Intramolecular 4+3 cycloadditions. A theoretical analysis of simple diastereoselectivity in reactions of alkoxyallylic cations and furans - Research portal of Justus Liebig University Giessen:

Journal article

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

Authors list: Harmata, M; Schreiner, PR

Publication year: 2001

Pages: 3663-3665

Journal: Organic Letters

Volume number: 3

Issue number: 23

ISSN: 1523-7060

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

Publisher: 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.

Authors/Editors

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

Citation Styles

Harvard Citation style: 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 Citation style: 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