NMR and DFT studies on persistent carbocations derived from benzo[kl ]xanthene, dibenzo[d ,d ′]benzo[1,2-b :4,3-b ′]difuran, and dibenzo[d ,d ′]benzo[1,2-b :4,5-b ′]difuran in superacidic media-Reference-Cited by-同舟云学术

NMR and DFT studies on persistent carbocations derived from benzo[kl ]xanthene, dibenzo[d ,d ′]benzo[1,2-b :4,3-b ′]difuran, and dibenzo[d ,d ′]benzo[1,2-b :4,5-b ′]difuran in superacidic media

Published:2015-09-28 Issue:2 Volume:29 Page:107-111
ISSN:0894-3230
Container-title:Journal of Physical Organic Chemistry
language:en
Short-container-title:J. Phys. Org. Chem.

Author:

Okazaki Takao¹,Nakagawa Madoka¹,Futemma Takeshi¹,Kitagawa Toshikazu¹

Affiliation:

1. Department of Chemistry for Materials, Graduate School of Engineering; Mie University; Tsu Mie 514-8507 Japan

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/poc.3505/fullpdf

Reference50 articles.

1. Superacid Chemistry

2. Recent Developments in Carbocation and Onium Ion Chemistry

3. Scales of Lewis Basicities toward C-Centered Lewis Acids (Carbocations)

4. Photogeneration of carbocations: applications in physical organic chemistry and the design of suitable precursors

5. A Practical Guide for Estimating Rates of Heterolysis Reactions

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