Intriguing double-inversion stereochemistry in the denitrogenation of 2,3-diazabicyclo[2.2.1]heptene-type azoalkanes: a model mechanistic study in physical organic chemistry
Author:
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Cited by 19 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. A Theoretical Stereoselectivity Model of Photochemical Denitrogenations of Diazoalkanes Toward Strained 1,3-Dihalogenated Bicyclobutanes;The Journal of Organic Chemistry;2021-02-05
2. Heavy-Atom Tunneling Processes during Denitrogenation of 2,3-Diazabicyclo[2.2.1]hept-2-ene and Ring Closure of Cyclopentane-1,3-diyl Diradical. Stereoselectivity in Tunneling and Matrix Effect;The Journal of Organic Chemistry;2020-06-12
3. Synthesis of Benzodihydrofurans by Asymmetric C−H Insertion Reactions of Donor/Donor Rhodium Carbenes;Chemistry – A European Journal;2017-08-10
4. Mechanistic study of stereoselectivity in azoalkane denitrogenations;Pure and Applied Chemistry;2017-06-27
5. Impact of Diradical Spin State (Singlet vs Triplet) and Structure (Puckered vs Planar) on the Photodenitrogenation Stereoselectivity of 2,3-Diazabicyclo[2.2.1]heptanes;The Journal of Physical Chemistry B;2016-07-14
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