Reply to “Comment on ‘The Mechanism of Pyrolysis of Benzyl Azide: Spectroscopic Evidence for Benzemethanimine Formation’”
Author:
Affiliation:
1. LIBPhys−Laboratório de Instrumentação, Engenharia Biomédica e Física da Radiação Departamento de Física, Faculdade de Ciências e Tecnologia, FCT, 2829-516 Caparica, Portugal
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.jpca.5b04334
Reference10 articles.
1. Comment on “The Mechanism of Pyrolysis of Benzyl Azide: Spectroscopic Evidence for Benzenemethanimine Formation”
2. The Mechanism of Pyrolysis of Benzyl Azide: Spectroscopic Evidence for Benzenemethanimine Formation
3. New Reactions ofN-tert-Butylimines; Formation of N-Heterocycles by Methyl Radical Elimination on Flash Vacuum Thermolysis ofN-Benzylidene- andN-(2-Pyridylmethylidene)-tert-butylamines
4. Reinvestigation of the formaldehyde–aniline condensation. Part 4. Ultraviolet photoelectron and electron transmission spectra of N-methyleneaniline and its symmetric dimethyl ring-substituted homologues and semiempirical theoretical evaluations
5. Intramolecular Hydrogen Transfer in (2-Aminophenyl)carbene and 2-Tolylnitrene. Matrix Isolation of 6-Methylene-2,4-cyclohexadien-1-imine
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1. Continuous Flow-Facilitated CB2 Agonist Synthesis, Part 1: Azidation and [3 + 2] Cycloaddition;Organic Process Research & Development;2023-03-30
2. Synthesis and use of a hyper-connecting cross-linking agent in the hole-transporting layer of perovskite solar cells;Journal of Materials Chemistry A;2017
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