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Abstract

On this assessment we provide an explanation for all of the specific statistics about Microwave assisted synthesis. Now a days the Microwave very much useful in to Microwave assisted synthesis reaction for inexperienced chemistry paintings through the various reactions. This is to begin with used by the shop energy and charge of response is fast. Microwave synthesis able to predicting many properties and fee of synthesis reaction is speedy in small time frame to get from product. All kind chemical response synthesis is also carried out by means of this microwave. Various authors’ words on their subject by means of the usage of this Microwave assisted synthesis. I display interest into microwave due to this is very useful for acting synthesis of response. In microwave numerous principals are added and this can be beneficial or beneficial to guide scientist.

Keywords

Microwave assisted synthesis, Green chemistry, Microwave, Heterocyclic.

Introduction

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Microwave chemistry involves the utilization of microwave radiation to facilitate chemical reactions. Conventional organic synthesis strategies face severa demanding situations, which include the immoderate use of luxurious raw substances, widespread time requirements, and, most critically, sizable chemical waste that contributes to disburden. For hundreds of years, traditional heating techniques, along with Bunsen burners, oil baths, and warm mantles, were hired to behavior chemical reactions. those techniques aren't most effective exertions-in depth and time- eating however  also  in efficient  in  terms  of  energy  and resource use . Additionally, they generate hot surfaces on response vessels, leading to the decomposition of reagents over time and the formation of poisonous byproducts. The reliance on solvents in those strategies in addition complicates subjects, as many solvents are risky to each health and the surroundings, necessitating additional healing strategies.  The restrictions  of  conventional  heating  strategies  can  be  addressed  through  alternative  strategies,  with  microwave  generation  being  a   distinguished  instance.   The pursuit of recent  synthetic  pathways  for  compound  synthesis  remains  a  big  and  challenging  goal  for  synthetic  chemists .  whether or not through  big  scale  or  small scale  efforts ,  the  search  for  an  ideal  artificial  direction one which  minimizes  environmental  impact  and  decreases  synthesis  charges  affords  substantial  clinical  and  highbrow  challenges,  requiring  meticulous  strategic  planning.  Consequently, a diffusion of techniques is presently being explored to sell green chemistry in research endeavors. The microwave-assisted natural  synthesis  approach  has  established  the  capacity  to  beautify the efficiency of chemical reactions by way of  growing  velocity,  enhancing  yields,  reducing  by products, and  generating  purer  desired  merchandise  in  a  cleanser  way.  This method  gives  several  benefits  over  conventional  techniques,  as   microwave heating selectively  targets  the reaction  mixture  without  heating  the  entire  surface  of  the  appliance,  in  contrast  to  conventional  strategies  that  rely  upon conduction to heat the mixture. This technique minimizes the advent of unwanted by products,  thereby  improving  yield  and  making  sure  a  greater  green  synthesis  manner . moreover,  it  circumvents the need  for  large  portions  of  harmful  organic solvents, a drawback regularly encountered in conventional synthesis methods. Those characteristics position microwave assisted synthesis as a prime instance of green chemistry.  Green chemistry, additionally known as "environmentally benign chemistry," is an emerging subject that emphasizes the 4 R's: Reuse, reduce, Recycling, and restoration. The number one goal of inexperienced chemistry is to minimize the reliance on toxic solvents and cast off  the  use  of  unsafe  substances  in  chemical  synthesis.  Regularly termed sustainable, it embodies a philosophy in chemical research and engineering that advocates for the design of merchandise and methods aimed at  decreasing  the  use  and  generation  of  dangerous  substances  in  experienced chemistry is predicated on using environmentally   pleasant substances to prevent the introduction of dangerous waste. Horvath et al. have characterized sustainable chemistry because the precept  that  resources,  along  with  strength,  ought  to  be  utilized  at  a  rate  that  allows  for  herbal  replenishment,  and  that  waste  technology  need  to  no  longer  exceed  the  fee  at  which  it  can  be  controlled.  In the 1990s,  Paul  Anastas  and  John C. Warner introduced twelve concepts of green chemistry, which advice for environmentally  responsible  practices  from the  preliminary  product  design  thru  to  its  synthesis ,  processing, evaluation, and eventual disposal.

