64227-37-8Relevant academic research and scientific papers
Hydrazonoyl halides as precursors for new fused heterocycles of 5α-reductase inhibitors
Farghaly, Thoraya A.,Gomha, Sobhi M.,Abbas, Eman M. H.,Abdalla, Mohamed M.
, p. 117 - 122 (2012)
A new series of benzo[6,7]cyclohepta[1,2-d]triazolo[4,3-a]pyrimidines 8a-l was synthesized via reaction of heterocyclic thione 4 or its methyl derivatives 10 with hydrazonoyl halides 5a-l. Also, reaction of compound 4 with a mixture of chloroacetic acid a
(E)-2-Benzylidenebenzocyclanones: Part XIII - (E)/(Z)-Isomerization of some cyclic chalcone analogues. Effect of ring size on lipophilicity of geometric isomers
Perjsi, Pl
, p. 1275 - 1281 (2015/12/31)
Optimized isocratic reverse phase high-performance liquid chromatography (RP-HPLC) method was developed for separation of the respective (E) and (Z) isomers of the cyclic chalcone analogues (E)-2-(4′-X-benzylidene)-1-indanones, -tetralones, and -benzosube
Synthesis of 3,3a-trans/cis-2-phenyl/acetyl-3-aryl-tetrahydroindeno/naphtho-and hexahydrobenzocycloheptapyrazoles as antiimplantation agents
Sinha, Anoop Kumar,Rastogi, Shri Nivas
, p. 684 - 692 (2007/10/02)
Reaction of benzocycloalkanones (1-3 and 24) and araldehydes (4-6) gives the arylideno-alkanones (7-12, 25 and 26) of which 11 and 12 on alkylation and acetylation afford alkyl ethers (13, 14 and 17) and acetates (15 and 16) respectively.Condensation of a
Heterocycles. Part X. Synthesis of New Pyrimidine Systems
El-Rayyes, N. R.,Ramadan, H. M.
, p. 589 - 596 (2007/10/02)
Selected aryl aldehydes I were reacted with 1-benzosuberone to give the corresponding 2-arylidene-1-benzosuberone II.Condensation of these chalcones with urea and thiourea revealed the formation of the corresponding substituted pyrimidin-2-ones III, and p
