A Novel and Highly Efficient Method for the Direct Conversion of Aryl Aldehyde Bisulfite Adducts to Their Aryl Trimethylsilyl Ethers in a One-Pot Manner Catalyzed by Montmorillonite K-10.

ChemInform ◽  
2006 ◽  
Vol 37 (19) ◽  
Author(s):  
Mohammad M. Khodaei ◽  
Ahmad R. Khosropour ◽  
Jamshide Abbasi
RSC Advances ◽  
2019 ◽  
Vol 9 (66) ◽  
pp. 38877-38881 ◽  
Author(s):  
Hangkong Yuan ◽  
Bright T. Kusema ◽  
Zhen Yan ◽  
Stéphane Streiff ◽  
Feng Shi

A simple and highly efficient method was developed for one pot transformation of 5-(hydroxymethyl)furfural (5-HMF) into 2,5-bis(aminomethyl)furan (BAF) over bifunctional Cu4Ni1Al4Ox catalyst using two-stage reaction process, affording the BAF in 85.9% yield.


2013 ◽  
Vol 2013 ◽  
pp. 1-5 ◽  
Author(s):  
Shubha Jain ◽  
Deepika Rajguru ◽  
Balwant S. Keshwal ◽  
Aman D. Acharya

A rapid, clean, and highly efficient method for synthesis of dihydropyrano[3,2-c]chromene derivatives by one-pot, three-component condensation of aromatic aldehydes, malononitrile, and 4-hydroxycoumarin using DABCO as catalyst in solvent-free neat conditions is described. The present method has the advantages of mild reaction conditions, short reaction times, easy isolation of products, and excellent yields.


RSC Advances ◽  
2015 ◽  
Vol 5 (36) ◽  
pp. 28163-28170 ◽  
Author(s):  
Shivam Bajpai ◽  
Sundaram Singh ◽  
Vandana Srivastava

A highly efficient method for the synthesis of substituted imidazoles from a multicomponent reaction of isatin derivatives with ammonium acetate and aromatic aldehydes under solvent-free conditions has been established.


RSC Advances ◽  
2014 ◽  
Vol 4 (50) ◽  
pp. 26301-26308 ◽  
Author(s):  
Shakil N. Afraj ◽  
Chinpiao Chen ◽  
Gene-Hsian Lee

A one-pot green and highly efficient method for the synthesis of propargylamines and distereoselective synthesis of fused triazoles via three-component coupling in the presence of manganese(ii) chloride and a catalyst-free 1,3-dipolar cycloaddition reaction without using a co-catalyst is reported.


Synthesis ◽  
2017 ◽  
Vol 50 (02) ◽  
pp. 341-348 ◽  
Author(s):  
Jianhui Liu ◽  
Xiangting Min ◽  
Yawen Dong ◽  
Mustafa Hussain

A novel, simple, and highly efficient method has been designed for the synthesis of ω-substituted arylbiurets in a one-pot reaction. The primary features of this protocol include readily available starting materials, an easy work-up procedure, and yields of 51 to 87%. ω-Substituted arylbiurets can be selectively prepared with an excess of potassium cyanate (KOCN). However, use of an excess of glacial acetic acid (AcOH) switches the reaction towards the formation of N-monosubstituted urea.


Synlett ◽  
2017 ◽  
Vol 28 (14) ◽  
pp. 1807-1810 ◽  
Author(s):  
Ruotian Tang ◽  
Chunfeng Jiang ◽  
Hongliang Li ◽  
Wei Li ◽  
Youjun Xu

A novel synthesis of N-substituted 4-​amino-​6-​methyl resorcinols from polysubstituted cyclohexanone was developed. The reaction was performed in an easy ‘one-pot’, tandem manner with well-tolerated substituent on the nitrogen to give the desired compound in good to excellent yield. This highly efficient method will find broad application in the synthesis of some natural products and bioactive interesting compounds.


RSC Advances ◽  
2015 ◽  
Vol 5 (87) ◽  
pp. 71071-71075 ◽  
Author(s):  
Xin Huang ◽  
Kenny Pham ◽  
Xiaofeng Zhang ◽  
Wen-Bin Yi ◽  
Jeremy H. Hyatt ◽  
...  

A highly efficient method for asymmetric synthesis of fluorinated 2-piperidinones bearing four stereogenic centres is introduced.


2013 ◽  
Vol 10 (10) ◽  
pp. 764-769 ◽  
Author(s):  
Akbar Mobinikhaledi ◽  
Alireza Amiri

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