A microwave is a form of electromagnetic strength that falls at the lower frequency of the electromagnetic spectrum inside the range of three hundred to three hundred, 000 MHz. within this area of electromagnetic strength simplest molecular rotation is affected no longer the molecular shape. However for their use in laboratory reactions, a frequency of 2.45 GHz is favored because it has the right penetration intensity for laboratory reaction conditions. Microwave (MW) radiation has widely been used in chemistry as an strength source due to the capability of particular compounds (solids or liquids) to convert electromagnetic power into  warmness.   Microwave   irradiation   has   several   benefits   over   traditional   heating   protocols,   which   include   homogeneous   and   rapid   heating   (excessive  internal  heating ),  mind  blowing   response   accelerations   because   of   the   heating   charge   (which  are  often  not  possible  to  replicate  with  conventional  heating ),  and   selective   heating

Applications Of Green Cheistry:

Microwave Assisted  organic  Synthesis  (MAOS)  is  identified  as  an  environmentally  pleasant  technology  because  of  its  large  applications  in  significantly  improving  numerous  natural  reactions. This technique  gets  rid  of  the  need  for  extended  heating,  resulting  in  high  yields  and  greater  selectivity,  while  also  generating  purifier  products.  Further ore, many natural reactions may be carried out without solvents.

III. Microwave Assisted Synthesis Uses:

MAOS has  emerged  as  a  essential  aid  for  chemists  searching  for  speedy  and  green  natural  synthesis. A giant body of studies on MAOS is available in each published works and patent literature.  Numerous  critiques,  several  books,  and  on-line  assets  offer  comprehensive  insights  into  this  subject  matter.  Microwaves  serve  as  a  warmness  source  for  chemical  synthesis,  and  it's  far  predicted  that   they will  end  up  the  important  heating  method  in  laboratories within the close to future. D. M. P. Mingos and associates have provided an in-depth  analysis  of  the  theoretical  principles underlying  microwave  dielectric  heating.  Gedye and  de  los  angeles  Hoz  have  explored  the  proposed  ‘unique microwave impact,’ even as Loupy and others have posted a couple of critiques on solvent-loose microwave-assisted reactions. Moreover, Strauss has documented organic synthesis carried out in high-temperature aqueous environments. these days, a take a look at mentioned on Microwave-Assisted Condensation Reactions concerning Acetophenone Derivatives and Activated Methylene Compounds with Aldehydes, catalyzed by way of Boric Acid below solvent-loose conditions. The synthesis of multi component compounds, along with 3-(4-Arylmethylamino) butyl-5-arylidene-rhodanines the  use  of  microwave  irradiation,  has  additionally  been  currently  documented. Microwaves are a form of electromagnetic radiation located on the lower frequency give up of the electromagnetic spectrum. This microwave location is placed among infrared radiation and radio frequencies, similar to wavelengths starting from 1 cm to one m (with frequencies from 30 GHz to 300 MHz, respectively). domestic and business microwave ovens normally function at frequencies of 2450 MHz (12.2 cm) or 900 MHz (33. three cm).

IV. Microwave Assisted Synthesis Of Heterocyclic Compounds:

Microwave chemistry is the technological know-how of applying microwave radiation to chemical reactions. Microwave synthesis represents a chief  step  forward  in  the  artificial  chemistry  methodology; a  dramatic  alternate  within  the  manner  chemical  synthesis  is  completed. Microwave assisted natural synthesis has revolutionized natural synthesis.  In evaluation to the number and variety of such heterocyclic compounds, the  variety  of  synthetic  methods  to  manage  to  pay  for  sulfur  and  nitrogen containing  molecules  is  in  exercise  constrained  to  the  supply  of  the  ideal  sulfur  or  nitrogen  reagent.  From time to time the education of those heterocyclic systems through conventional approaches is difficult  work  that  means  many  artificial  steps  and  vast  starting  material.  Due to those motives the various opportunities provided by means of the microwave generation are especially appealing in which speedy, high-yielding protocols and the avoidance or facilitation of purification is notably appropriate. Therefore, the prevailing literature survey consists of synthesis of heterocyclic nucleus based on microwaves.

