Figure and Facts

Google Scholar h-index

4

Google Scholar i10-index

00

Google Scholar Citation

36

WOS Citation

43

h-index (Web of Science)

5

Average citations per item

2.7

Issue per year

4

No. of volumes

1

No. of Issues

4

Number of Articles

20

Number of Submissions

41

Rejected Submissions

11

Acceptance rate

49

Accept Date (Days)

         36

Review papers

 0

No. of contributors

61

Article view

4,013

View Per Article

200.65

PDF download

2,871

PDF Download Per Article

143.55

No. of reviewers

87

Contributing countries

3

No. of databases

11

Journal of Applied Organometallic Chemistry                         

J. Appl. Organomet. Chem.

DOI: 10.22034/JAOC

Journal of Applied Organometallic Chemistry (JAOC) was launched by Sami Publishing Company in 2021. This double peer-reviewed and indexed journal aim to provide a platform for researchers around the world to share their latest findings in all field of Chemistry. Experimental, theoretical and applied original research studies in all fields of chemistry are welcomed for submission. The journal is Open Access with article processing charges and all articles published in this journal are freely available for readers online at http://jaoc.samipubco.com without a subscription and authors retain the copyright of their work.

JAOC is published Quarterly (online and in print= 4 Issues per year).

The average time between submission and final decision is eight weeks and the average time between acceptance and publication is six weeks.

The JAOC Journal has been indexed in the well-known world databases (You can check the related Link). All submitted manuscripts are checked for similarity through a trustworthy software named iThenticate to be assured about its originality and then rigorously peer-reviewed by the international reviewers.

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Original Article
A novel approach for total synthesis of Stemona alkaloid: Tuberostemonamide
1. A novel approach for total synthesis of Stemona alkaloid: Tuberostemonamide

Mir Monir Hossain; Tasmuna Tamrin Tanmy

Volume 1, Issue 4 , Autumn 2021, Pages 159-164

http://dx.doi.org/10.22034/jaoc.2021.304913.1037

Abstract
  Stemona alkaloids, are structurally complex and polycyclic alkaloids, obtained from a novel class of natural plants which are extracted, separated, and purified from Stemonaceae family. ...  Read More
Original Article
Green synthesis, characterization and biological activity of aryl Azo Schiff bases
2. Green synthesis, characterization and biological activity of aryl Azo Schiff bases

Ravindra S shinde; Nanda S. Korde; Rahul A More

Volume 1, Issue 4 , Autumn 2021, Pages 165-173

http://dx.doi.org/10.22034/jaoc.2021.292290.1026

Abstract
  We report a novel and eco-friendly methods approving the green synthesis of various Schiff’s bases by sonication, microwave irradiation, stirring and grinding methods using DHE ...  Read More
Iodine‐DMSO Catalyzed aromatization of Polysubstituted Cyclohexanone derivatives; An efficient methods for the synthesis of polyfunctionized Biaryls derivatives
1. Iodine‐DMSO Catalyzed aromatization of Polysubstituted Cyclohexanone derivatives; An efficient methods for the synthesis of polyfunctionized Biaryls derivatives

Sunil V. Gaikwad; Milind V. Gaikwad; Pradeep D. Lokhande

Volume 1, Issue 1 , Winter 2021, , Pages 1-8

http://dx.doi.org/10.22034/jaoc.2021.128538

Abstract
  AbstractWe have developed a simple method for the regioselective aromatization of Polysubstituted Cyclohexanone derivatives in the presence of iodine (25 mol %), Pd/C (10Mol%) in dimethyl ...  Read More
Computational Chemistry Approach for the Investigation of Structural, Electronic, Chemical and Quantum Chemical Facets of Twelve Biginelli Adducts
2. Computational Chemistry Approach for the Investigation of Structural, Electronic, Chemical and Quantum Chemical Facets of Twelve Biginelli Adducts

Vishnu A Adole

Volume 1, Issue 1 , Winter 2021, , Pages 29-40

http://dx.doi.org/10.22034/jaoc.2021.278598.1009

Abstract
  The rising concerns about the Biginelli reaction are mainly attributable to the therapeutic and pharmacological features of Biginelli adducts, especially dihydropyrimidinones (DHPMs). ...  Read More
Anti-microbial evaluation, Experimental and Theoretical Insights into Molecular Structure, Electronic Properties, and Chemical Reactivity of (E)-2-((1H-indol-3-yl)methylene)-2,3-dihydro-1H-inden-1-one
3. Anti-microbial evaluation, Experimental and Theoretical Insights into Molecular Structure, Electronic Properties, and Chemical Reactivity of (E)-2-((1H-indol-3-yl)methylene)-2,3-dihydro-1H-inden-1-one

Rahul Shinde; Vishnu A Adole

Volume 1, Issue 2 , Spring 2021, , Pages 48-58

http://dx.doi.org/10.22034/jaoc.2021.278742.1011

Abstract
  The present investigation describes antimicrobial, computational, study of (E)-2-((1H-indol-3-yl)methylene)-2,3-dihydro-1H-inden-1-one (IMDHI) molecule. The spectroscopic characterization ...  Read More
Synthesis, Spectral and Biological Studies of DHA Schiff Bases
4. Synthesis, Spectral and Biological Studies of DHA Schiff Bases

Shubham Bhagwatrao Biradar; Dnyaneshwar Vithal Narte; Rushikesh Pradip Kale; Kalimoddin Inayatsab Momin; Maroti Sayabu Sudewad; Kundan Chandramani Tayade; Dhananjay Gangadhar Palke

Volume 1, Issue 1 , Winter 2021, , Pages 41-47

http://dx.doi.org/10.22034/jaoc.2021.275758.1003

Abstract
  ABSTRACTA new series of Schiff bases derived from DHA (Dehydroacetic acid) and aromatic primary amines were synthesized and characterized by elemental and spectral (Electronic, IR and ...  Read More
Regioselective One-pot transformation of 2’-hydroxy chalcones to 3,5-diphenylisoxazole via dehydrogenation of dihydroisoxazolines using Copper salt in DMF
5. Regioselective One-pot transformation of 2’-hydroxy chalcones to 3,5-diphenylisoxazole via dehydrogenation of dihydroisoxazolines using Copper salt in DMF

Milind V Gaikwad

Volume 1, Issue 2 , Spring 2021, , Pages 59-65

http://dx.doi.org/10.22034/jaoc.2021.278705.1010

Abstract
  A synthesis of series of 3, 5-diaryl isoxazoles has been described. The Cu salt in DMF with EDU base induces oxidative dehydrogenation of 2-(5-phenyl-4,5-dihydroisoxazol-3-yl) phenol ...  Read More

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