✦ LIBER ✦

Microwave-assisted highly diastereoselective synthesis of oxazolidines derived from ketones and aminoalcohols

✍ Scribed by Philip C. Bulman Page; Genna A. Parkes; Benjamin R. Buckley; Harry Heaney; Mostafa Gholizadeh; J. Steven Wailes

Book ID: 104095834
Publisher: Elsevier Science
Year: 2008
Tongue: French
Weight: 171 KB
Volume: 49
Category: Article
ISSN: 0040-4039
DOI: 10.1016/j.tetlet.2008.09.063

No coin nor oath required. For personal study only.

✦ Synopsis

A number of oxazolidines derived from ketones and aminoalcohols have been prepared in excellent yields using microwave irradiation. In most cases, conventional reflux failed to provide any of the desired products.

📜 SIMILAR VOLUMES

ChemInform Abstract: Microwave-Assisted

ChemInform Abstract: Microwave-Assisted Highly Diastereoselective Synthesis of Oxazolidines Derived from Ketones and Amino Alcohols.

✍ Philip C. Bulman Page; Genna A. Parkes; Benjamin R. Buckley; Harry Heaney; Mosta 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 36 KB 👁 1 views

The Highly Diastereoselective Synthesis

The Highly Diastereoselective Synthesis of Oxazolidines Derived from Ketones and Pseudoephedrine or Ephedrine.

✍ Philip C. Bulman Page; et al. et al. 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 24 KB

Oxazolidine Sulfur Ylides Derived from P

Oxazolidine Sulfur Ylides Derived from Phenylglycinol for the Specific and Highly Diastereoselective Synthesis of Aryl and Alkyl trans -Epoxyamides

✍ Gordillo, Paola G.; Aparicio, David M.; Flores, Marcos; Mendoza, Angel; Orea, La 📂 Article 📅 2013 🏛 John Wiley and Sons 🌐 English ⚖ 504 KB

Microwave-assisted synthesis of 1,3-benz

Microwave-assisted synthesis of 1,3-benzodioxole derivatives from catechol and ketones or aldehydes

✍ Subramanya R.K. Pingali; Branko S. Jursic 📂 Article 📅 2011 🏛 Elsevier Science 🌐 French ⚖ 551 KB

An efficient synthetic procedure for the preparation of a diverse library of 1,3-benzodioxoles was developed by applying controlled microwave heating in comparison with currently available conventional heating. Reactions were completed in less than 3 h. The isolation of product is simple, the isolat

Highly diastereoselective synthesis of n

Highly diastereoselective synthesis of new optically active aminoalcohols in one step from (+)-camphor and (−)-fenchone

✍ Miroslav Genov; Kalina Kostova; Vladimir Dimitrov 📂 Article 📅 1997 🏛 Elsevier Science 🌐 English ⚖ 512 KB

New optically active aminoalcohols have been prepared from CeCl3-activated (+)-camphor and (-)-fenchone and N-functionalized organolithium compounds. The aminoalcohols obtained catalyze the addition of diethylzinc to benzaldehyde in high yields and enantioselectivities up to 64%. (~) 1997 Elsevier S

Regioselective Microwave-Assisted Synthe

Regioselective Microwave-Assisted Synthesis of Substituted Pyrazoles from Ethynyl Ketones.

✍ Mark C. Bagley; M. Caterina Lubinu; Christopher Mason 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 25 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.