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This article is cited in 9 scientific papers (total in 9 papers)
Configurations of 1,3-bis(aryl)-1,3-diaza-2-thiaallenes in the crystal state
I. Yu. Bagryanskaya, Yu. V. Gatilov, A. V. Zibarev
N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation
Abstract:
The σ,π-mixing responsible for the Z,Z configuration of the title compounds is indifferent to both withdrawing (NO2) and releasing (OMe) π-electron character of ortho-substituents, and the arrangement of aromatic rings in the Z,E configuration orthogonally to the NSN plane is a universal way to overcome steric hindrances due to bulky (But, Br) ortho-substituents.
Citation:
I. Yu. Bagryanskaya, Yu. V. Gatilov, A. V. Zibarev, “Configurations of 1,3-bis(aryl)-1,3-diaza-2-thiaallenes in the crystal state”, Mendeleev Commun., 9:4 (1999), 157–158
Linking options:
https://www.mathnet.ru/eng/mendc4572 https://www.mathnet.ru/eng/mendc/v9/i4/p157
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