Microwave assisted aminocatalyzed [3 + 2] annulation between α-iminonitriles and succinaldehyde: synthesis of pyrrole-3-methanols and related polycyclic ring systems

RSC Advances ◽  
2016 ◽  
Vol 6 (46) ◽  
pp. 39741-39749 ◽  
Author(s):  
Nisar A. Mir ◽  
Sachin Choudhary ◽  
Panduga Ramaraju ◽  
Deepika Singh ◽  
Indresh Kumar
Keyword(s):  
Microwave Irradiation ◽  
Efficient Method ◽  
Ring Systems ◽  
Microwave Assisted ◽  
Highly Efficient ◽  
High Yields

A quick and highly efficient method for the synthesis of substituted pyrrole-3-methanols from α-iminonitriles and succinaldehyde under microwave irradiation is reported with good to high yields (up to 75%).

scholarly journals Microwave Assisted Synthesis of 1,5-Benzothiazepines Using Greener Reaction Medium

2019 ◽  
Vol 31 (5) ◽  
pp. 993-996 ◽  
Author(s):  
Sanjay S. Kotalwar ◽  
Amol D. Kale ◽  
Ram B. Kohire ◽  
Vasant B. Jagrut
Keyword(s):  
Reaction Time ◽  
Microwave Irradiation ◽  
Reaction Medium ◽  
Microwave Assisted Synthesis ◽  
Reaction Conditions ◽  
Renewable Sources ◽  
Microwave Assisted ◽  
High Yields

An efficient and eco-friendly synthesis of 1,5-benzothiazepines has been developed by the reaction of various 2-propen-1-ones with 2-aminothiophenol using microwave irradiation in greener reaction medium, glycerol. The clean reaction conditions, shorter reaction time, high yields and non-toxic, biodegradable reaction medium manufactured from renewable sources are unique features of this method.

Microwave-assisted palladium mediated efficient synthesis of pyrazolo[3,4-b]pyridines, pyrazolo[3,4-b]quinolines, pyrazolo[1,5-a]pyrimidines and pyrazolo[1,5-a]quinazolines

RSC Advances ◽  
2014 ◽  
Vol 4 (46) ◽  
pp. 24001-24006 ◽  
Author(s):  
Kommuri Shekarrao ◽  
Partha Pratim Kaishap ◽  
Venkateshwarlu Saddanapu ◽  
Anthony Addlagatta ◽  
Sanjib Gogoi ◽  
...  
Keyword(s):  
Microwave Irradiation ◽  
Efficient Method ◽  
Solvent Free ◽  
Efficient Synthesis ◽  
Aryl Aldehydes ◽  
Microwave Assisted ◽  
Fused Heterocycles ◽  
Palladium Catalyzed ◽  
Solvent Free Reaction

An efficient method was developed for the synthesis of pyrazole fused heterocycles via the palladium-catalyzed solvent free reaction of β-halovinyl/aryl aldehydes and 3-aminopyrazoles/5-aminopyrazoles under microwave irradiation in good yields.

scholarly journals On water catalyst-free synthesis of benzo[d]imidazo[2,1-b] thiazoles and novel N-alkylated 2-aminobenzo[d]oxazoles under microwave irradiation

RSC Advances ◽  
2020 ◽  
Vol 10 (2) ◽  
pp. 770-778 ◽  
Author(s):  
Narasimharao Mukku ◽  
Barnali Maiti
Keyword(s):  
Microwave Irradiation ◽  
Microwave Assisted ◽  
Catalyst Free ◽  
Highly Efficient

A highly efficient unprecedented catalyst-free microwave-assisted procedure for synthesizing benzo[d]imidazo[2,1-b]thiazoles and N-alkylated 2-aminobenzo[d]oxazol in green media was developed.

scholarly journals Microwave-assisted urea catalyzed Knoevenagel condensation of aldehydes with active methylene compounds

2020 ◽  
Vol 55 (2) ◽  
pp. 159-164
Author(s):  
WT Purba ◽  
PS Roy ◽  
S Jannat ◽  
SA Begum ◽  
MM Rahman
Keyword(s):  
Microwave Irradiation ◽  
Efficient Method ◽  
Knoevenagel Condensation ◽  
Efficient Catalyst ◽  
Microwave Assisted ◽  
Solvent Free Conditions ◽  
Wide Range ◽  
Active Methylene Compounds ◽  
Reaction Proceeds ◽  
Active Methylene

Rapid and efficient method for the synthesis of substituted olefins such as 2-(4-chlorophenylmethylene) malononitrile, 2-(4-hydroxyphenylmethylene) malononitrile and 2-cyano-3-(4-hydroxyphenyl) acrylamide etc under the influence of microwave irradiation are described. Urea has been utilized as an efficient catalyst for the Knoevenagel condensation of aldehydes with acidic active methylene compounds such as malononitrile, ethylcyanoacetate and cyanoacetamide to afford substituted olefins under the influence of microwave irradiation. The reaction proceeds smoothly under mild and solvent free conditions and the products are obtained in good yield. The method is applicable for a wide range of aldehydes including aromatic and heterocyclic substrates. Bangladesh J. Sci. Ind. Res.55(2), 159-164, 2020

A One-Pot, Three-Component, Solvent-Free Synthesis of Novel 6H-Chromeno[3’,4’:5,6]Pyrido[2,3-d]Pyrimidine-Triones under Microwave Irradiation

2018 ◽  
Vol 42 (12) ◽  
pp. 604-607
Author(s):  
Loghman Firoozpour ◽  
Hoda Yahyavi ◽  
Ramona Ejtemaei ◽  
Setareh Moghimi ◽  
Alireza Foroumadi
Keyword(s):  
Microwave Irradiation ◽  
Efficient Method ◽  
Barbituric Acid ◽  
Reaction Times ◽  
Solvent Free ◽  
One Pot ◽  
Solvent Free Conditions ◽  
Substituted Benzaldehydes ◽  
High Yields ◽  
Solvent Free Synthesis

A green and efficient method for preparing novel heterocyclic systems is established through the reaction of differently substituted benzaldehydes, barbituric acid and 4-amino-2H-chromene-2-one under solvent-free conditions. This method affords 6H-chromeno[3’,4’:5,6] pyrido[2,3-d]pyrimidine-trione derivatives in high yields and short reaction times.

