Conclusions
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1.
The reaction of 2-alkoxyvinyl compounds of boron with alcohols was studied.
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2.
The boron-carbon bond in trans-2-alkoxyvinyl compounds of boron is cleaved considerably more readily by alcohols than the B-alkyl bond, which is explained by the greater polarity of the B-Csp 2 bond in comparison with the B-Csp 3 bond.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 9, pp. 2023–2028, September, 1970.
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Bubnov, Y.N., Korobeinikova, S.A., Isagulyants, G.V. et al. Organoboron compounds. Russ Chem Bull 19, 1902–1906 (1970). https://doi.org/10.1007/BF00849769
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DOI: https://doi.org/10.1007/BF00849769