green Chemistry–Synthesis Technology, Zhejiang University of Technology, Hangzhou, China

Abstract

Synth. Commun. 2007, 37, 3751

SAMARIUM TRIIODIDE–CATALYZED FORMATION OF MANNICH-TYPE PRODUCTS BY AMIDOALKYLATION OF 1,3-DICARBONYL COMPOUNDS

Xiaoxia Wang, Hui Mao, Yan yu, Xiudan Zhu, and Chunlan Zhu

Zhejiang Key Labortary for Reactive Chemistry on Solid Surfaces, College of Chemistry and Life Scienes, Zhejiang Normal University, Jinhua, China

Abstract

Synth. Commun. 2007, 37, 3759

Convenient Synthesis of Aryl Ferrocenyl Ketone via Palladium‐Catalyzed Carbonylation Coupling

Dong Yang,1 Zenglu Liu,2 Ying Li,1 and Baohua Chen1

1State Key Laboratory of Applied Organic Chemistry, Lanzhou University China, Lanzhou, China

2Pharmacy College of Shanghai Jiao Tong University, Shanghai, China

Abstract

Synth. Commun. 2007, 37, 3767

Efficient One-pot Synthesis of 2-Amino-4,6-diarylbenzene-1,3-dicarbonitrile under Solvent-free Conditions

Liangce Rong,1,2 Hongxia Han,1 Fang Yang,1 Hao Yao,1 Hong Jiang,2 and Shujiang Tu,1,2

1Department of Chemistry, Xuzhou Normal Univeristy, Xuzhou, Jiang Su, China

2Key laboratory of Biotechnology for Medicinal Plant, Xuzhou, Jiangsu, China

A facile parallel synthesis of 2-amino-4,6-diarylbenzene-1,3-dicarbonitrile derivatives via one-pot reaction of aromatic aldehydes, aromatic ketone, malononitrile under solvent-free conditions has been developed. This new protocol has the advantages of shorter time, higher yields, lower cost, and environmental friendliness.

Abstract

Synth. Commun. 2007, 37, 3773

Novel Synthetic Route of (2S)‐6‐Fluoro‐4‐oxo‐3,4‐dihydro‐2H‐chromene‐2‐carboxylic Acid

Hua-Jie Yuan, Shan Quian, Li Hai, Yao-Yao Chen, and Yong Wu

Key Laboratary of Drug Targeting of Education Ministry, West China School of Pharmacy, Sichuan University, Chengdu, Sichuan, China

(2S)‐6‐Fluoro‐4‐oxo‐3,4‐dihydro‐2H‐chromene‐2‐carboxylic acid, a key intermediate of Fidarestat, was synthesized from natural chiral pool D‐mannitol.

Abstract

Synth. Commun. 2007, 37, 3779

Synthesis biological evaluation of new 4-deacety-1,7,9-trideoxy-10-oco paclitaxel via sinenxan A

Huixia Du,1 Meng Zhang,1 Dali Yin,1 Yan Li,2 and Xiaoguang Chen2

Abstract

Department of Medicinal Chemistry, Institute of Materia Medica, Peking Union Medical College and Chinese Academy of Medical Science, Beijing, China

Department of Pharmacology, Institute of Materia Medica, Peking Union Medical College and Chinese Academy of Medical Science, Beijing, China

A new 1,7,9-trideoxy-4-deacety-10-oxopaclitaxel (1) was synthesized in 21 steps via sinenxan A and evaluated in vitro for cytotoxicity against human cancer cell lines.

Abstract

Synth. Commun. 2007, 37, 3793

Practical Synthesis Of Structurally Important Spirodiamine Templates

Fei‐Yu Tang, Li‐Qiang Qu, Yan Xu, Ru‐Jian Ma, Shu‐Hui Chen, and Ge Li

A general, concise four‐step synthetic sequence for the preparation of the spiro‐diamine templates is described herein.

