✦ LIBER ✦

Efficient Synthesis of 3-Aminocyclobut-2-en-1-ones: Squaramide Surrogates as Potent VLA-4 Antagonists.

✍ Scribed by Stephen Brand; Benjamin C. de Candole; Julien A. Brown

Publisher: John Wiley and Sons
Year: 2003
Weight: 178 KB
Volume: 34
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200342076

No coin nor oath required. For personal study only.

✦ Synopsis

Abstract

For Abstract see ChemInform Abstract in Full Text.

📜 SIMILAR VOLUMES

Efficient Regioselective Three-Component

Efficient Regioselective Three-Component Domino Synthesis of 3-(1,2,4-Triazol-5-yl)-1,3-thiazolidin-4-ones as Potent Antifungal and Antituberculosis Agents

✍ Serry A. El Bialy; Maria M. Nagy; Hamdy M. Abdel-Rahman 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 178 KB 👁 2 views

Efficient Synthesis of 8-Oxabicyclo[3.2.

Efficient Synthesis of 8-Oxabicyclo[3.2.1]oct-6-en-3-ones, Preparatively Useful [4 + 3]-Cycloadducts

✍ Prof. Dr. Baldur Föhlisch; Eberhard Gehrlach; Dr. Rolf Herter 📂 Article 📅 1982 🏛 John Wiley and Sons 🌐 English ⚖ 114 KB 👁 1 views

First Synthesis of 1-Aryl-4,4-dichlorobu

First Synthesis of 1-Aryl-4,4-dichlorobut-3-en-1-ones. The Electrochemical Reduction of 1-Aryl-4,4,4-trichlorobut-2-en-1-ones as a Key Step.

✍ Antonio Guirado; Bruno Martiz; Raquel Andreu; Delia Bautista; Jesus Galvez 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 21 KB 👁 2 views

A Novel Synthesis of 7-Aryl-8-fluoro-pyr

A Novel Synthesis of 7-Aryl-8-fluoro-pyrrolo[1,2-a]pyrimid-4-ones as Potent, Stable GnRH Receptor Antagonists.

✍ Fabio C. Tucci; Yun-Fei Zhu; Zhiqiang Guo; Timothy D. Gross; Patrick J. Connors 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 126 KB 👁 2 views

Synthesis and characterization of tritiu

Synthesis and characterization of tritium labeled 2,3,4,9-tetrahydro-1H-carbazoles as potent DP receptor antagonists

✍ Carl Berthelette; Michael J. Boyd; Nicolas Lachance; Bruno Roy; Claudio F. Sturi 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 French ⚖ 109 KB

## Abstract Tritium labeled 2,3,4,9‐tetrahydro‐1__H__‐carbazole **1a** and **2a** were prepared in good yields with a specific activity of 7.0 Ci/mmol (214 GBq/mmol) and 4.2 Ci/mmol (155 GBq/mmol), respectively. Both compounds have been synthesized in high radiochemical purity by catalytic tritium–

ChemInform Abstract: Synthesis and Biolo

ChemInform Abstract: Synthesis and Biological Evaluation of 1,2,3,4-Tetrahydroisoquinoline Derivatives as Potent and Selective M2 Muscarinic Receptor Antagonists.

✍ Toshihiro Watanabe; Isao Kinoyama; Kenji Takizawa; Seiko Hirano; Tadao Shibanuma 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 1 views