Microwave chemistry, recent advancements, and eco-friendly microwave-assisted synthesis of nanoarchitectures and their applications: a review

Microwave Chemistry ◽

Microwave Assisted ◽

Promising Area

In the Conventional laboratory or industry heating technique involve Bunsen burner, heating mental/hot plates and electric heating ovens. To produce a variety of useful compounds for betterment of mankind, the Microwave Chemistry was introduced in year 1955 and finds a place in one of the Green chemistry method. In Microwave chemistry is the science of applying microwave radiation to chemical reactions. Microwaves act as high frequency electric fields and will generally heat any material containing mobile electric charges, such as polar molecules in a solvent or conducting ions in a solid. Polar solvents are heated as their component molecules are forced to rotate with the field and lose energy in collisions i.e. the dipole moments of molecules are important in order to proceed with the chemical reactions in this method. It can be termed as microwave-assisted organic synthesis (MAOS), Microwave-Enhanced Chemistry (MEC) or Microwave-organic Reaction Enhancement synthesis (MORE). Microwave-Assisted Syntheses is a promising area of modern Green Chemistry could be adopted to save the earth.

Microwave-assisted synthesis of Cd (II) complex of 4-pyridinecarboxaldehyde thiosemicarbazone

10.3390/ecsoc-17-c007 ◽

2013 ◽

Author(s):

Azadeh Tadjarodi ◽

Homayoun Gholipour

Keyword(s):

Conventional and Microwave Assisted Synthesis with Antimicrobial Evaluation of Novel Pyrrolidine Molecule: An Approach to Easy Synthetic Pathway

Journal of Chemistry and Chemical Sciences ◽

10.29055/jccs/585 ◽

2018 ◽

Vol 8 (2) ◽

pp. 298-303

Author(s):

K Sreekanth ◽

Anjali Jha

Keyword(s):

Synthetic Pathway ◽

Microwave Assisted ◽

Antimicrobial Evaluation

Microwave Assisted Synthesis of Cationic Amino Sugar Surfactants

Tenside Surfactants Detergents ◽

10.3139/113.110684 ◽

2020 ◽

Vol 57 (3) ◽

pp. 265-272

Author(s):

Priya S. Singh ◽

Aizaz Shaikh ◽

Aditi Deshmukh ◽

Amit P. Pratap

Keyword(s):

Amino Sugar ◽

MICROWAVE ASSISTED SYNTHESIS, QSAR AND MOLECULAR DOCKING STUDIES OF 2,4- THIAZOLIDINEDIONE DERIVATIVES

RASAYAN Journal of Chemistry ◽

10.31788/rjc.2019.1235165 ◽

2019 ◽

Vol 12 (03) ◽

pp. 1063-1071

Author(s):

B . Geetha ◽

G . Swarnalatha ◽

G.V . Subba Reddy

Keyword(s):

Molecular Docking ◽

Docking Studies ◽

Molecular Docking Studies ◽

Efficient One-pot microwave-assisted Synthesis and Spectroscopic Characterization of Novel Antitumor and Antimicrobial Hydroxypyrrolidin2-ones

Journal of Scientific Research in Science ◽

10.21608/jsrs.2018.15776 ◽

2018 ◽

Vol 35 (part 1) ◽

pp. 1-16

Author(s):

Eman Azmy ◽

Boshra Awad ◽

Halima Hefni ◽

Hanaa Saad ◽

Affaf Eltoukhy ◽

...

Keyword(s):

Spectroscopic Characterization ◽

One Pot ◽

Pyrrole: Chemical Synthesis, Microwave Assisted Synthesis, Reactions and Applications: A Review

Current Organic Chemistry ◽

10.2174/13852728113179990040 ◽

2013 ◽

Vol 17 (20) ◽

pp. 2279-2304 ◽

Cited By ~ 64

Author(s):

Shrinivas Joshi ◽

Uttam More ◽

Venkatrao Kulkarni ◽

Tejraj Aminabhavi

Keyword(s):

Chemical Synthesis ◽

Microwave Assisted ◽

Synthesis Reactions

Microwave assisted synthesis of novel Pyrazole derivatives and their biological evaluation as anti-bacterial agents

Combinatorial Chemistry & High Throughput Screening ◽

10.2174/1386207323666201019152206 ◽

2020 ◽

Vol 23 ◽

Author(s):

Hadis Khodadad ◽

Farhad Hatamjafari ◽

Khalil Pourshamsian ◽

Babak Sadeghi

Keyword(s):

Antibacterial Activity ◽

Aromatic Aldehydes ◽

Catalytic Amount ◽

Antibacterial Activities ◽

Structural Features ◽

Biological Evaluation ◽

Aureus Strain ◽

Pyrazole Derivatives ◽

Aim and Objective: Microwave-assisted condensation of acetophenone 1 and aromatic aldehydes 2 gave chalcone analogs 3, which were cyclized to pyrazole derivatives 6a-f via the reaction with hydrazine hydrate and oxalic acid in the presence of the catalytic amount of acetic acid in ethanol. Materials and Methods: The structural features of the synthesized compounds were characterized by melting point, FT-IR, 1H, 13C NMR and elemental analysis. Results: The antibacterial activities of the synthesized pyrazoles was evaluated against three gram-positive bacteria such as Enterococcus durans, Staphylococcus aureus, Bacillus subtilis and two gram-negative bacteria such as Escherichia coli and Salmonella typhimurium. Conclusion: All the synthesized pyrazoles showed relatively high antibacterial activity against S. aureus strain and none of them demonstrated antibacterial activity against E. coli.