Solvent-Free, Microwave-Assisted Conversion of Tosylates into Iodides

2014 ◽  
Vol 67 (9) ◽  
pp. 1360 ◽  
Author(s):  
Jia Cao ◽  
Patrick Perlmutter
Keyword(s):  
Efficient Method ◽  
Sodium Iodide ◽  
Reaction Times ◽  
Solvent Free ◽  
Microwave Cavity ◽  
Microwave Assisted ◽  
Crude Product ◽  
In Situ Generation ◽  
High Yields

A highly efficient method for the conversion of primary tosylates into the corresponding iodides is outlined. The method involves heating a neat mixture of the tosylate and solid sodium iodide in a microwave cavity. Reaction times are short, usually about 60 minutes, delivering high yields. This procedure is especially useful for the in situ generation of volatile primary iodides, and for most of the primary iodides, the crude product is sufficiently pure.

The Synthesis of α-Hydroxyphosphonates Mediated by Microwave Irradiation under Solvent-Free Conditions

2002 ◽  
Vol 2002 (6) ◽  
pp. 291-292 ◽  
Author(s):  
Babak Kaboudin ◽  
Rahman Nazari
Keyword(s):  
Microwave Irradiation ◽  
Efficient Method ◽  
Solvent Free ◽  
Microwave Assisted ◽  
Solvent Free Conditions

Microwave-assisted hydrophosphonylation of aldehydes under solvent-free conditions was found to be an efficient method for the preparation of α-hydroxyphosphonates; the method was reliable, efficient and high yielding.

Microwave-Assisted Efficient synthesis of Dihydro Pyrimidines: Improved High Yielding Protocol for the Biginelli Reaction

2000 ◽  
Vol 2000 (7) ◽  
pp. 354-355 ◽  
Author(s):  
J.S. Yadav ◽  
B.V. Subba Reddy ◽  
E. Jagan Reddy ◽  
T. Ramalingam
Keyword(s):  
Acetic Acid ◽  
Microwave Irradiation ◽  
Biginelli Reaction ◽  
Acid Catalysts ◽  
Efficient Synthesis ◽  
One Pot ◽  
Amberlyst 15 ◽  
Microwave Assisted ◽  
Cyclocondensation Reaction ◽  
High Yields

Dihydropyrimidines were synthesised in high yields by one-pot cyclocondensation reaction of aldehydes, aceto-acetates and urea using various acid catalysts like Amberlyst-15, Nafion-H, KSF clay and dry acetic acid under microwave irradiation.

scholarly journals Microwave-Assisted Three-Component “Catalyst and Solvent-Free” Green Protocol: A Highly Efficient and Clean One-Pot Synthesis of Tetrahydrobenzo[b]pyrans

2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Sougata Santra ◽  
Matiur Rahman ◽  
Anupam Roy ◽  
Adinath Majee ◽  
Alakananda Hajra
Keyword(s):  
Knoevenagel Condensation ◽  
One Pot ◽  
Green Protocol ◽  
Microwave Assisted ◽  
Highly Efficient ◽  
One Pot Synthesis ◽  
Purification Technique ◽  
The One ◽  
High Yields ◽  
Operational Simplicity

A green and highly efficient method has been developed for the one-pot synthesis of tetrahydrobenzo[b]pyrans via a three-component condensation of aldehydes, 1,3-cyclic diketones, and malononitrile under MW irradiation without using any catalyst and solvent. This transformation presumably occurs by a sequential Knoevenagel condensation, Michael addition, and intramolecular cyclization. Operational simplicity, solvent and catalyst-free conditions, the compatibility with various functional groups, nonchromatographic purification technique, and high yields are the notable advantages of this procedure.

Squaramide-Catalyzed Asymmetric Michael/Cyclization Cascade Reaction of Unsaturated Thiazolidinones and 3-Isothiocyanato Oxindoles: Synthesis of New Bispirocyclic Heterocycles

Synthesis ◽  
2018 ◽  
Vol 50 (07) ◽  
pp. 1535-1545 ◽  
Author(s):  
Da-Ming Du ◽  
Yong-Xing Song
Keyword(s):  
Efficient Method ◽  
Cascade Reaction ◽  
Reaction Conditions ◽  
Highly Efficient ◽  
Chiral Centers ◽  
High Yields

A highly efficient method for the construction of oxindole-pyrrolidone-thiazolidinone bispirocyclic heterocycles bearing three contiguous chiral centers including two quaternary one via a Michael/cyclization cascade reaction has been developed. Using bifunctional cinchona-derived squaramide as catalyst, the reactions of 3-isothio­cyanato oxindoles with unsaturated thiazolidinone derivatives proceeded smoothly under mild reaction conditions to afford a series of complex chiral oxindole-pyrrolidone-thiazolidinone bispirocyclic heterocycles in high yields (up to 99%) with excellent diastereo- and enantioselectivities (up to >99:1 dr, >99% ee).

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