Intramolecular 4+3 cycloadditions. A theoretical analysis of simple diastereoselectivity in reactions of alkoxyallylic cations and furans - Forschungsportal der Justus-Liebig-Universität Gießen:

Journalartikel

Intramolecular 4+3 cycloadditions. A theoretical analysis of simple diastereoselectivity in reactions of alkoxyallylic cations and furans

Autorenliste: Harmata, M; Schreiner, PR

Jahr der Veröffentlichung: 2001

Seiten: 3663-3665

Zeitschrift: Organic Letters

Bandnummer: 3

Heftnummer: 23

ISSN: 1523-7060

DOI Link: https://doi.org/10.1021/ol016611t

Verlag: American Chemical Society

Abstract:
A computational examination (B3LYP/6-31+G*//HF/6-31+G* + ZPVE) of an intramolecular 4 + 3 cycloaddition reaction suggests a stepwise process and the likelihood of reversibility in at least one of the pathways examined.

Autoren/Herausgeber

- Uni.-Prof. Dr. Peter Richard Schreiner, PhD

Zitierstile

Harvard-Zitierstil: Harmata, M. and Schreiner, P. (2001) Intramolecular 4+3 cycloadditions. A theoretical analysis of simple diastereoselectivity in reactions of alkoxyallylic cations and furans, Organic Letters, 3(23), pp. 3663-3665. https://doi.org/10.1021/ol016611t

APA-Zitierstil: Harmata, M., & Schreiner, P. (2001). Intramolecular 4+3 cycloadditions. A theoretical analysis of simple diastereoselectivity in reactions of alkoxyallylic cations and furans. Organic Letters. 3(23), 3663-3665. https://doi.org/10.1021/ol016611t