Design of Synthetic Strategies towards Sulfur Containing Scaffolds

Sambasivarao Kotha; Priti Khedkar

doi:10.1055/s-0043-1775393

Synthesis, Inhaltsverzeichnis

Synthesis 2025; 57(02): 275-295
DOI: 10.1055/s-0043-1775393

review

Special Topic Dedicated to Prof. H. Ila

Design of Synthetic Strategies towards Sulfur Containing Scaffolds

Sambasivarao Kotha∗

^aDepartment of Chemistry, Sunandan Divatia School of Science, SVKM’s NMIMS (Deemed-to-Be) University, Vile Parle (W), Mumbai, Maharashtra 400056, India

,

Priti Khedkar

^bDepartment of Chemistry, Guru Nanak Khalsa College of Arts, Science and Commerce (Autonomous), Matunga, Mumbai, Maharashtra, 400019, India

› Institutsangaben

Abstract

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Abstract

The utilization of sulfur heterocycles in organic synthesis has attracted significant attention due to their wide-ranging applications. This review showcases the syntheses of diverse sulfur heterocycles embedded with amino acid derivatives, polycycles, spirocycles, cyclophanes, and other complex scaffolds. The reported methods extend beyond compound synthesis and highlight the use of different sulfur reagents for constructing sulfur heterocycles. This Review also discusses the utility of a variety of sulfur-containing starting materials for the generation of complex target molecules.

1 Introduction

2 Potassium Thioacetate

3 Thiazolidine-2,4-dione

4 Rhodanines

5 Sodium Sulfide

6 Thiotetronic Acid

7 Thiadiazoles

8 Thiophene

9 Rongalite

10 Sulfur Dioxide

11 Divinyl Sulfone

12 Sulfur Heterocycles Based on Boronic Acids

13 Miscellaneous

14 Summary

Key words

sulfur heterocycles - potassium thioacetate - thiazolidine-2,4-dione - rhodanines - thiotetronic acid - thiadiazole - thiophene - rongalite

Volltext

Referenzen

References

1a Sulfur Chemistry. In Topics in Current Chemistry. Jiang X. Springer; Cham: 2019
1b Bambas LL. Five-Membered Heterocyclic Compounds with Nitrogen and Sulfur or Nitrogen, Sulfur, and Oxygen (Except Thiazole), Vol. 4. Weissberger A. John Wiley & Sons; New York: 2008
1c Breslow DS, Skolnik H. Multi-Sulfur and Sulfur and Oxygen Five- and Six-Membered Heterocycles. In The Chemistry of Heterocyclic Compounds, Part 1, Vol. 21. Weissberger A. John Wiley & Sons; New York: 2008

2a Pathania S, Narang RK, Rawal RK. Eur. J. Med. Chem. 2019; 180: 486
2b Ferro CT. B, dos Santos BF, da Silva CD. G, Brand G, da Silva BA. L, Domingues NL. C. Curr. Org. Synth. 2020; 17: 192

3 Kaloni TP, Giesbrecht PK, Schreckenbach G, Freund MS. Chem. Mater. 2017; 29: 10248

4a Groenendaal L, Zotti G, Aubert P.-H, Waybright SM, Reynolds JR. Adv. Mater. 2003; 15: 855
4b Heywang G, Jonas F. Adv. Mater. 1992; 4: 116
4c Kirchmeyer S, Reuter K. J. Mater. Chem. 2005; 15: 2077

5a Cohen SM, Fukushima S, Gooderham NJ, Guengerich FP, Hecht SS, Rietjens IM. C. M, Smith RL, Bastaki M, Harman CL, McGowen MM, Valerio LG. Jr, Taylor SV. Food Chem. Toxicol. 2017; 99: 40
5b Maga JA, Katz I. C R C Crit. Rev. Food Sci. Nutr. 1975; 6: 153

6 Devendar P, Yang G.-F. Sulfur-Containing Agrochemicals. In Sulfur Chemistry, Chap. 2. Jiang X. Topics in Current Chemistry Collections; Springer; Cham: 2019
7 Murphree SS. Heterocyclic Dyes: Preparation, Properties, and Applications. In Progress in Heterocyclic Chemistry, Vol. 22. Gribble G, Joule JA. Elsevier; Oxford: 2011: 21-58
8 Steingruber E. Indigo and Indigo Colorants. In Ullmann’s Encyclopedia of Industrial Chemistry. Wiley-VCH; Weinheim: 2004
9 Khan I, Saeed K, Zekker I, Zhang B, Hendi AH, Ahmad A, Ahmad S, Zada N, Ahmad H, Shah LA, Shah T, Khan I. Water 2022; 14: 242
10 Qiao Z, Jiang X. Potassium Thioacetate. In e-EROS Encyclopedia of Reagents for Organic Synthesis. John Wiley & Sons; Chichester: 2014
11 Soria-Castro SM. Synlett 2012; 23: 2997

