124957-67-1Relevant articles and documents
2-Azetidinones: Synthesis and biological evaluation as potential anti-breast cancer agents
Geesala, Ramasatyaveni,Gangasani, Jagadeesh Kumar,Budde, Mahender,Balasubramanian, Sridhar,Vaidya, Jayathirtha Rao,Das, Amitava
, p. 544 - 558 (2016/09/09)
A series of twenty-five 2-azitidinone (β-lactam) derivatives were synthesized and evaluated for anti-cancer properties against breast cancer, MCF-7 and MDA-MB-231. These β-lactam derivatives depicted significant cytotoxicity in cancer cell lines but not i
Iodine-mediated intramolecular electrophilic aromatic cyclization in allylamines: A general route to synthesis of quinolines, pyrazolo[4,3-b] pyridines, and thieno[3,2-b]pyridines
Batchu, Harikrishna,Bhattacharyya, Soumya,Batra, Sanjay
, p. 6330 - 6333 (2013/02/23)
An unprecedented synthesis of aromatic ring annulated pyridines from suitably substituted primary allylamines via intramolecular electrophilic aromatic cyclization mediated by molecular iodine under mild conditions is described.
Alternate, easy and practical synthesis of allylamines from acetyl derivatives of Baylis-Hillman adducts using methanolic ammonia
Pathak, Richa,Singh, Vijay,Nag, Som N.,Kanojiya, Sanjeev,Batra, Sanjay
, p. 813 - 816 (2007/10/03)
A methanolic ammonia-mediated alternate, easy and practical stereoselective synthesis of allylamines from the acetyl derivatives of Baylis-Hillman adducts is described. Georg Thieme Verlag Stuttgart.
