Synthesis of Schiff bases and oxazolidines from 2-amino-4-phenylthiazole
摘要:
Reactions of 2-amino-4-phenylthiazole with aromatic aldehydes gave the corresponding Schiff bases which were reduced with sodium tetrahydridoborate to amines. Reactions of the Schiff bases with 2-methyloxirane, 2-chloromethyloxirane, and 2-phenoxymethyloxirane led to the formation of 2,5-disubstituted 3-(4-phenylthiazol-2-yl)oxazolidines.
SONDHI S. M.; BHATTI A. M.; MAHAJAN M. P.; RALHAN N. K., J. INDIAN CHEM. SOC. <JICS-AH>, 1975, 52, NO 1, 49-50
作者:SONDHI S. M.、 BHATTI A. M.、 MAHAJAN M. P.、 RALHAN N. K.
DOI:——
日期:——
Synthesis of Schiff bases and oxazolidines from 2-amino-4-phenylthiazole
作者:S. E. Sadigova、A. M. Magerramov、M. A. Allakhverdiev
DOI:10.1134/s107042800812018x
日期:2008.12
Reactions of 2-amino-4-phenylthiazole with aromatic aldehydes gave the corresponding Schiff bases which were reduced with sodium tetrahydridoborate to amines. Reactions of the Schiff bases with 2-methyloxirane, 2-chloromethyloxirane, and 2-phenoxymethyloxirane led to the formation of 2,5-disubstituted 3-(4-phenylthiazol-2-yl)oxazolidines.
Sondhi,S.M. et al., Journal of the Indian Chemical Society, 1975, vol. 52, p. 49 - 50