Abstract

Synth. Commun. 2007, 37, 3801

Unexpected Rearrangement in the Reaction of 7-Mercapto-4-methylcoumarin with 1-Mono- and 1,1-Dimethyl Propargyl Alcohols

Shiqing Xu, Xin Yan, Qian Zhang, Peng Xia, and Ying Chen

Department of Medicinal Chemistry, School of Pharmacy, Fudan University, Shanghai, China The reaction of 7-mercapo-4-methylcoumarin (4) with 1-mono- and 1,1-dimethyl propargyl alcohols in H3PO4 afforded the corresponding β-(7-coumarinthio)ketones with a rearrangement of the carbon chain of propargyl.

Abstract

Synth. Commun. 2007, 37, 3809

PALLADIUM-CATALYZED KUMADA REACTION EMPLOYING AMINOPHOSPHINE AS LIGAND

Lin Zhang, Jiang Cheng, Weiwei Zhang, Baoda Lin, Changduo Pan, and Jing Chen

College of Chemistry and Material Engineering, Wenzhou University, Wenzhou, China

Abstract

Synth. Commun. 2007, 37, 3815

SYNTHESIS OF 3-ARYL-5-T-BUTYLSALICYLALDEHYDES AND THEIR CHIRAL SCHIFF BASE COMPOUNDS

Hai-Bin Liu,1 Mei Wang,1 Ying Wang,1 Qiang Gu,1 and Li-Cheng Sun1,2

1State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian, Liaoning, China

2School of Chemical Science and Engineering, Royal Institute of Technology, Stockholm, Sweden

Abstract

Synth. Commun. 2007, 37, 3827

YTTERBIUM PERFLUOROOCTANESULFONATE CATALYZED SYNTHESIS OF 1,5-BENZODIAZEPINE DERIVATIVES IN FLUOROUS SOLVENTS

Wen-Bin Yi and Chun Cai

Chemical Engineering College, Nanjing University of Science and Technology, Nanjing, China

Abstract

Synth. Commun. 2007, 37, 3835

Solid-State Photodimerization of 1,2-bis(5′-Pyrimidyl)ethene

Eric Bosch,1 Julie M. Matheny,1 and Nigam Rath2

1Depatment of Chemistry, Missouri State University, Springfield, Missouri, USA

2Department of Chemistry, University of Missouri, St. Louis, Missouri, USA

Abstract

Synth. Commun. 2007, 37, 3841

NEW PHOSPHONATE REAGENTS FOR ALDEHYDE HOMOLOGATION

Richard J. Petroski

United States Department of Agriculture, Agricultural Research Service, National Center for Agricultural Utilization Research, Crop Bioprotection Research Unit, Peoria, Illinois, USA Using these reagents led to a two-step aldehyde homologation cycle (condensation and deprotection), and overall yields ranged from 71% to 84%.

Abstract

Synth. Commun. 2007, 37, 3855

COMPARISON OF IODINATION OF METHOXYLATED BENZALDEHYDES AND RELATED COMPOUNDS USING IODINE/SILVER NITRATE AND IODINE/PERIODIC ACID

Bruce A. Hathaway, Kristen L. White, and Mark E. McGill

Department of Chemistry, Southeast Missouri State University, Cape Girardeau, Missouri, USA

Abstract

Synth. Commun. 2007, 37, 3861

Synthesis and characterization of novel quaternary ammonium RAFT agents

Austin Samakande, Ronald D. Sanderson, and Patrice C. Hartmann

UNESCO Associated Centre for Macromolecules, Department of Chemistry and Polymer Science, Univrsity of Stellenbosch, Matieland, South Africa

Abstract

Synth. Commun. 2007, 37, 3873

Convenient Synthesis of Tributylsilyl Methacrylate

David Mancardi,1 Michèle Sindt,1 Jean‐Michel Paul,2 and Jean‐Luc Mieloszynski1

1Laboratory of Chemistry and Methodology for the Environment (LCME), Paul Verlaine‐Metz University, Metz, France 2Arkema, Research and Development Centre (CRDE), Saint Avold, France

Abstract

Synth. Commun. 2007, 37, 3879

New Access to Organoacyloxytrialkylsilanes

David Mancardi,1 Michèle Sindt,1 Jean‐Michel Paul,2 and Jean‐Luc Mieloszynski1

1Laboratory of Chemistry and Methodology for the Environment (LCME), Paul Verlaine‐Metz University, Metz, France 2Arkema, Research and Development Centre (CRDE), Saint Avold, France

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