Charge redistribution in the SpnF-catalyzed Diels–Alder reaction

Charge redistribution in the SpnF-catalyzed Diels–Alder reaction Full article

Journal

Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436

Output data

Year: 2017, Volume: 27, Number: 5, Pages: 500-502 Pages count : 3 DOI: 10.1016/j.mencom.2017.09.024

Authors

Medvedev Michael G. ^1,2 , Novikov Fedor N. ² , Bushmarinov Ivan S. ¹ , Zeifman Alexey A. ² , Polkovnichenko Michael S. ³ , Stroganov Oleg V. ² , Chilov Ghermes G. ² , Lyssenko Konstantin A. ¹ , Svitanko Igor V. ²

Affiliations

1	A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 119991 Moscow, Russian Federation
2	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russian Federation
3	Moscow State High School No. 192, 119334 Moscow, Russian Federation

Investigation of charge delocalization (redistribution) in a SpnF-catalyzed reaction that proceeds through overlapping Diels–Alder and bis-pericyclic mechanisms has shown that it is better represented as a nonpolar cycloaddition rather than a cationic rearrangement.

Medvedev M.G. , Novikov F.N. , Bushmarinov I.S. , Zeifman A.A. , Polkovnichenko M.S. , Stroganov O.V. , Chilov G.G. , Lyssenko K.A. , Svitanko I.V.
Charge redistribution in the SpnF-catalyzed Diels–Alder reaction
Mendeleev Communications. 2017. V.27. N5. P.500-502. DOI: 10.1016/j.mencom.2017.09.024 WOS Scopus OpenAlex

Web of science:	WOS:000413618800024
Scopus:	2-s2.0-85030122015
OpenAlex:	W2758296653

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