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Theoretical Investigation on Regioselectivities of Diels-Alder Reactions by Conjugated Effect

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摘要 of main observation and conclusion The regioselectivities of 76 Diels-Alder reactions between unsymmetrical dienes and dienophiles were investigated by local softness and generalized local softness at atomic and chemical bond view,respectively,where the reactivity descriptors were calculated by finite difference approximation and ABEEMan model.Based on local HSAB principle and matching criterion of local softness,reasonable explanation and prediction on regioselectivities of all reactions through ABEEMan model have been obtained,which are in agreement with the experimental results.Especially,at n-bond level,while the 1-substituents of dienes were NH2/NMe2,and NEt2/because of the p-R conjugated effect between the lone pairs of Natom and the conjugated n-bond of the four double-bonded carbon atoms in diene,it made the dienophile not easy to approach diene by Manner A,hence,Manner B can forecast the ortho regioisomer as main product well,and Manner A cannot.As to the other reactions,both Manner A and Manner B can predict their regioselectivities.It can be seen that the ABEEMan model can take the effect of the chemical environment on the reaction reactivity into account richly,especially the system includes n-bond and lone pairs.However,the results through the finite difference approximation are not reasonable.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2020年第12期1696-1702,共7页 中国化学(英文版)
基金 This work was supported by the National Natural ScienceFoundation of China(No.21473083) Liaoning Normal University,the Research foundation for Advanced Talents of cast China University of Technology(No.DHBK2019139) the open Founda-tion of Jiangxi Province kev Laboratory of the Causes and Controlof Atmospheric Pollution from East China University of Technology(No.AE1904).
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