115091-77-5Relevant academic research and scientific papers
Green chemistry preparation of thiochromeno[4,3-b]pyran and benzo[h]thiazolo[2,3-b]quinazoline derivatives using HSBM technique over ZnAl2o4 nano-powders
Ghashang, Majid,Janghorban, Sadaf,Roudbaraki, Seyyed Jalal
, p. 421 - 427 (2019/10/28)
Aim and Objective: The aim of this paper is to introduce HSBM as a green and environmentally friendly technique for the synthesis of thiochromeno[4,3-b]pyran and benzo[h]thiazolo[2,3-b]quinazoline derivatives over ZnAl2O4 nanopowders
Green chemistry preparation of MgO nanopowders: efficient catalyst for the synthesis of thiochromeno[4,3-b]pyran and thiopyrano[4,3-b]pyran derivatives
Ghashang, Majid,Mansoor, Syed Sheik,Mohammad Shafiee, Mohammad Reza,Kargar, Mahboubeh,Najafi Biregan, Mohammad,Azimi, Fateme,Taghrir, Hadi
, p. 377 - 390 (2016/07/23)
A mild and efficient method for the synthesis of thiochro meno[4,3-b]pyran and thiopyrano[4,3-b]pyran derivatives using MgO nanopowders as a catalyst is described. The MgO nanopowders were prepared via a green biosynthesis method using an extract of Rosma
Synthesis of novel tricyclic heterocyclic compounds as potential anticancer agents using chromanone and thiochromanone as synthons
Hammam, Abou El-Fotooh G.,Fahmy,Amr, Abdel-Galil E.,Mohamed, Ashraf M.
, p. 1985 - 1993 (2007/10/03)
The arylmethylene of benzopyrane or benzothiopyrane 3,4 have been synthesized and condensed with hydrazine, guanidine and thiourea to yield pyrazole 5-8, aminopyrimidine 9,10 and thioxopyrimidine derivatives 11,12, respectively. Compounds 3 or 4 on treatment with malononitrile in the presence of ammonium acetate/acetic acid or in the presence of piperidine/ methanol to yield benzopyrano- and benzothiopyranopyridine 13,14 and benzopyrano- and benzothiopyrane 15,16, respectively. The oxirane of compound 3 is prepared and condensed with CS2 to yield the tricyclic system, thioxothienobenzopyrane 21. Ylidenemalononitrile for the ketone 1 and 2 are synthesized and condensed with aromatic aldehyde in presence of ammonium acetate/acetic acid to yield benzopyranopyridine and benzothiopyranopyridine derivatives 24,25, respectively, which are the isomer of compounds 13,14. Ylidenemalononitrile on condensation with phenylisothiocyanate yields benzo-pyrano- and benzothiopyranothioxopyridine 28,29, respectively.
The synthesis and antifungal activity of 2-amino-4-aryl-4H,5H-benzothiopyranopyran-3-carbonitriles and 2-alkoxy-4-aryl-5H-benzothiopyranopyridine-3-carbonitriles
Nakib, T.A.,Bezjak, V.,Rashid, S.,Fullam, B.,Meegan, M.J.
, p. 221 - 230 (2007/10/02)
This paper describes the synthesis of a series of 2-amino-4-aryl-4H,5H-benzothiopyranopyran-3-carbonitriles and 2-alkoxy-4-aryl-5H-benzothiopyranopyridine-3-carbonitriles.All of these products were studied for antifungal activity and many of these compounds displayed good activity against Cryptococcus neoformans, Torulopsis glabrata, and Trichosporon cutaneum.
