A New Perspective in the Lewis Acid Catalyzed Ring Opening of Epoxides. Theoretical Study of Some Complexes of Methanol, Acetic Acid, Dimethyl Ether, Diethyl Ether, and Ethylene Oxide with Boron Trifluoride-Reference-Cited by-同舟云学术

A New Perspective in the Lewis Acid Catalyzed Ring Opening of Epoxides. Theoretical Study of Some Complexes of Methanol, Acetic Acid, Dimethyl Ether, Diethyl Ether, and Ethylene Oxide with Boron Trifluoride

Published:2006-09-19 Issue:41 Volume:110 Page:11734-11751
ISSN:1089-5639
Container-title:The Journal of Physical Chemistry A
language:en
Short-container-title:J. Phys. Chem. A

Author:

Saenz Patricia¹,Cachau Raúl E.¹,Seoane Gustavo¹,Kieninger Martina¹,Ventura Oscar N.¹

Affiliation:

1. Computational Chemical Physics Group, Detema, and Department of Organic Chemistry, Faculty of Chemistry, Universidad de la República (Udelar), CC1157, Avda. Gral. Flores 2124, 11800 Montevideo, Uruguay, and Advanced Biomedical Computing Center, National Cancer Institute-Frederick, SAIC-Frederick Inc., Frederick, Maryland 21702-1201

Publisher

American Chemical Society (ACS)

Subject

Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jp061359y

Reference95 articles.

1. Stereoselectivity in the boron trifluoride catalyzed rearrangement of a 1,1-disubstituted ethylene oxide

2. Studies in Stereochemistry. II. Steric Strains as a Factor in the Relative Stability of Some Etherates of Boron Fluoride

3. Donor-Acceptor Bonding. I. Etherates of Boron Trifluoride1

4. Donor-Acceptor Bonding. II. An Electron Diffraction Investigation of the Structure of Dimethyl Ether-Boron Trifluoride

5. On the Structure of Dimethyl Ether-Boron Trifluoride

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