Peri-, Chemo-, Regio-, Stereo- and Enantio-Selectivities of 1,3-dipolar cycloaddition reaction of C,N-Disubstituted nitrones with disubstituted 4-methylene-1,3-oxazol-5(4H)- one: A quantum mechanical study

The peri-, chemo-, regio-, stereo- and enantio-selectivities of 1,3-dipolar cycloaddition reaction of C,N-disubstituted nitrones with disubstituted 4-methylene-1,3-oxazol-5(4H)-one have been studied using density functional theory (DFT) at the M06–2X/6-311G (d,p) level of theory. The 1,3-dipole pref...

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Veröffentlicht in:	Journal of molecular graphics & modelling 2020-06, Vol.97, p.107542-107542, Article 107542
Hauptverfasser:	Pipim, George Baffour, Opoku, Ernest, Tia, Richard, Adei, Evans
Format:	Artikel
Sprache:	eng
Schlagworte:	1,3-Dipole 4-Methylene-1,3-oxazol-5(4H)-One Density functional theory Dipolarophile Spirocycloadduct
Online-Zugang:	Volltext
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