786669-29-2Relevant academic research and scientific papers
Design, synthesis and evaluation of 3-arylidene azetidin-2-ones as potential antifungal agents against Alternaria solani Sorauer
Delong, Wang,Yongling, Wu,Lanying, Wang,Juntao, Feng,Xing, Zhang
, p. 6661 - 6673 (2017/11/17)
A new concise and facile method was explored to synthesize a collection of new 3-arylidene azetidin-2-ones, which could be regarded as the derivatives of the hybrid scaffold of bioactive natural cinnamamide and heterocycle azetidi-2-one. The structures of
Oxidative heck coupling of allylic amines with 2,2,6,6- Tetramethylpiperidine-N-oxyl (TEMPO) as oxidant for the preparation of tetrasubstituted alkenes
He, Zhiheng,Wibbeling, Birgit,Studer, Armido
, p. 3639 - 3647 (2014/01/06)
The paper describes the oxidative Heck arylation of various allylic amines using arylboronic acids for the preparation of tetrasubstituted alkenes. As oxidant the commercially available 2,2,6,6-tetramethylpiperidine-N-oxyl (TEMPO) is used and coupling rea
Cerium(IV) ammonium nitrate catalyzed synthesis of α-dehydro-β-amino esters
Paira, Moumita,Mandal, Samir Kumar,Roy, Subhas Chandra
, p. 2432 - 2434 (2008/09/20)
α-Dehydro-β-amino esters have been synthesized regioselectively from acetates of Baylis-Hillman adducts with amines in the presence of a catalytic amount of ceric ammonium nitrate (CAN) in good yield. The regioselectivity does not differ with respect to t
Synthesis of 4b,5,10a,11-tetrahydroindeno[1,2-b]quinolin-10-ones from Baylis-Hillman adducts
Lee, Chang Gon,Lee, Ka Young,Gowrisankar, Saravanan,Kim, Jae Nyoung
, p. 7409 - 7413 (2007/10/03)
We developed an efficient synthetic method for indenoquinoline skeletons from Baylis-Hillman adducts. 4b,5,10a,11-Tetrahydroindeno[1,2-b]quinolin-10-ones and 7H-indeno[2,1-c]quinolines were prepared from Baylis-Hillman adducts in polyphosphoric acid.