V. Mechanism of Heat Generation by Microwaves:

1. Dipolar Polarization

The manner of heat era in microwave-assisted synthesis is typically attributed to dipolar polarization. When uncovered to microwave radiation, molecules that own a everlasting dipole  second  align  themselves  with  the  electric  subject  of  the  microwaves.  This alignment results in  molecular  oscillation  and  subsequent  collisions  a  number  of  the  molecules.  The friction generated from those oscillations out comes inside the production of warmth.  consequently, for a  reagent  to  be  microwave energetic,  it  should  have  a dipole  second  and  be  polarizable. The heating effect is  extra  mentioned  in  molecules  with  better  polarizability.  consequently, microwave  heating  is  effective  only  for  polar  materials  which  include  water,  methanol,  ethanol,  ammonia,  and  formic acid,  at  the  same  time  as  non-polar  molecules  do  now  not  interact  with  microwave  radiation.

2. Ionic Conduction

Ionic conduction includes the rapid superheating of ionic materials because of the motion of electrical costs whilst an electric powered field is implemented.  The  motion  of   ions  increases  the  rate  of  collisions,  changing  kinetic  energy  into  warmness.  Because the temperature rises, electricity transfer will become greener. Ionic drinks, specially, take in microwave radiation efficiently and facilitate rapid electricity transfer thru ionic conduction. For instance, when distilled water and tap water samples are heated in a unmarried-mode microwave cavity at a regular strength level for a fixed length, the tap water sample reaches a better final temperature. This phenomenon takes place because of the interplay of the electrical subject with the pattern, in which the heat generated from ionic conduction, due to the presence of ions, complements the heat produced thru dipolar polarization, ensuing in an accelerated final temperature in the faucet water.

3. Rapid Reaction Rates

Analysis of the prevailing experimental data  indicates  that  microwaves  can  enhance  heating fees  by  using a aspect of lots as compared to standard heating techniques. In a microwave reactor, the microwave energy supply does not come into direct contact with the sample being heated, ensuing within the speedy final touch of the response.

4. Interfacial Polarization

The interfacial polarization method can be considered as a combination of both the conduction and dipolar polarization mechanisms. It is important for heating systems that comprise a conducting material dispersed in a non-conducting material.

VI. Microwave Theory:

Microwave irradiation, running  at  a  frequency  of  two .forty  five  GHz  to  avoid  interference  with  telecommunications,  is  a  shape  of  electromagnetic  radiation  with  photon  energy  too  low  to  break  chemical  bonds  or  without  delay  set  off  chemical  reactions.  Instead, microwave superior chemistry relies on dielectric heating, wherein substances inclusive of solvents or reagents take in microwave electricity and convert it into warmth. This heating happens mostly via mechanisms: dipolar polarisation, wherein molecular dipoles attempt to align with the oscillating electric field and create warmth because of friction and dielectric loss; and ionic conduction, wherein charged debris oscillate and purpose heating thru collisions with neighboring molecules. The frequency used permits molecules enough time to in part align with the field, maximizing heat technology with out following the sphere flawlessly.

VII. Instrumentation:

Microwave-assisted synthesis is carried out inside specialized microwave reactors, which usually include  5  primary  components:  a  excessive  voltage  transformer, a magnetron, a waveguide, a cooling fan, and a cavity.

Two types of microwave reactors can be used in the laboratory:

1. Multimode Batch Reactors

2. Single Mode Instrument

High Voltage Transformer

A microwave reactor necessitates a excessive voltage deliver, normally starting from 3000 to 3400 V. To generate this voltage, a high voltage transformer is hired, making use of various capacitors to amplify the electric contemporary. This process guarantees that the reactor receives the essential power for its operation.