12a Ogaba OM, Warner NC, O’Leary DJ, Grubbs RH. Chem. Soc. Rev. 2018; 47: 4510
12b Yu M, Lou S, Gonzalez-Bobes F. Org. Process Res. Dev. 2018; 22: 918
12c Groso EJ, Schindler CS. Synthesis 2019; 51: 1100
12d Alkene Metathesis in Organic Synthesis. In Topics in Organometallic Chemistry. Fürstner A. Springer-Verlag; Berlin: 1988
12e Ivin KJ, Mol JC. Olefin Metathesis and Metathesis Polymerization. Academic Press; San Diego: 1997

For our reviews, see:

12f Kotha S, Mesharam M. Chem. Asian J. 2018; 13: 1758
12g Kotha S, Dipak MK. Tetrahedron 2012; 68: 397
12h Kotha S, Lahiri K. Synlett 2007; 2767
12i Kotha S, Sreenivasachary N. Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 2001; 40: 763

13 Kotha S, Gupta N, Ansari S. Eur. J. Org. Chem. 2020; 6929
14 Kotha S, Ansari S, Gupta N. IUCr Data 2020; 5: x201464
15 Kotha S, Gupta NK, Solanke BU. ChemistrySelect 2023; 8: e202302672
16 Kotha S, Gupta NK, Ansari S. Asian J. Org. Chem. 2023; 12: e202200649
17 Kotha S, Gaikwad V, Chourasia UV. Asian J. Org. Chem. 2022; 11: e202200598

18a Visentini P. Farmaco, Ed. Sci. 1954; 9: 274
18b Rekha S, Shantharam U, Chandy V. Int. Res. J. Pharm. 2011; 2: 81
18c Youssef AM, White MS, Villanueva EB, El-Ashmawy IM, Klegeris A. Bioorg. Med. Chem. 2010; 18: 2019
18d Shimazaki N, Togashi N, Hanai M, Isoyama T, Wada K, Fujita T, Fujiwara K, Kurakata S. Eur. J. Cancer 2008; 44: 1734
18e Subtel’na I, Atamanyuk D, Szymańska E, Kieć-Kononowicz K, Zimenkovsky B, Vasylenko O, Gzella A, Lesyk R. Bioorg. Med. Chem. 2010; 18: 5090

19a Sohda T, Mizuno K, Tawada H, Sugiyama Y, Fujita T, Kawamatsu Y. Chem. Pharm. Bull. 1982; 30: 3563
19b Lehmann JM, Moore LB, Smith-Oliver TA, Wilkison WO, Willson TM, Kliewer SA. J. Biol. Chem. 1995; 270: 12953

20a Kotha S, Panguluri NR, Ali R. Eur. J. Org. Chem. 2017; 5316
20b Wang Q, Liu H.-F, Ren S.-Y, He M.-X, Pan Y.-M. Synthesis 2023; 55: 2873

21a Matton P, Huvelle S, Haddad M, Phansavath P, Ratovelomanana-Vidal V. Synthesis 2022; 54: 4
21b Shibata Y, Tanaka K. Synthesis 2012; 44: 323
21c Domínguez G, Pérez-Castells J. Chem. Soc. Rev. 2011; 40: 3430
21d Kotha S, Lahiri K, Sreevani G. Synlett 2018; 29: 2342
21e Kotha S, Brahmachary E, Lahiri K. Eur. J. Org. Chem. 2005; 4741

22 Kotha S, Sreevani G, Dzhemileva LU, Yunusbaeva MM, Dzhemilev UM, D’yakonov VA. Beilstein J. Org. Chem. 2019; 15: 2774
23 Kotha S, Gaikwad V. J. Chem. Sci. 2022; 134: 58
24 Brosge F, Singh P, Almqvist F, Bolm C. Org. Biomol. Chem. 2021; 19: 5014
25 Ziarani GM, Ebrahimi D, Mohajer F, Varma RS, Iravani S. ChemistrySelect 2023; 8: e202302152
26 Kotha S, Gaikwad V. Heterocycles 2022; 104: 541

27a Tomasic T, Masic LP. Curr. Med. Chem. 2009; 16: 1596
27b Chaurasyia A, Chawla P, Monga V, Singh G. Chem. Biol. Drug Des. 2023; 101: 500

28 Kotha S, Sreevani G. Eur. J. Org. Chem. 2018; 5935
29 Ma F.-P. Synlett 2011; 18: 2759
30 Kotha S, Gunta R. Beilstein J. Org. Chem. 2015; 11: 1373
31 Kotha S, Gunta R. Heterocycles 2019; 98: 271
32 Sakya SM, Suarez-Contreras M, Dirlam JP, O’Connell TN, Hayashi SF, Santoro SL, Kamicker BJ, George DM, Ziegler CB. Bioorg. Med. Chem. Lett. 2001; 11: 2751
33 Kotha S, Deb A. Ind. J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 2008; 47: 1120
34 Kotha S, Mandal K, Deb AC, Banerjee S. Tetrahedron Lett. 2004; 45: 9603

35a Jain AK, Sharma S, Vaidya A, Ravichandran V, Agrawal RK. Chem. Biol. Drug Des. 2013; 81: 557
35b Hu Y, Li C.-Y, Wang X.-M, Yang Y.-H, Zhu H.-L. Chem. Rev. 2014; 114: 5572

