Diverse chemical behaviour of 2-hydroxy-functionalized pyrroline-1-oxide

Tetrahedron Letters

Volumn 51, Issue 44, 2010, Pages 5801-5803

  Buchlovič, Marian ^a   Man, Stanislav ^a   Potáček, Milan ^a  

^a MASARYK UNIVERSITY   (Czech Republic)

Author keywords

[No Author keywords available]

Indexed keywords

2 HYDROXY 3,3,5 TRIMETHYL 3,4 DIHYDRO 2H PYRROLE 1 OXIDE; NITRONE; OXIDE; PYRROLE DERIVATIVE; PYRROLINE 1 OXIDE; REAGENT; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; REACTION ANALYSIS; REACTION TIME; X RAY ANALYSIS;

EID: 77957571288     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.08.103     Document Type: Article

References (8)

1. Padwa, A.; Pearson, W. H. Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products, John Wiley & Sons: New York, 2002.
2. M. Buchlovi, S. Man, and M. Potáek Tetrahedron 64 2008 9953
3. M. Buchlovi, S. Man, K. Kislitsõn, Ch. Mathot, and M. Potáek Tetrahedron 66 2010 1821
4. S. Man, M. Buchlovi, and M. Potáek Tetrahedron Lett. 47 2006 6961
5. J.B. Bapat, and A. Durie Aust. J. Chem. 37 1984 211
6. Crystallographic data for compounds 2b (CCDC deposition number 767570) and 5a (CCDC deposition number 767571) have been deposited at the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK.
7. Carbon (grey), oxygen (red), nitrogen (blue) and sulfur (yellow) atoms are drawn as principal ellipses (70% probability level); hydrogen atoms are drawn as fixed-size spheres (cyan).
8. Based on an NMR study of crude reaction mixtures.