Magnetron

The magnetron is composed of essential elements: a vacuum tube and two ring-fashioned magnets that encircle the tube. The vacuum tube itself consists of a copper anode and a crucial filament crafted from tungsten and thorium. The magnetron receives excessive voltage from the transformer, converting microwave strength into thermal electricity by creating a diode that directs electrons via magnetic fields. the ring-formed magnets manual the electrons lower back to the crucial filament, resulting inside the generation of oscillating waves.

Waveguide

The number one function of the waveguide is to channel the waves produced by way of the magnetron in a selected path, functioning as a guiding conduit. it's miles built as a hole metallic tube with reflective internal partitions, which mirror the waves back and forth until they reach the cavity.

Cooling Fan

To save you overheating of the microwave reactor, a cooling fan is integrated to use up excess heat.

Cavity

The cavity is a sealed steel structure that acts as an oscillator. within this hollow space, microwaves oscillate as standing waves, reflecting off the walls of the steel shape. this is facilitated by using the arrangement of two reflectors on both facet, which lets in the waves to superimpose, thereby growing their depth.

VIII. The Benefits of Employing Microwave Heating in Chemical Synthesis Can Be Summarized as Follows:

1. Step forward response charges.

2. Reduced reaction instances.

3. More advantageous chemical yields.

4. Uniform and selective heating

5. Milder reaction situations.

6. Reduced power consumption: Microwaves on the whole goal the sample, resulting in lower electricity utilization.

7. Fewer through merchandise, which results in higher purity and allows a more green work up and purification method.

8. Environmentally friendly and solvent-unfastened synthesis as compared to standard methods.

9. Simplified artificial techniques:  The microwave technique operates at accelerated temperatures, accelerating the reaction price.

10. Faster reactions: studies shows that microwave-assisted methods are extra sustainable than conventional procedures, substantially increasing reaction speed.

11. Decreased via-merchandise: This approach improves yields and purity, with aspirin synthesis attaining yields exceeding 80%.

IX. APPLICATIONS:

  1. Used for synthesis of pharmaceutical drugs (antibacterial, antifungal, anticancer agents)
  2. Helps in rapid drug discovery and development
  3. Applied in medicinal chemistry research for new bioactive compounds
  4. Used for preparation of benzimidazole, oxadiazole, imidazole derivatives
  5. Applied in green chemistry to reduce solvent use and pollution
  6. Used in industrial production of heterocyclic compounds
  7. Helps in synthesis of complex and fused heterocycles
  8. Applied in agrochemical synthesis (pesticides, herbicides, fungicides)
  9. Provides high yield and high purity of products
  10. Reduces reaction time from hours to minutes
  11. Saves energy and cost in chemical processes
  12. Produces fewer side products (high selectivity)
  13. Useful in academic and laboratory research work
  14. Applied in synthesis of bioactive natural product analogs

X. Synthesis:

1. Synthesis of Phenacetin:

Microwave-Assisted Reaction:  

Step I:  Dissolve 2 grams of p-amino phenol  in  6  milliliters  of  distilled  water  inside  a  conical  flask.  Introduce 2.2 milliliters of acetic anhydride even as  stirring  the  mixture.  Vigorously shake the reaction mixture and gently warmness it in a water bath tub till  a  nearly  clear  solution  is  acquired.  Subsequently, cool the conical flask in an ice tub.  Filter out the resulting product, wash it with cold water, and recrystallize it the use of hot water.

Step II:  In a round -bottom flask, vicinity 0.5 grams of easy sodium and add 10 milliliters of absolute alcohol. Once the energetic response has subsided, if  any  sodium remains  undisclosed,  warm  the  flask  in  a  water  bath  till  whole  dissolution  takes  place.  Allow the reaction mixture to chill, then include  three  grams  of  p-acetyl  amino  phenol.  Regularly add  four  grams  (2 milliliters)  of  ethyl  iodide  via  a  condenser.  Subject the combination to microwave irradiation  at  340  watts  for  five  mins.  In  a  while,  pour  in  20  milliliters  of  water  and  funky  the  round-bottom  flask  in  an  ice  tub.  Filter out the product and wash it with bloodless water.  If the answer reveals coloration, dissolve the crude product in 20 milliliters of rectified spirit. Upload 1 gram of activated charcoal and filter the combination. Treat the clear solution with hot water and  allow  it  to  chill.  Ultimately, filter out the usage of a pump and dry the product. Melting point: 132-134°C.

