Sulfonated polyethylene glycol (PEG-OSO 3 H) as a polymer supported biodegradable and recyclable catalyst in green organic synthesis: recent advances
The objective of this review is to summarize some of the recent advances in a sulfuric acid-
modified polyethylene glycol 6000 (PEG-OSO3H) as a stable, recyclable and bio …
modified polyethylene glycol 6000 (PEG-OSO3H) as a stable, recyclable and bio …
Synthesis, crystal structure and anti-inflammatory properties of curcumin analogues
G Liang, S Yang, H Zhou, L Shao, K Huang… - European journal of …, 2009 - Elsevier
Curcuminoids have been reported to possess multifunctional bioactivities, especially the
ability to inhibit proinflammatory induction. Since it has been suggested that the seven …
ability to inhibit proinflammatory induction. Since it has been suggested that the seven …
A Facile Solvent Free Claisen-Schmidt Reaction: Synthesis of α,α′-bis-(Substituted-benzylidene)cycloalkanones and α,α′-bis-(Substituted-alkylidene) …
Solvent-free Claisen-Schmidt reactions of cycloalkanones with various substituted
benzaldehydes (aryl aldehydes) using solid NaOH (20 mol%) and applying a grinding …
benzaldehydes (aryl aldehydes) using solid NaOH (20 mol%) and applying a grinding …
BF3.SiO2: An efficient heterogeneous alternative for regio-chemo and stereoselective claisen-schmidt condensation
B Sadeghi, BF Mirjalili, MM Hashemi - Journal of the Iranian Chemical …, 2008 - Springer
Iranian Chemical Society BF3.SiO2: An Efficient Heterogeneous Alternative for Regio-Chemo
and Stereoselective Claisen-Schmidt Page 1 J. Iran. Chem. Soc., Vol. 5, No. 4, December 2008 …
and Stereoselective Claisen-Schmidt Page 1 J. Iran. Chem. Soc., Vol. 5, No. 4, December 2008 …
Green, rapid, and highly efficient syntheses of α,α′‐bis[(aryl or allyl)idene]cycloalkanones and 2‐[(aryl or allyl)idene]‐1‐indanones as potentially biologic compounds via …
R Bakhshi, B Zeynizadeh… - Journal of the Chinese …, 2020 - Wiley Online Library
A new, green, and highly efficient protocol for the expeditious preparation of some α, α′‐bis
[(aryl or allyl) idene] cycloalkanones and 2‐[(aryl or allyl) idene]‐1‐indanones via a simple …
[(aryl or allyl) idene] cycloalkanones and 2‐[(aryl or allyl) idene]‐1‐indanones via a simple …
A bis-indole/carbazole based C5-curcuminoid fluorescent probe with large Stokes shift for selective detection of biothiols and application to live cell imaging
A series of heterocyclic C5-curcuminoids (bis (arylmethylidene) acetones)(PJ1–PJ6) having
a large Stokes shift (Δλ= 104–173 nm) have been synthesized for the selective detection of …
a large Stokes shift (Δλ= 104–173 nm) have been synthesized for the selective detection of …
Highly selective Claisen–Schmidt condensation catalyzed by silica chloride under solvent-free reaction conditions
H Hazarkhani, P Kumar, KS Kondiram… - Synthetic …, 2010 - Taylor & Francis
Full article: Highly Selective Claisen–Schmidt Condensation Catalyzed by Silica Chloride Under
Solvent-Free Reaction Conditions Skip to Main Content Taylor and Francis Online homepage …
Solvent-Free Reaction Conditions Skip to Main Content Taylor and Francis Online homepage …
New observation on a class of old reactions: Chemoselectivity for the solvent-free reaction of aromatic aldehydes with alkylketones catalyzed by a double-component …
ZX Shan, XX Luo, L Hu, XY Hu - Science China Chemistry, 2010 - Springer
Solvent-free reactions of aromatic aldehydes with three representative ketones, including
acetophenone, acetone and cyclohexanone, have been examined under the catalysis of a …
acetophenone, acetone and cyclohexanone, have been examined under the catalysis of a …
Monocarbonyl analogs of curcumin based on the pseudopelletierine scaffold: synthesis and anti-inflammatory activity
D Pawelski, A Walewska, S Ksiezak… - International Journal of …, 2021 - mdpi.com
Curcumin (CUR) is a natural compound that exhibits anti-inflammatory, anti-bacterial, and
other biological properties. However, its application as an effective drug is problematic due …
other biological properties. However, its application as an effective drug is problematic due …
Structure activity relationship of arylidene pyrrolo and pyrido [2, 1-b] quinazolones as cytotoxic agents: synthesis, SAR studies, biological evaluation and docking …
Tubulin is the one of the most useful and strategic molecular targets for anticancer drugs.
Agents that bind in Colchicine-binding site of tubulin include Phenstatin, Combretastatin A-4 …
Agents that bind in Colchicine-binding site of tubulin include Phenstatin, Combretastatin A-4 …