scholarly journals Efficient deprotection of F-BODIPY derivatives: removal of BF2 using Brønsted acids

2015 ◽  
Vol 11 ◽  
pp. 37-41 ◽  
Author(s):  
Mingfeng Yu ◽  
Joseph K-H Wong ◽  
Cyril Tang ◽  
Peter Turner ◽  
Matthew H Todd ◽  
...  

The effective and efficient removal of the BF2 moiety from F-BODIPY derivatives has been achieved using two common Brønsted acids; treatment with trifluoroacetic acid (TFA) or methanolic hydrogen chloride (HCl) followed by work-up with Ambersep® 900 resin (hydroxide form) effects this conversion in near-quantitative yields. Compared to existing methods, these conditions are relatively mild and operationally simple, requiring only reaction at room temperature for six hours (TFA) or overnight (HCl).

2016 ◽  
Vol 5 (4) ◽  
Author(s):  
Ramadan Ahmed Mekheimer ◽  
Abdullah Mohamed Asiri ◽  
Afaf Mohamed Abdel Hameed ◽  
Reham R. Awed ◽  
Kamal Usef Sadek

AbstractStarting from readily available 2-naphthol, aldehydes, aryl and alkylamines, a variety of Betti bases were efficiently synthesized utilizing a catalytic amount of cerium (IV) ammonium nitrate (CAN) at room temperature. This protocol has advantages of high yield, mild reaction conditions, no environmental pollution, diversity of reactants and simple work up procedure.


2020 ◽  
Vol 59 (42) ◽  
pp. 18781-18789
Author(s):  
Jinwei Chen ◽  
Meng Huang ◽  
Wang Chen ◽  
Haiyan Tang ◽  
Yi Jiao ◽  
...  

ACS Omega ◽  
2019 ◽  
Vol 4 (26) ◽  
pp. 21998-22007 ◽  
Author(s):  
Zhihua Xu ◽  
Gang Huang ◽  
Zhaoxiong Yan ◽  
Nenghuan Wang ◽  
Lin Yue ◽  
...  

2019 ◽  
Vol 31 (6) ◽  
pp. 1357-1361 ◽  
Author(s):  
NARENDRA R. KAMBLE ◽  
VINOD T. KAMBLE

A combinatorial library of benzylpyrazolyl coumarin derivatives have been synthesized by a green one-pot four-component reaction between aryl hydrazine/hydrazine hydrate (1), ethyl acetoacetate (2), aromatic aldehydes (3) and 4-hydroxycoumarin (4) catalyzed by niobium pentachloride with silver salt under solvent-free conditions has been developed. Experimental simplicity, simple work-up procedure and solvent-free reaction condition at room temperature are important features of the present protocol.


Catalysts ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 820
Author(s):  
Efraín Polo ◽  
Valentina Arce-Parada ◽  
Xaviera A. López-Cortés ◽  
Jesús Sánchez-Márquez ◽  
Alejandro Morales-Bayuelo ◽  
...  

A series of pyrazolo-fused 4-azafluorenones (indeno[1,2-b]pyrazolo[4,3-e]pyridines, IPP) were synthesized via the three-component reaction between arylaldehydes, 3-methyl-1H-pyrazol-5-amine and 1,3-indanedione in an ionic liquid as a catalyst at room temperature. The applied synthetic route has the advantages of easy work-up under mild reaction conditions presenting moderate yields and an environmentally benign procedure. A theoretical study based on conceptual-density functional theory has been done, bond reactivity indices have been calculated and an electrophilic and nucleophilic character of localized orbitals has been determined to analyze the possible electronic mechanisms.


2013 ◽  
Vol 66 (6) ◽  
pp. 661 ◽  
Author(s):  
Prashant B. Thorat ◽  
Santosh V. Goswami ◽  
Wamanrao N. Jadhav ◽  
Sudhakar R. Bhusare

We report an enantioselective Henry (nitroaldol) reaction catalysed by an organocatalyst using water as solvent. The enantioselective synthesis of β-nitroalcohols was achieved by using a neutral chiral organocatalyst, through strong hydrogen bonding, which results in the formation of corresponding products in excellent yield and enantioselectivity at room temperature. Other attractive features of the method are the eco-friendly, non-hazardous, and mild reaction conditions, inexpensive catalyst, and simple work up conditions.


2011 ◽  
Vol 76 (9) ◽  
pp. 1191-1198 ◽  
Author(s):  
Bahador Karami ◽  
Saeed Khodabakhshi

Convenient and simple procedures for the synthesis of phenazine and quinoxaline derivatives were developed via a reaction of ophenylenediamines and 1,2-dicarbonyl compounds. In addition, the synthesis of two new derivatives of 1,4-benzo diazine derivatives and the catalytic activity of magnesium sulfate heptahydrate (MgSO4?7H2O) in the room temperature condensation of o-phenylenediamines and 1,2- dicarbonyl compounds in ethanol as solvent are reported. This method has many appealing attributes, such as excellent yields, short reactions times, and simple work-up procedures.


2015 ◽  
Vol 69 (3) ◽  
Author(s):  
Hamed Rouhi-Saadabad ◽  
Batool Akhlaghinia

AbstractAn efficient mixed reagent for direct synthesis of symmetrical carboxylic anhydrides from carboxylic acids has been prepared. Carboxylic acids are converted to anhydrides using triphenylphosphine/ trichloroisocyanuric acid under mild reaction conditions at room temperature. Short reaction time, excellent yields of products, low cost, availability of reagents, simple experimental procedure, and easy work-up of the products are the main advantages of the presented method.


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