2. Synthesis Of P-Acetamidobenzenesulphonyl Chloride:

Microwave-Assisted Reaction:  In a 250ml spherical-bottom Erlenmeyer flask, regularly introduce 6 grams of dry powdered acetanilide into 14ml of chlorosulphonic acid even as every now and then shaking the aggregate. Subject the aggregate to microwave irradiation at 340 watts for 10 mins. After irradiation, permit the mixture to chill, and then carefully pour it over about 30 grams of beaten ice, resulting within the precipitation of sulphonyl chloride as a white stable. Filter out the sulphonyl chloride, wash it with water, and permit it to drain. Recrystallize the product the usage of chloroform. Melting factor: 147-149°C.

3. Synthesis of Benzoic Acid

Microwave-Assisted Reaction: In a 250 ml spherical backside flask, combine 3 grams of benzanilide with 10 ml of sulfuric acid. Subject the combination to microwave irradiation at 225 watts for 10 minutes. During this manner, a few benzoic acids will vaporize and sooner or later condense in the condenser. To facilitate the dislodging and partial dissolution of the benzoic acid, introduce 30 ml of hot water into the condenser. Later on, cool the flask in an ice-water bath, then clear out the mixture the usage of a Buchner funnel and allow it to dry. The melting factor of the product is one hundred twenty-122°C.

CONCLUSION:

Green Chemistry, imparting a sustainable and efficient opportunity to standard organic synthesis. By using microwave irradiation, this approach enhances response fees, improves yields, and minimizes byproduct formation even as decreasing the reliance on dangerous solvents. The mechanisms of microwave heating, together with dipolar polarization and ionic conduction, enable selective and uniform energy switch,  main  to  purifier  and greater chemical  methods. Comparative research verify the  advantages  of  MAOS  in  numerous  natural  reactions, highlighting its capacity for huge adoption in artificial chemistry. In spite of sure obstacles, such as protection concerns and solvent-unique absorption problems, MAOS is a promising  era  that  aligns  with  the  principles  of inexperienced  chemistry,  paving  the  manner  for  more  sustainable  and  strength green chemical  studies  and  industrial  applications.

