Abstract
This study investigated the regioselectivity of the intramolecular biaryl coupling reaction of the phenyl benzoate derivative which possesses a methyl or methoxy group at the meta-position of the phenoxy moiety. The type of base and the presence/absence of the phosphine ligand influenced the product ratio. A transition state model and the regioselectivity of the reaction are discussed.
Original language | English |
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Pages (from-to) | 621-628 |
Number of pages | 8 |
Journal | Heterocycles |
Volume | 88 |
Issue number | 1 |
DOIs | |
Publication status | Published - 2014 |
ASJC Scopus subject areas
- Analytical Chemistry
- Pharmacology
- Organic Chemistry