α-Aminoester-Derived Imidazoles by 1,5-Electrocyclization of Azavinyl Azomethine Ylides-Reference-Cited by-同舟云学术

α-Aminoester-Derived Imidazoles by 1,5-Electrocyclization of Azavinyl Azomethine Ylides

Published:2009-06-10 Issue:13 Volume:11 Page:2840-2843
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Attanasi Orazio A.¹,Caselli Emilia¹,Davoli Paolo¹,Favi Gianfranco¹,Mantellini Fabio¹,Ori Claudia¹,Prati Fabio¹

Affiliation:

1. Istituto di Chimica Organica, Università degli Studi di Urbino “Carlo Bo”, via I Maggetti 24, 61029 Urbino, Italy, and Dipartimento di Chimica, Università degli Studi di Modena e Reggio Emilia, via Campi 183, 41100 Modena, Italy

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol901051z

Reference53 articles.

1. For reviews on azomethine ylides, see:aHuisgen, R.1,3-Dipolar Cycloaddition Chemistry;Padwa, A., Ed.Wiley:New York, 1984; Vol. 1, pp1−177.

2. bTufariello, J. J.1,3-Dipolar Cycloaddition Chemistry;Padwa, A., Ed.Wiley:Chichester, UK, 1984; Vol. 2, pp83−168.

3. Asymmetric 1,3-Dipolar Cycloaddition Reactions

4. dHarwood, L. M.; Vickers, R. J.The Chemistry of Heterocyclic Compounds: Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry toward Heterocycles and Natural Products;Padwa, A.; Pearson, W. H., Eds.Wiley and Sons:New York, 2002; Vol. 59, pp169−252.

5. Azomethine Ylides in Organic Synthesis

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