REFERENCES

  1. M. A. Surati, S. Jauhari, K. R. Desai, A brief review: Microwave assisted organic reaction, Archives of Applied Science Research, (2012) 4(1): 645-661.
  2. Lidstrom P., Tierney J., Wathey B., Microwave assisted synthesis –a review, Tetrahedron 2001; 57: 9225-9283.
  3. S. Nain, R. Singh, S. Ravichandran, Importance of microwave heating in organic synthesis, Advanced Journal of Chemistry, (2019) 2(2): 94-104.
  4. A. S. Grewal, K. Kumar, S. Redhu, S. Bhardwaj, Microwave assisted synthesis: A Green chemistry approach, International Research Journal of Pharmaceutical and Applied Sciences, (2013) 3(5): 278-285.
  5. R. Gedye, F. Smith, S.Westaway, H. Ali, L. Baldisera, L. Laberge, J. Rousell, TetrahedronLett.27(1986)279.
  6. A. K. Nagariya, A. K. Meena, A. K. Yadav, U. S. Niranjan, A. K. Pathak, B. Singh, M. M. Rao, Microwave assisted organic reaction as new tool in organic synthesis, Journal of Pharmacy Research, (2010)3(3): 575-580
  7. Panwar N.L., Kaushik S.C., Kothari S. Renewable and Sustainable Energy Reviews, 2011, 15:1513 [Crossref], [Google Scholar], [Publisher];
  8. IbukunAduloju E., Yahaya N., Mohammad Zain N., Kamaruddin M.A., Abd Hamid M.A. Adv. J. Chem. A, 2023, 6:198 [Crossref], [Publisher];
  9. Wadje B.S., Bhosale V.N. Journal of Medicinal and Pharmaceutical Chemistry Research, 2023, 5:82 [Publisher];
  10. Ali F., Fazal S., Iqbal N., Zia A, Ahmad F. Journal of Medicinal and Nanomaterials Chemistry, 2023, 5:106 [Crossref], [Publisher];
  11. Li, C.-J.; Trost, B. M. Green chemistry for chemical synthesis. Proceedings of the National Academy of Sciences (PNAS), 2008, 105, 13197–13202.
  12. Driowya M., et al., Microwave-Assisted Synthesis of Bioactive Six-Membered Heterocycles and Their Fused Analogues, Molecules (2016).
  13. Microwave-Assisted Syntheses of Bioactive Seven-Membered, Macro-Sized Heterocycles and Their Fused Derivatives (review listing >100 references).
  14. Adhikari A., Bhakta S., Ghosh T., Microwave-Assisted Synthesis of Bioactive Heterocycles: An Overview, Tetrahedron (2022).
  15. Majhi S., Mondal K.P., Microwave-Assisted Synthesis of Heterocycles and Their Anti-Cancer Activities, Curr. Microwave Chem. (2023).
  16. Garella D., et al., Microwave-assisted synthesis of N-heterocycles in medicinal chemistry, MedChemComm (2013).
  17. Henary M., et al., Benefits and applications of microwave-assisted synthesis (green), RSC Advances (2020).
  18. Majumder A., Microwave-assisted synthesis of nitrogen-containing heterocycles, Org. Commun. (2013).
  19. Microwave-Assisted Organic Synthesis: An Eco-Friendly Method (intro review).
  20. Adhikari A.J., Devale R.P., Review on Microwave, The General Purpose in Microwave-Assisted Synthesis for Green Chemistry, Asian J. Res. Chem. (2022).
  21. Javahershenas R., Recent advances in microwave-assisted multicomponent reactions, RSC Advances (2024).
  22. Fan H., et al., Microwave assisted synthesis, antifungal activity of 1,2,4-triazolo[4,3-a] pyridines, BMC Chemistry (2016).
  23. Anwer K.E., et al., Green synthesis of heterocyclic pyrazole derivatives for cancer therapy, BMC Chemistry (2023).
  24. MDPI Proc. Synthesis of Bis-Heterocycles via Groebke-Blackburn-Bienaymé Reaction, MDPI (2024).
  25. Sauzem P.D., et al., Microwave-assisted synthesis of 5-trifluoromethyl pyrazoles (bioactive heterocycles).

