Yusubov, Mekhman, Soldatova, Natalia, Postnikov, Pavel, Valiev, Rashid, Svitich, Dmitry, Yusubova, Roza, Yoshimura, Akira, Wirth, Thomas ![]() |
Preview |
PDF
- Accepted Post-Print Version
Download (627kB) | Preview |
Abstract
New substituted 1-arylbenziodoxolones were prepared and their reactivity with azide anion nucleophile was investigated. It was found that independent on the presence of substituents, all reactions of 1-arylbenziodoxolones proceed as nucleophilic substitution of the iodonium leaving group in the electron-deficient benziodoxolone benzene ring. The presence of bulky substituents in the ortho-position of the aryl ring slowers the reaction, while the presence of a moderately electron-withdrawing bromine substituent in the para-position to iodine in the benziodoxolone ring moderately increases the rate of substitution. The presence of a strongly electron-withdrawing nitro group in the para-position to iodine in the benziodoxolone ring dramatically increases the rate of substitution. These observations are in agreement with the electronic requirements for internal nucleophilic substitution in the benziodoxole ring. A quantum-chemical computational study of the possible reaction paths is in agreement with the observed effects of substituents on the reactivity of arylbenziodoxolones in this reaction.
Item Type: | Article |
---|---|
Date Type: | Publication |
Status: | Published |
Schools: | Chemistry |
Publisher: | Wiley |
ISSN: | 1434-193X |
Date of First Compliant Deposit: | 10 January 2018 |
Date of Acceptance: | 3 January 2018 |
Last Modified: | 07 Nov 2023 00:35 |
URI: | https://orca.cardiff.ac.uk/id/eprint/108045 |
Citation Data
Cited 9 times in Scopus. View in Scopus. Powered By Scopus® Data
Actions (repository staff only)
![]() |
Edit Item |