Manganese(ii) chloride catalyzed highly efficient one-pot synthesis of propargylamines and fused triazoles via three-component coupling reaction under solvent-free condition

RSC Advances ◽  
2014 ◽  
Vol 4 (50) ◽  
pp. 26301-26308 ◽  
Author(s):  
Shakil N. Afraj ◽  
Chinpiao Chen ◽  
Gene-Hsian Lee
Keyword(s):  
Efficient Method ◽  
Cycloaddition Reaction ◽  
Coupling Reaction ◽  
Dipolar Cycloaddition ◽  
One Pot ◽  
Co Catalyst ◽  
Free Condition ◽  
Highly Efficient ◽  
Solvent Free Condition ◽  
Three Component Coupling

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 OF SOME PROPARGYLAMINES VIA A3 COUPLING REACTION

2020 ◽  
Vol 65 (10) ◽  
pp. 67-72
Author(s):  
Thanh Hoang Thi ◽  
Trang Tran Thi Thu ◽  
Hoan Duong Quoc
Keyword(s):  
Coupling Reaction ◽  
Solvent Free ◽  
One Pot ◽  
Free Condition ◽  
Highly Efficient ◽  
Solvent Free Condition ◽  
A3 Coupling

Condition for synthesis of propargylamines has been found in highly efficient as a one-pot multi-component protocol. Copper(I) iodide (30% mol) under solvent free condition gave propargylamine in good yields. Structures of propargylamines were elucidated with NMR, MS methods.

Sulfated polyborate: a new and eco-friendly catalyst for one-pot multi-component synthesis of 3,4-dihydropyrimidin-2(1H)-ones/thiones via Biginelli reaction

2016 ◽  
Vol 40 (12) ◽  
pp. 10412-10417 ◽  
Author(s):  
Chetan K. Khatri ◽  
Deelip S. Rekunge ◽  
Ganesh U. Chaturbhuj
Keyword(s):  
Biginelli Reaction ◽  
Solvent Free ◽  
Synthetic Methodology ◽  
One Pot ◽  
Free Condition ◽  
Sulfated Polyborate ◽  
Highly Efficient ◽  
Excellent Yield ◽  
Solvent Free Condition

A highly efficient and improved synthetic methodology for the preparation of 3,4-dihydropyrimidin-2(1H)-one derivatives in good to excellent yield via Biginelli reaction of β-ketoesters/β-diketone, urea/thiourea and various aldehydes using new, efficient and recyclable sulfated polyborate catalyst under the solvent-free condition is reported.

A Simple and Economic Synthesis of Propargylamines by CuI-Catalyzed Three-Component Coupling Reaction with Succinic Acid as Additive

2009 ◽  
Vol 62 (1) ◽  
pp. 75 ◽  
Author(s):  
Gerui Ren ◽  
Jinli Zhang ◽  
Zheng Duan ◽  
Mengjun Cui ◽  
Yangjie Wu
Keyword(s):  
Succinic Acid ◽  
Efficient Method ◽  
Coupling Reaction ◽  
One Pot ◽  
Wide Range ◽  
High Yields ◽  
Three Component Coupling

A practical and efficient method was developed for the synthesis of propargylamines in a one-pot procedure from aldehydes, amines, and alkynes by using CuI as catalyst and succinic acid as additive. By using this protocol, a wide range of propargylamines was obtained in high yields.

Catalysis by metal–organic frameworks: proline and gold functionalized MOFs for the aldol and three-component coupling reactions

RSC Advances ◽  
2014 ◽  
Vol 4 (25) ◽  
pp. 13093-13107 ◽  
Author(s):  
Liu Lili ◽  
Zhang Xin ◽  
Rang Shumin ◽  
Yang Ying ◽  
Dai Xiaoping ◽  
...  
Keyword(s):  
Aldol Reaction ◽  
Metal Organic Frameworks ◽  
Coupling Reaction ◽  
Coupling Reactions ◽  
One Pot ◽  
Postsynthetic Modification ◽  
Highly Efficient ◽  
Synthetic Strategy ◽  
Metal Organic ◽  
Three Component Coupling

Homochiral MOFs were engineered using postsynthetic modification and a one-pot synthetic strategy. l-Proline functionalized IRMOF-3 show high ee for aldol reaction. Gold functionalized CUP-1 catalysts are highly efficient for the A3 coupling reaction.

Copper-catalyzed Convenient Synthesis and SAR Studies of Substituted-1,2,3-triazole as Antimicrobial Agents

2018 ◽  
Vol 16 (1) ◽  
pp. 3-10
Author(s):  
Aniket P. Sarkate ◽  
Kshipra S. Karnik ◽  
Pravin S. Wakte ◽  
Ajinkya P. Sarkate ◽  
Ashwini V. Izankar ◽  
...  
Keyword(s):  
Antimicrobial Activity ◽  
Antifungal Activity ◽  
Antimicrobial Agents ◽  
Cycloaddition Reaction ◽  
Dipolar Cycloaddition ◽  
One Pot ◽  
Triazole Derivatives ◽  
Sar Studies ◽  
Convenient Synthesis ◽  
Antibacterial And Antifungal

Background:A novel copper-catalyzed synthesis of substituted-1,2,3-triazole derivatives has been developed and performed by Huisgen 1,3-dipolar cycloaddition reaction of azides with alkynes. The reaction is one-pot multicomponent.Objective:We state the advancement and execution of a methodology allowing for the synthesis of some new substituted 1,2,3-triazole analogues with antimicrobial activity.Methods:A series of triazole derivatives was synthesized by Huisgen 1,3-dipolar cycloaddition reaction of azides with alkynes. The structures of the synthesized compounds were elucidated and confirmed by 1H NMR, IR, MS and elemental analysis. All the synthesized compounds were tested for their antimicrobial activity against a series of strains of Bacillus subtilis, Staphylococcus aureus and Escherichia coli for antibacterial activity and against the strains of Candida albicans, Aspergillus flavus and Aspergillus nigar for antifungal activity, respectively.Results and Conclusion:From the antimicrobial data, it was observed that all the newly synthesized compounds showed good to moderate level of antibacterial and antifungal activity.

Rapid Access to Novel 1,2,3-Triazolo-Heterocyclic Scaffolds via Tandem Knoevenagel Condensation/Azide–Alkyne 1,3-Dipolar Cycloaddition Reaction in One Pot

2014 ◽  
Vol 16 (9) ◽  
pp. 466-477 ◽  
Author(s):  
Ram Awatar Maurya ◽  
Praveen Reddy Adiyala ◽  
D. Chandrasekhar ◽  
Chada Narsimha Reddy ◽  
Jeevak Sopanrao Kapure ◽  
...  
Keyword(s):  
Knoevenagel Condensation ◽  
Cycloaddition Reaction ◽  
Dipolar Cycloaddition ◽  
One Pot ◽  
Rapid Access

scholarly journals Highly Efficient Acetalization and Ketalization Catalyzed by Cobaloxime under Solvent-Free Condition

Catalysts ◽  
2018 ◽  
Vol 8 (2) ◽  
pp. 48 ◽  
Author(s):  
Yang Zong ◽  
Liting Yang ◽  
Shanyu Tang ◽  
Longjia Li ◽  
Wanjie Wang ◽  
...  
Keyword(s):  
Solvent Free ◽  
Free Condition ◽  
Highly Efficient ◽  
Solvent Free Condition
Sign in / Sign up

Export Citation Format

Share Document