Investigating the site-, regio-, and stereo-selectivities of the reactions between organic azide and 7-heteronorbornadiene: a DFT mechanistic study.

Abstract

The site-, regio-, and stereo-selectivities of the title reactions have been studied using density functional theory (DFT) at the M06/6-311G(d,p) level of theory. The effects of substituents on both the three-atom component (TAC) and norbornadiene derivatives have been investigated with a focus on the site-selectivity. The reaction of benzylazide with (1S,4R)-2-tosyl-7-oxabicyclo[2.2.1]hepta-2,5-diene and (1R,4S)-2-bromo-3-tosyl-7-oxabicyclo[2.2.1]hepta-2,5-diene proceeds via addition across the substituted olefinic bond of the two norbornadiene derivatives. Substituents on the TAC do not affect the selectivity of the reaction while substituents on the norbornadiene significantly affect the selectivity of the reaction. Benzylazide preferentially adds across the substituted olefinic bond of the norbornadiene derivative when strong electron-withdrawing group (EWGs) and electron-releasing group (ERGs) substituents are on the norbornadiene while weak ERGs and EWGs on the norbornadiene significantly decreases the site-selectivity such that addition across either double is no longer favored over the other. The formation of exo-cycloadducts is generally favored over the endo-cycloadducts. The reaction of benzylazide and norbornadiene derivatives is a highly irreversible exergonic reaction. The direction of electron density flux is dependent on the nature of the substituent on the reactants. Global reactivity indices and Parr function calculations are in good agreement with the activation barriers and the selectivity of the reactions.