ISSN

0974-4150 (Online)
0974-4169 (Print)


Author(s): Azam Z. Shaikh, Harsha Jadhav, Darshana M. Borse, Ritik. S. Jain

Email(s): ritikbadera390@gmail.com , azamph46@gmail.com , harsha.jadhav1345@gmail.com , darshanaborse84@gmail.com

DOI: 10.5958/0974-4150.2021.00028.6   

Address: Mr. Azam Z. Shaikh*, Mrs. Harsha Jadhav*, Ms. Darshana M. Borse, Mr. Ritik. S. Jain
Department of Pharmaceutical Chemistry, VEW `S Ahinsa Institute of Pharmacy, Dondaicha - 425408, Dist. Dhule, Maharastra India.
*Corresponding Author

Published In:   Volume - 14,      Issue - 2,     Year - 2021


ABSTRACT:
It is a branch of chemistry dealing with the synthesis, properties and applications of this heterocycles. Its play a very important role in nature and in chemical synthesis as well. Heterocyclic chemistry deals with heterocyclic compounds which constitute about sixty-five percent of organic chemistry literature. A heterocyclic compound or rings structure is a cyclic compound contain atom of at least two different elements as a member of its ring. In nature N, O, S, containing heterocyclic molecule can be found in every living being. A heterocyclic compound or ring structure is a cyclic compound that has atoms of at least two different elements as members of its ring(s). Examples of heterocyclic compounds include all of the nucleic acids, the majority of drugs, most biomass (cellulose and related materials), and many natural and synthetic dyes. More than half of known compounds are heterocycles. 59% of US FDA-approved drugs contain nitrogen heterocycles.


Cite this article:
Azam Z. Shaikh, Harsha Jadhav, Darshana M. Borse, Ritik. S. Jain. A Short Review on Structures and Synthesis of some Heterocyclic Compounds. Asian J. Research Chem. 2021; 14(2):149-151. doi: 10.5958/0974-4150.2021.00028.6

Cite(Electronic):
Azam Z. Shaikh, Harsha Jadhav, Darshana M. Borse, Ritik. S. Jain. A Short Review on Structures and Synthesis of some Heterocyclic Compounds. Asian J. Research Chem. 2021; 14(2):149-151. doi: 10.5958/0974-4150.2021.00028.6   Available on: https://ajrconline.org/AbstractView.aspx?PID=2021-14-2-11


