Stereoselectivity of the aza-Diels–Alder reaction between cyclopentadiene and protonated phenylethylimine derived from glyoxylates. A density functional theory study

Filipe Teixeira; José E. Rodríguez-Borges; André Melo; M. Natália D.S. Cordeiro

doi:10.1016/j.cplett.2009.06.009

journal article Jul 01, 2009

Stereoselectivity of the aza-Diels–Alder reaction between cyclopentadiene and protonated phenylethylimine derived from glyoxylates. A density functional theory study

Filipe Teixeira

José E. Rodríguez-Borges

André Melo M. Natália D.S. Cordeiro

Chemical Physics Letters Vol. 477 No. 1-3 pp. 60-64 · Elsevier BV

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References

Details

Published: Jul 01, 2009
Vol/Issue: 477(1-3)
Pages: 60-64
License: View

Authors

F

Filipe Teixeira

LAQV-REQUIMTE, Faculty of Sciences of the University of Porto, Rua do Campo Alegre, 4169-007 Porto, Portugal

J

José E. Rodríguez-Borges

Department of Chemistry and Biochemistry, Faculty of Sciences, LAQV/REQUIMTE, University of Porto, Porto 4169-007, Portugal

A

André Melo

M

M. Natália D.S. Cordeiro

Cite This Article

Filipe Teixeira, José E. Rodríguez-Borges, André Melo, et al. (2009). Stereoselectivity of the aza-Diels–Alder reaction between cyclopentadiene and protonated phenylethylimine derived from glyoxylates. A density functional theory study. Chemical Physics Letters, 477(1-3), 60-64. https://doi.org/10.1016/j.cplett.2009.06.009

Stereoselectivity of the aza-Diels–Alder reaction between cyclopentadiene and protonated phenylethylimine derived from glyoxylates. A density functional theory study

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