An Overview of Retrosynthetic Methods, Evaluation, and Mechanism

Authors

  • Dudekula Khasimvali Priyadarshini Institute of pharmaceutical Education and Research, 5th Mile, Pulladigunta, Guntur -522017, Andhra Pradesh, India.

Keywords:

Retrosynthesis, Synthon, FGI, Bond Disconnection

Abstract

One particular area of chemical synthesis in organic chemistry is called organic synthesis. Chemical synthesis is a highly effective tool for humans because it yields a wide range of valuable compounds, particularly those that are either entirely absent from or present in very little amounts in nature. In organic chemistry, the concept of retrosynthesis examines the possibility of creating a complex organic molecule through the process of reverse synthesis. Retrosynthesis is an essential process for creating complicated molecules by going in the other direction—that is, breaking bonds. Rules must be followed by many principles. In order to overcome the difficulties posed by various reaction processes, concepts, and factors in organic synthesis, total synthesis, and asymmetric synthesis, "retrosynthesis" is a crucial strategy. Its synthetic routes are also simpler and easier to develop and construct. Because organic synthesis is influenced by a multitude of reaction mechanisms, concepts, and factors, "retrosynthesis" is a crucial technique for resolving its synthetic routes. It is less complex and easier to design and conceptualize than organic synthesis, total synthesis, and asymmetric synthesis.

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References

E. J. Corey, X-M (1995), Cheng, Basics of Retrosynthetic Analysis: A Review for Beginners, Dean&Francis, pg.no 1-8. https://www.deanfrancispress.com/articles/all/IC1227.pdf

Carey F.A. The brief introduction and extension to Retrosynthesis, Dean&Francis, pg.no 1-8.

Clayden, Jonathan, Introduction to Retrosynthesis: Strategies and Approaches Organic Chemistry, Web of Conferences, pg.no 1-8.

https://iroch.ir/wp-content/uploads/2020/12/Clayden-Organic-Chemistry-2nd-edition- c2012-txtbk.pdf

Ashenhurst, J. (2022, August 17). Retrosynthesis-Introduction to the Analysis and Mechanism, The 3rd International Conference on Materials Chemistry and Environmental Engineering, pg.no- 143-160

Liu, Luhao & Zheng, Jiaying. (2023). Retrosynthesis-Introduction to the Analysis and Mechanism. Applied and Computational Engineering. 3. 143-160. 10.54254/2755-2721/3/20230391.

Hwisa, Nagiat Tayeb; Katakam, Prakash; Chandu, Babu Rao; Ismael, Mraa Hazim; Bader, Abdalwahab; Pandemic influenza A (H1N1) vaccination among libyan health care personnel: A cross-sectional retrospective study Journal of Pharmacy and Bioallied sciences 6 3 192-197 2014

Peraman, Ramalingam & Ganapaty, S & Baburao, C & Ravi, TK. (2006). Impact of 4-thiazolidinones and 2-azetidinones on antimicrobial spectrum of nalidixic acid. ACTA CIENCIA INDICA CHEMISTRY. 32. 433.

II S. M. Sc. Chemistry (SEM I & II) Syllabus (80 Credit course) as per NEP 2020 for AY 2022-23 SEM I.

Assaleh FH, Katakam P, Botcha R, Chandu BR, Adiki SK. Synthesis and characterisation of starch tartrate and its application as novel disintegrant in telmisartan tablets. Starch‐Stärke. 2014 Mar;66(3-4):409-17.

Akhter, J. (2022, September Retrosynthesis-Introduction to the Analysis and Mechanism, The 3rd International Conference on Materials Chemistry and Environmental Engineering, pg.no- 143-160

Ramalingam P, Baburao C, Ganapaty S. Synthesis of some'N'bridgehead heterocycles containing quinoxaline and 1, 2, 4-triazole and their antifungal and antitubercular activity. Asian Journal of Chemistry. 2008 Jul 1;20(5):4132.

Ramalingam P, Baburao C, Ganapaty S. Synthesis of some'N'bridgehead heterocycles containing quinoxaline and 1, 2, 4-triazole and their antifungal and antitubercular activity. Asian Journal of Chemistry. 2008 Jul 1;20(5):4132.

Namballa M, Adimulapu A, Jesudasan RE. QbD Assisted Optimization of Microwave-assisted Synthesis of Polyacrylamide Grafted Tragacanth: Characterization and Instrumental Analysis. Current Microwave Chemistry. 2024 Apr 1;11(1):16-29.

Ramalingam P, Ganapaty S, Rao CB, Ravi TK. Synthesis of some new coumarino [4, 3-b] pyrido [6, 5-c] cinnolines as potent antitubercular agents. Indian Journal of Heterocyclic Chemistry. 2006 Apr 1;15(4):359-62.

Wang J, Ji Y, Tian Y, Fang T. Basics of Retrosynthetic Analysis: A Review for Beginners.

https://www.deanfrancispress.com/articles/all/IC1227.pdf

Warren, S. (n.d.). A Programmed Introduction to the Synthon Approach Designing Organic Syntheses, pg.no 205-304.

COREY, E. J. (1967). The brief introduction and extension to Retrosynthesis, Dean&Francis, pg.no 1-8.

Koca J, Kratochvil M, Kvasnicka V, Matyska L, Pospichal J. Synthon model of organic chemistry and synthesis design. Springer Science & Business Media; 2012 Dec 6. https://chem.yonsei.ac.kr/chem/upload/CHE6402-01/119004404248922.pdf

Corey EJ, Wipke WT. Computer-Assisted Design of Complex Organic Syntheses: Pathways for molecular synthesis can be devised with a computer and equipment for graphical communication. Science. 1969 Oct 10;166(3902):178-92.

Mikolajczyk A, Zhdan U, Antoniotti S, Smolinski A, Jagiełło K, Skurski P, Harb M, Puzyn T, Polanski J. Retrosynthesis from transforms to predictive sustainable chemistry and nanotechnology: a brief tutorial review. Green Chemistry. 2023.

Bharati V Badami, Art of Planning Organic Synthesis, pg.no 1071–1086.

Liu X, Liu J, Wu J, Li CC. Enantioselective Total Synthesis of Cerorubenic Acid-III via Type II [5+ 2] Cycloaddition Reaction. The Journal of Organic Chemistry. 2021 Apr 22;86(16):11125-39.

Published

28-07-2024

How to Cite

Dudekula, K. (2024). An Overview of Retrosynthetic Methods, Evaluation, and Mechanism. International Journal of Current Innovations in Advanced Research, 7(2), 52–63. Retrieved from https://www.ijciar.com/index.php/journal/article/view/177

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Section

Review Articles