REFERENCES:
1.    IUPAC Gold Book Heterocyclic compounds
2.    Jump up to: a b Thomas L. Gilchrist "Heterocyclic Chemistry" 3rd ed. Addison Wesley: Essex, England, 1997. 414 pp. ISBN 0-582-27843-0.
3.    Rees, Charles W. (1992). "Polysulfur-Nitrogen Heterocyclic Chemistry". Journal of Heterocyclic Chemistry. 29 (3): 639–651. DOI:10.1002/jhet.5570290306.
4.    Edon Vitaku, David T. Smith, Jon T. Njardarson (2014). "Analysis of The Structural Diversity, Substitution Patterns, and Frequency of Nitrogen Heterocycles among U.S. FDA Approved Pharmaceuticals". J. Med. Chem. 57: 10257-10274. DOI:10.1021/jm501100b. PMID 25255204.
5.    Kroehnke, Fritz (1976). "The Specific Synthesis of Pyridines and Oligopyridines". Synthesis. 1976 (1): 1–24. DOI:10.1055/s-1976-23941.
6.    Skell, P. S.; Sandler, R. S. (1958). "Reactions of 1,1-Dihalocyclopropanes with Electrophilic Reagents. Synthetic Route for Inserting a Carbon Atom Between the Atoms of a Double Bond". Journal of the American Chemical Society. 80 (8): 2024. DOI:10.1021/ja01541a070.
7.    Jones, R. L.; Rees, C. W. (1969). "Mechanism of heterocyclic ring expansions. Part III. Reaction of pyrroles with dichlorocarbene". Journal of the Chemical Society C: Organic (18): 2249. DOI:10.1039/J39690002249
8.    Gambacorta, A.; Nicoletti, R.; Cerrini, S.; Fedeli, W.; Gavuzzo, E. (1978). "Trapping and structure determination of an intermediate in the reaction between 2-methyl-5-t-butylpyrrole and dichlorocarbene". Tetrahedron Letters. 19 (27): 2439. DOI:10.1016/S0040-4039 (01)94795-1.
9.    Batsanov, A.; Howard, J.; Modal, R.; Steel, P. (2006). "The oxanorbornene approach to 3-hydroxy, 3,4-dihydroxy and 3,4,5-trihydroxy derivatives of 2-aminocyclohexanecarboxylic acid". Beilstein Journal of Organic Chemistry. 2 (9): 9. DOI:10.1186/1860-5397-29. PMC 1524792. PMID 16674802
10.    Katritzky, Alan R. (2003). "Synthesis of 2,4-disubstituted furans and 4,6-diaryl-substituted 2,3-benzo-1,3a,6a-triazapentalenes"2004 (2): 109. DOI:10.3998/ark.5550190.0005.208
11.    M. Tursky, L. L. R. Lorentz-Petersen, L. B. Olsen and R. Madsen, Org. Biomol. Chem., 2010, 8, 5576–5582
12.    https://pubs.rsc.org/en/content/articlehtml/2013/sc/c2sc21185h
13.    P. M. Jackson and C. J. Moody, J. Chem. Soc., Perkin Trans. 1, 1990, 2156–2158.
14.    P. G. Gassman, T. J. van Bergen and G. Gruetzmacher, J. Am. Chem. Soc., 1973, 95, 6508–6509.
15.    M. Tursky, L. L. R. Lorentz-Petersen, L. B. Olsen and R. Madsen, Org. Biomol. Chem., 2010, 8, 5576–5582.
16.    Hou, X. L.; Cheung, H. Y.; Hon, T. Y.; Kwan, P. L.; Lo, T. H.; Tong, S. Y.; Wong, H. N. (1998). "Regioselective syntheses of substituted furans". Tetrahedron. 54 (10): 1955–2020. DOI:10.1016/S0040-4020(97)10303-9.
17.    Katritzky, Alan R. (2003). "Synthesis of 2,4-disubstituted furans and 4,6-diaryl-substituted 2,3-benzo-1,3a,6a-triazapentalenes" (2004 (2): 109. DOI:10.3998/ark.5550190.0005.208
18.    Armarego, Wilfred L. F.; Chai, Christina L. L. (2003). Purification of Laboratory Chemicals (5th ed.). Elsevier. p. 346.
19.    Harreus, Albrecht Ludwig. "Pyrrole". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. DOI:10.1002/ 14356007.a22_453
20.    Lubell, W.; Saint-Cyr, D.; Dufour-Gallant, J.; Hopewell, R.; Boutard, N.; Kassem, T.; Dörr, A.; Zelli, R. (2013). "1H-Pyrroles (Update 2013)". Science of Synthesis. 2013 (1): 157–388.
21.    Walsh, Christopher T.; Garneau-Tsodikova, Sylvie; Howard-Jones, Annaleise R. (2006). "Biological formation of pyrroles: Nature's logic and enzymatic machinery". Natural Product Reports. 23 (4): 517. DOI:10.1039/b605245m
22.    Pyrrolidine, The Good Scents Company
23.    Bou Chedid, Roland; Melder, Johann-Peter; Dostalek, Roman; Pastre, Jörg; Tan, Aik Meam. "Process for the preparation of pyrrolidine". Google Patents. BASF SE. Retrieved 5 July 2019.

Recomonded Articles:

Author(s): Prathima Patil, S.P. Sethy, T. Sameena, K. Shailaja

DOI:         Access: Open Access Read More

Author(s): Ram C. Senwar, Krishna K. Rathore, Anita Mehta

DOI: 10.5958/0974-4150.2017.00022.0         Access: Open Access Read More

Author(s): Pankaj Baboo, Girendra Gautam, S.K. Gupta

DOI: 10.5958/0974-4150.2017.00039.6         Access: Open Access Read More

Author(s): KP Bhusari, ND Amnerkar, PB Khedekar, MK Kale, RP Bhole

DOI:         Access: Open Access Read More

Author(s): K. Kishore Kumar, R.S.K. Sharma, P. Chanti Babu, M. Sreenivasa Rao, K. Durga Prasadu, D. Ravi Kumar

DOI: 10.5958/0974-4150.2017.00067.0         Access: Open Access Read More

Author(s): Shashi Ravi Suman Rudrangi, Vijaya Kumar Bontha, Venkata Reddy Manda, Srinivas Bethi

DOI:         Access: Open Access Read More

Author(s): Gupta Akhilesh, Rawat Swati

DOI:         Access: Open Access Read More

Author(s): Subhasish Chaudhur, Biswajit Chandra Das

DOI:         Access: Open Access Read More

Author(s): Sunil Singh, Nitin Dubey, D.K. Jain

DOI:         Access: Open Access Read More

Author(s): Nikita N. Patel, Charmy S. Kothari

DOI:         Access: Open Access Read More

Author(s): Saurabh Chaturvedi, Rakesh Saini, AN Kesari, Awani Rai, Neelotma Maurya, M ShaharYar

DOI:         Access: Open Access Read More

Author(s): Firke SD, Firake BM, Chaudhari RY, Patil VR

DOI:         Access: Open Access Read More

Author(s): Pandeya S. N., Neha Rajput

DOI:         Access: Open Access Read More

Asian Journal of Research in Chemistry (AJRC) is an international, peer-reviewed journal devoted to pure and applied chemistry..... Read more >>>

RNI: Not Available                     
DOI: 10.5958/0974-4150 

Popular Articles


Recent Articles




Tags