✦ LIBER ✦

Theoretical Study of the [2+3] Cycloaddition of Nitrones to Nitriles—Influence of Nitrile Substituent, Solvent and Lewis Acid Coordination

✍ Scribed by Gabriele Wagner

Publisher: John Wiley and Sons
Year: 2003
Tongue: English
Weight: 241 KB
Volume: 9
Category: Article
ISSN: 0947-6539
DOI: 10.1002/chem.200390172

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

1,3-Dipolar Cycloaddition of Nitrones to

1,3-Dipolar Cycloaddition of Nitrones to Free and Coordinated Nitriles: Routes to Control the Synthesis of 2,3-Dihydro-1,2,4-oxadiazoles

✍ N. A. Bokach; V. Yu. Kukushkin 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 18 KB 👁 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.

Theoretical Study of 1,3-Dipolar Cycload

Theoretical Study of 1,3-Dipolar Cycloaddition Reactions with Inverse Electron Demand − A DFT Study of the Lewis Acid Catalyst and Solvent Effects in the Reaction of Nitrones with Vinyl Ethers

✍ Luis R. Domingo 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 373 KB 👁 2 views

ChemInform Abstract: Experimental and Th

ChemInform Abstract: Experimental and Theoretical Study of the 1,3-Dipolar Cycloaddition Between D-Glyceraldehyde Nitrones and Acrylates. Diastereoselective Approach to 4-Hydroxy Pyroglutamic Acid Derivatives.

✍ Pedro Merino; Juan A. Mates; Julia Revuelta; Tomas Tejero; Ugo Chiacchio; Giovan 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 1 views