Aminals in the Synthesis of 1,3-Substituted Propargylamines and 3H-2-Vinylidene-3-Aminobenzofuran Derivatives
Document Type
Article
Language
eng
Publication Date
3-1994
Publisher
Springer
Source Publication
Russian Chemical Bulletin
Source ISSN
1066-5285
Abstract
Aminals of aromatico-hydroxyaldehydes react when heated with terminal acetylenes to form, depending on the reaction conditions and the nature of the starting compounds, 1,3-substituted propargylamines or 3H-2-vinylidene-3-aminobenzofuran derivatives, the structures of which were established by X-ray diffraction.
Recommended Citation
Ukhin, L. Yu; Komissarov, V. N.; Lindeman, Sergey; Khrustalev, V, N,; and Struchkov, Yu T., "Aminals in the Synthesis of 1,3-Substituted Propargylamines and 3H-2-Vinylidene-3-Aminobenzofuran Derivatives" (1994). Chemistry Faculty Research and Publications. 684.
https://epublications.marquette.edu/chem_fac/684
Comments
Russian Chemical Bulletin, Vol. 43, No. 3 (March 1994): 413-419. DOI.
Sergey Lindeman was affiliated with Russian Academy of Sciences at the time of publication.