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Квантовохимическое обоснование природы интермедиата и региоселективности гомолитического окислительного сочетания L-цистеина

Квантовохимическое обоснование природы интермедиата и региоселективности гомолитического окислительного сочетания L-цистеина

Abstract

A quantum chemical substantiation of the intermediate (thiyl radical) nature and reaction regioselectivity (S,S-coupling) of the L-cysteine homolytic oxidative dimerization resulting by the L-cystine formation has been carried out. The electrostatic factor does not prevent the reaction occurrence.

Предпринято квантовохимическое обоснование природы интермедиата (тиильный радикал) и региоселективности (S,S-сочетание) реакции гомолитической окислительной димеризации L-цистеина с образованием L-цистина. Протеканию реакции не препятствует электростатический фактор.

Keywords

ЦИСТЕИН, ГОМОЛИТИЧЕСКОЕ ОКИСЛИТЕЛЬНОЕ СОЧЕТАНИЕ, ИНТЕРМЕДИАТ, РЕГИОСЕЛЕКТИВНОСТЬ, СПИНОВАЯ ПЛОТНОСТЬ, ЭЛЕКТРОСТАТИЧЕСКИЙ ФАКТОР, КВАНТОВОХИМИЧЕСКОЕ ИССЛЕДОВАНИЕ

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
0
Average
Average
Average