Practical reduction of oxazolines to alcohols

Tetrahedron Letters

Volumn 49, Issue 47, 2008, Pages 6707-6708

  Bernardi, Anna ^a   Ouellet, Stéphane G ^a   Angelaud, Remy ^a   O'Shea, Paul D ^a  

^a MERCK FROSST CENTRE FOR THERAPEUTIC RESEARCH   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

1,1,1 TRICHLOROETHANE; ALCOHOL DERIVATIVE; LITHIUM; OXAZOLINE DERIVATIVE; SODIUM BOROHYDRIDE;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; ELECTRON; LITHIATION; METHODOLOGY; ONE POT SYNTHESIS; REDUCTION KINETICS;

EID: 53149147364     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.09.061     Document Type: Article

References (10)

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2. For recent examples, see:. Wanbin Z., Fang X., Shigeaki M., Yuji I., Toshiyuki K., Yohji N., and Isao I. Tetrahedron: Asymmetry 17 (2006) 767-777
3. For recent examples, see:. Oi S., Aizawa E., Ogino Y., and Inoue Y. J. Org. Chem. 70 (2005) 3113-3119
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5. Meyers A.I., and Mihelich E.D. Angew. Chem., Int. Ed. Engl. 15 (1976) 270-281
6. Mayryanoff B.E. In: Turchi I.J. (Ed). Oxazoles and Oxazolines in Organic Synthesis. Chemistry of Heterocyclic Compounds: Oxazoles Vol. 45 (1986), John Wiley & Sons, New York 964-996
7. Meyers A.I., and Shimano M. Tetrahedron Lett. 34 (1993) 4893-4896
8. Ragnarsson U., Grehn L., Monteiro L.S., and Maia H.L.S. Synlett 15 (2003) 2386-2388
9. Laaziri A., Uziel J., and Jugé S. Tetrahedron: Asymmetry 9 (1998) 437-447
10. 4 prior to being concentrated under reduced pressure. The product was purified by column chromatography.