22272-29-3Relevant articles and documents
Synthesis of eight-, nine-, and ten-membered, nitrogen-containing quinone-fused heterocycles
Yerushalmi, Sarit,Lemcoff, N. Gabriel,Bittner, Shmuel
, p. 239 - 242 (2007)
A series of allylamino-, diallylamino-, homoallylamino-and bishomoallylamino naphthoquinones were synthesized. Ruthenium-mediated ring-closing metathesis (RCM) efficiently converted these substrates into novel eight-, nine-, and ten-membered quinone-fused heterocycles. Hydro-derivatives of diazacine, diazonine, and diazecine were isolated and characterized. Georg Thieme Verlag Stuttgart.
'On water' assisted synthesis and biological evaluation of nitrogen and sulfur containing hetero-1,4-naphthoquinones as potent antifungal and antibacterial agents
Tandon, Vishnu K.,Maurya, Hardesh K.,Verma, Manoj K.,Kumar, Rohitashw,Shukla, Praveen K.
scheme or table, p. 2418 - 2426 (2010/07/05)
2-Chloro-3-(4-methylpiperazin-1-yl)naphthalene-1,4-dione (3a), 2-chloro-3-(pyrrolidin-1-yl)naphthalene-1,4-dione (3b), 2-chloro-3-(piperidin-1-yl)naphthalene-1,4-dione (3c), 2-chloro-3-morpholinonaphthalene-1,4-dione (3d), 2-chloro-3-(2-phenylhydrazinyl)n
Relation between the chemical structure and the antitubercular effect of alpha-naphthoquinone derivatives substituted in 2 and 3 positions.
OERIU
, p. 266 - 272 (2007/10/10)
-