Hyperconjugation enhances electrophilic addition to monocyclic monoterpenes: a Fukui function perspective-Reference-Cited by-同舟云学术

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Hyperconjugation enhances electrophilic addition to monocyclic monoterpenes: a Fukui function perspective

Published:2018-09-29 Issue:10 Volume:24 Page:
ISSN:1610-2940
Container-title:Journal of Molecular Modeling
language:en
Short-container-title:J Mol Model

Author:

Amador-Balderas Jorge A.,Ramírez Ramsés E.,Méndez Francisco,Meléndez Francisco J.,Richaud Arlette

Publisher

Springer Science and Business Media LLC

Subject

Computational Theory and Mathematics,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Catalysis

Link

http://link.springer.com/article/10.1007/s00894-018-3825-2/fulltext.html

Reference31 articles.

1. Slade JH, de Perre C, Lee L, Shepson PB (2017) Nitrate radical oxidation of γ-terpinene: hydroxy nitrate, total organic nitrate, and secondary organic aerosol yields. Atmos Chem Phys 17:8635–8650. https://doi.org/10.5194/acp-17-8635-2017

2. Harrison JC, Wells JR (1994) Investigation of terpinolene + ozone or terpinolene + nitrate radical reaction products using denuder/filter apparatus. Atmos Environ 80:524–532

3. Keywood MD, Varutbangkul V, Bahreini R, Flagan RC, Seinfeld JH (2004) Secondary organic aerosol formation from the ozonolysis of cycloalkenes and related compounds. Environ Sci Technol 38:4157–4164

4. Jiang L, Wang W, Xu Y-S (2009) Theoretical investigation of the NO3 radical addition to double bonds of limonene. Int J Mol Sci 10:3743–3754

5. Jiang L, Lan R, Xu Y-S, Zhang W-J, Yang W (2013) Reaction of stabilized Criegee intermediates from ozonolysis of limonene with water: ab initio and DFT study. Int J Mol Sci 14:5784–5805

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