25299-18-7Relevant academic research and scientific papers
The Quest of Excited-State Intramolecular Proton Transfer via Eight-Membered Ring π-Conjugated Hydrogen Bonding System
Meng, Fan-Yi,Hsu, Yen-Hao,Zhang, Zhiyun,Wu, Pei-Jhen,Chen, Yi-Ting,Chen, Yi-An,Chen, Chi-Lin,Chao, Chi-Min,Liu, Kuan-Miao,Chou, Pi-Tai
, p. 3010 - 3015 (2017)
Searching for eight-membered ring π-conjugated hydrogen bonding (8-MR H-bonding) systems with excited-state intramolecular proton transfer (ESIPT) property is seminal and synthetically challenging. In this work, a series of π-conjugated molecules (8-HB-1,
DMAP-Catalyzed Reaction of Diethyl 1,3-Acetonedicarboxylate with 2-Hydroxybenzylideneindenediones: Facile Synthesis of Fluorenone-Fused Coumarins
Shkoor, Mohanad,Bayari, Raghad
, p. 795 - 799 (2021/03/01)
The base-catalyzed reaction of diethyl 1,3-acetonedicarboxylate with 2-hydroxybenzylidene indenediones was studied. The reaction provides a facile and expeditious protocol for the synthesis of natural product inspired fluorenone-fused coumarins in good to
Synthesis and characterization of 2-benzylidene-1,3-indandione derivatives as in vitro quantification of amyloid fibrils
Adibi, Hadi,Mehrabi, Maryam,Amiri, Kazhal,Balalaie, Saeed,Khodarahmi, Reza
, p. 423 - 432 (2019/11/03)
Timely detection of amyloid aggregations has a critical role in the treatment of degenerative nervous system disorders such as Alzheimer’s, Parkinson’s disease and systemic amyloidosis. Thioflavin T (ThT) is a dye considered for the detection of amyloids.
Diversity-oriented synthesis of chromenopyrrolidines from azomethine ylides and 2-hydroxybenzylidene indandiones via base-controlled regiodivergent (3+2) cycloaddition
Yu, Jhen-Kuei,Chien, Han-Wei,Lin, Yi-Jung,Karanam, Praneeth,Chen, Yu-Heng,Lin, Wenwei
supporting information, p. 9921 - 9924 (2018/09/11)
An organobase-directed, regiodivergent 1,3-dipolar cycloaddition of azomethine ylides and 2-hydoxybenzylidene indandiones is reported. The scarcely explored reversal of the nucleophilic site in azomethine ylides has been exploited for their regiodivergent (3+2) cycloaddition, which subsequently resulted in two different cascade processes to generate functionally distinct chromenopyrrolidines in a diversity oriented manner.
Chemo- and Diastereoselective Michael-Michael-Acetalization Cascade for the Synthesis of 1,3-Indandione-Fused Spiro[4.5]decan Scaffolds
Yang, Shu-Mei,Tsai, Yi-Ling,Reddy, Ganapuram Madhusudhan,M?hlmann, Lennart,Lin, Wenwei
, p. 9182 - 9190 (2017/09/11)
A novel, organobase-catalyzed and highly chemoselective Michael-Michael-acetalization cascade is presented for the efficient synthesis of spiro-indandione skeletons. Following this very simple protocol, a broad range of products was obtained in good yield
A Chemical Disruptor of the ClpX Chaperone Complex Attenuates the Virulence of Multidrug-Resistant Staphylococcus aureus
Fetzer, Christian,Korotkov, Vadim S.,Th?nert, Robert,Lee, Kyu Myung,Neuenschwander, Martin,von Kries, Jens Peter,Medina, Eva,Sieber, Stephan A.
supporting information, p. 15746 - 15750 (2017/10/20)
The Staphylococcus aureus ClpXP protease is an important regulator of cell homeostasis and virulence. We utilized a high-throughput screen against the ClpXP complex and identified a specific inhibitor of the ClpX chaperone that disrupts its oligomeric sta
Aqueous extract of Balanites roxburghii fruit: A green dispersant for C-C bond formation
Barge, Madhuri,Salunkhe, Rajashri
, p. 31177 - 31183 (2014/08/05)
An aqueous biosurfactant solution, a biobased green acidic catalyst for Knoevenagel condensation of 1,3-indanedione with aryl aldehydes and tandem Knoevenagel-Michael reaction of 3-methyl-1-phenylpyrazole with aryl aldehydes, has been reported for the fir
Clean synthesis of 2-arylideneindan-1,3-diones in water
Yang, Peng Hui,Zhang, Qun Zheng,Sun, Wei
experimental part, p. 1063 - 1068 (2012/08/28)
A high-yield synthesis of 2-arylideneindan-1,3-diones in water was achieved by the Knoevenagel condensation of indan-1,3-dione with aromatic aldehydes at ambient temperature avoiding the addition of any catalyst. The procedure is simple, efficient, as wel
Synthesis and antimicrobial study of novel 1-aryl-2-oxo-indano[3,2-d] pyrido/pyrimido[1,2-b]pyrimidines
Sarvesh, Pandey K.,Nizamuddin, Khan
experimental part, p. 418 - 423 (2009/04/04)
A series of 2-(arylidene)-indan-1, 3-diones 1 were prepared by Knoevenagel reaction between indane-1,3-dione and the appropriate araldehydes. The α,β-enones 1 have been used as a component of Michael addition with equimolar amounts of 2-aminopyridine/2-am
A study on the reaction of 1,3-indandione with Schiff bases: Synthesis of new 1,3-indandiones with expected psychopharmacological and anticoagulant activity
Afsah,Etman,Hamama,Sayed-Ahmed
, p. 244 - 248 (2007/10/03)
Condensation of the title compound 1 with aldimines gave the 2-arylidene derivatives 3-9 instead of the expected Mannich bases 2. Compounds 10-11 were obtained from 1 and aldimines of α-ketoaldehydes. Isatin-anil (12) reacts with 1 to give 13. However, th
