145089-91-4Relevant academic research and scientific papers
Crystal and molecular structure of 1-phenyl-3-(2-hydroxyphenylamino)-2-buten-1-one, C16H15NO2
Glowiak, Tadeusz,Sobczak, Jaroslaw M.
, p. 673 - 678 (1992)
Orange, yellow, and colorless crystals were obtained for the title compound.The orange crystals are triclinic, space group P, a=9.181(2), b=10.734(2), c=15.245(3) Angstroem, α=73.06(2), β=79.21(2), χ=67.83(2) deg, V=1325.9(5) Angstroem3, Z=4
Structural and spectral studies of 3-(2-hydroxyphenylimino)-1-phenylbutan-1-one and its diorganotin(IV) complexes
Dey, Dilip Kumar,Dey, Sankar Prasad,Karan, Nirmal Kumar,Datta, Amitabha,Lycka, Antonin,Rosair, Georgina M.
, p. 2434 - 2441 (2009)
Two diorganotin(IV) complexes of the general formula R2Sn[Ph(O)C{double bond, long}CH-C(Me){double bond, long}N-C6H4(O)] (R = Ph, 1a; R = Me, 1b) have been synthesized from the corresponding diorganotin(IV) dichlorides and
Acid-promoted cleavage of the C–C double bond of N-(2-Hydroxylphenyl)enaminones for the synthesis of benzoxazoles
Ge, Bailu,Peng, Yanling,Liu, Jing,Wen, Si,Peng, Cheng,Cheng, Guolin
, (2019/12/09)
An acid-mediated selective cleavage of C–C double bond of N-(2-hydroxylphenyl)enaminones with formation a new C–O bond for the synthesis of 2-substituted benzoxazoles has been developed. This protocol proceeds under transition metal- and oxidant-free conditions with broad functional group tolerance. The oxidative cleavage of C–C double bond of N-(2-hydroxylphenyl)enaminone is also realized using NCS or NFSI as oxidants with release of 2,2-dihalogen-acetophenone fragments.