Reference

  1. M. A. Surati, S. Jauhari, K. R. Desai, A brief review: Microwave assisted organic reaction, Archives of Applied Science Research, (2012) 4(1): 645-661.
  2. Lidstrom P., Tierney J., Wathey B., Microwave assisted synthesis –a review, Tetrahedron 2001; 57: 9225-9283.
  3. S. Nain, R. Singh, S. Ravichandran, Importance of microwave heating in organic synthesis, Advanced Journal of Chemistry, (2019) 2(2): 94-104.
  4. A. S. Grewal, K. Kumar, S. Redhu, S. Bhardwaj, Microwave assisted synthesis: A Green chemistry approach, International Research Journal of Pharmaceutical and Applied Sciences, (2013) 3(5): 278-285.
  5. R. Gedye, F. Smith, S.Westaway, H. Ali, L. Baldisera, L. Laberge, J. Rousell, TetrahedronLett.27(1986)279.
  6. A. K. Nagariya, A. K. Meena, A. K. Yadav, U. S. Niranjan, A. K. Pathak, B. Singh, M. M. Rao, Microwave assisted organic reaction as new tool in organic synthesis, Journal of Pharmacy Research, (2010)3(3): 575-580
  7. Panwar N.L., Kaushik S.C., Kothari S. Renewable and Sustainable Energy Reviews, 2011, 15:1513 [Crossref], [Google Scholar], [Publisher];
  8. IbukunAduloju E., Yahaya N., Mohammad Zain N., Kamaruddin M.A., Abd Hamid M.A. Adv. J. Chem. A, 2023, 6:198 [Crossref], [Publisher];
  9. Wadje B.S., Bhosale V.N. Journal of Medicinal and Pharmaceutical Chemistry Research, 2023, 5:82 [Publisher];
  10. Ali F., Fazal S., Iqbal N., Zia A, Ahmad F. Journal of Medicinal and Nanomaterials Chemistry, 2023, 5:106 [Crossref], [Publisher];
  11. Li, C.-J.; Trost, B. M. Green chemistry for chemical synthesis. Proceedings of the National Academy of Sciences (PNAS), 2008, 105, 13197–13202.
  12. Driowya M., et al., Microwave-Assisted Synthesis of Bioactive Six-Membered Heterocycles and Their Fused Analogues, Molecules (2016).
  13. Microwave-Assisted Syntheses of Bioactive Seven-Membered, Macro-Sized Heterocycles and Their Fused Derivatives (review listing >100 references).
  14. Adhikari A., Bhakta S., Ghosh T., Microwave-Assisted Synthesis of Bioactive Heterocycles: An Overview, Tetrahedron (2022).
  15. Majhi S., Mondal K.P., Microwave-Assisted Synthesis of Heterocycles and Their Anti-Cancer Activities, Curr. Microwave Chem. (2023).
  16. Garella D., et al., Microwave-assisted synthesis of N-heterocycles in medicinal chemistry, MedChemComm (2013).
  17. Henary M., et al., Benefits and applications of microwave-assisted synthesis (green), RSC Advances (2020).
  18. Majumder A., Microwave-assisted synthesis of nitrogen-containing heterocycles, Org. Commun. (2013).
  19. Microwave-Assisted Organic Synthesis: An Eco-Friendly Method (intro review).
  20. Adhikari A.J., Devale R.P., Review on Microwave, The General Purpose in Microwave-Assisted Synthesis for Green Chemistry, Asian J. Res. Chem. (2022).
  21. Javahershenas R., Recent advances in microwave-assisted multicomponent reactions, RSC Advances (2024).
  22. Fan H., et al., Microwave assisted synthesis, antifungal activity of 1,2,4-triazolo[4,3-a] pyridines, BMC Chemistry (2016).
  23. Anwer K.E., et al., Green synthesis of heterocyclic pyrazole derivatives for cancer therapy, BMC Chemistry (2023).
  24. MDPI Proc. Synthesis of Bis-Heterocycles via Groebke-Blackburn-Bienaymé Reaction, MDPI (2024).
  25. Sauzem P.D., et al., Microwave-assisted synthesis of 5-trifluoromethyl pyrazoles (bioactive heterocycles).

Photo
Nikita Pol
Corresponding author

Department of Pharmaceutical Chemistry Vidya Niketan College of Pharmacy, Lakhewadi, Indapur, Pune

Photo
Samrat Khedkar
Co-author

Department of Pharmaceutical Chemistry Vidya Niketan College of Pharmacy, Lakhewadi, Indapur, Pune

Photo
Mahesh Pingale
Co-author

Department of Pharmaceutical Chemistry Vidya Niketan College of Pharmacy, Lakhewadi, Indapur, Pune

Photo
Priyanka Chendke
Co-author

Department of Pharmaceutical Chemistry Vidya Niketan College of Pharmacy, Lakhewadi, Indapur, Pune

Photo
Om Walke
Co-author

Department of Pharmaceutical Chemistry Vidya Niketan College of Pharmacy, Lakhewadi, Indapur, Pune

Samrat Khedkar, Mahesh Pingale, Nikita Pol*, Priyanka Chendke, Om Walke, A Review on Microwave Assisted Green Synthesis of Bioactive Heterocycles, Int. J. Med. Pharm. Sci., 2026, 2 (7), 245-251. https://doi.org/10.5281/zenodo.21201523

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