36a Tahghighi A, Babalouei F. Iran. J. Basic Med. Sci. 2017; 20: 613
36b Li Y, Geng J, Liu Y, Yu S, Zhao G. ChemMedChem 2013; 8: 27
36c Haider S, Alam MS, Hamid H. Eur. J. Med. Chem. 2015; 92: 156

37 Kotha S, Singh D. J. Mol. Struct. 2023; 1275: 134600

38a Abedinifar F, Babazadeh Rezaei E, Biglar M. Mol. Diversity 2021; 25: 2571
38b Shah R, Verma PK. Chem. Cent. J. 2018; 12: 137

39 Kotha S, Kashinath D, Lahiri K, Sunoj RB. Eur. J. Org. Chem. 2004; 4003
40 Kotha S, Todeti S, Gopal MB, Datta A. ACS Omega 2017; 2: 6291
41 Kotha S, Chinnam AK, Shirbhate ME. Beilstein J. Org. Chem. 2015; 11: 1514

42a Kotha S, Behera M, Kumar RV. Bioorg. Med. Chem. Lett. 2002; 12: 105
42b Kotha S, Behera M. J. Pept. Res. 2004; 64: 72

43 Damodharan L, Pattabhi V, Behera M, Kotha S. J. Mol. Struct. 2004; 705: 101
44 Kotha S, Behera M, Shah VA. Synlett 2005; 12: 1877

45a Makarov SV, Horváth AK, Silaghi-Dumitrescu RJ, Gao Q. Sodium Dithionite, Rongalite and Thiourea Oxides: Chemistry and Application. World Scientific Publishing; London: 2016
45b Makarov SV, Silaghi-Dumitrescu R. J. Sulfur Chem. 2013; 34: 444

46a Kotha S, Khedkar P. Chem. Rev. 2012; 112: 1650
46b Chen J.-X. Synlett 2012; 23: 157
46c Kotha S, Kheadkar P, Dommaraju Y. Tetrahedron Lett. 2019; 60: 631
46d Ali R. ChemistrySelect 2023; 8: e202302903

47a Kotha S, Krishna NG. Curr. Sci. 2011; 101: 923
47b Kotha S, Meshram M. Synthesis 2014; 46: 1525

48 Kotha S, Ganesh T, Ghosh AK. Bioorg. Med. Chem. Lett. 2000; 10: 1755
49 Kotha S, Deodhar D, Khedkar P. Org. Biomol. Chem. 2014; 12: 9054
50 Kotha S, Banerjee S. Synthesis 2007; 1015

51a Kotha S, Bansal D, Chavan AS. ACS Omega 2019; 4: 22261
51b Kotha S, Chavan AS, Goyal D. ACS Comb. Sci. 2015; 17: 253
51c Kotha S, Meshram M, Tiwari A. Chem. Soc. Rev. 2009; 38: 2065

52 Kotha S, Ghosh AK. Tetrahedron Lett. 2004; 45: 2931
53 Kotha S, Ghosh AK. Tetrahedron 2004; 60: 10833
54 Ghosh AK. Ph.D. Thesis. Indian Institute of Technology-Bombay; India: 2004
55 Kotha S, Kumar Gupta N, Sreevani G, Rao Panguluri N. Chem. Asian J. 2021; 16: 3649
56 Kotha S, Meshram M. Heterocycles 2015; 90: 357
57 Kotha S, Ghosh A. Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 2006; 45: 227
58 Kotha S, Mishram M. Heterocycles 2011; 82: 1663
59 Kotha S, Misra S, Srinivas V. Eur. J. Org. Chem. 2012; 4052

60a Kotha S, Ali R. Tetrahedron 2015; 71: 6944
60b Kotha S, Ali R. Heterocycles 2014; 88: 789

61 Kotha S, Ali R. Tetrahedron 2015; 71: 1597
62 Kotha S, Ali R. Tetrahedron Lett. 2015; 56: 2172
63 Kotha S, Ali R. Tetrahedron Lett. 2015; 56: 3992
64 Sreevani G. Ph.D. Thesis. Indian Institute of Technology-Bombay; India: 2018
65 Kotha S, Sreevani G. Synthesis 2018; 50: 4883

66a Fetzer JohnC, Winefordner JamesD. The Chemistry and Analysis of the Large Polycyclic Aromatic Hydrocarbons. John Wiley & Sons; New York: 2000
66b Goyal H, Kumar P, Gupta R. Chem. Asian J. 2023; 18: e202300355

67 Kotha S, Aswar VR, Manchoju A. Tetrahedron 2016; 72: 2306

68a Mandal B, Karmakar I, Brahmachari G. Chem. Biodivers. 2022; 19: e202200484
68b Krawczyk H. Int. J. Mol. Sci. 2023; 24: 12066

69 Kotha S, Ali R. Heterocycles 2015; 99: 645
70 Kotha S, Khedkar P. J. Org. Chem. 2009; 74: 5667
71 Kotha S, Sreevani G. Heterocycles 2017; 95: 1204
72 Kotha S, Chavan A. J. Org. Chem. 2010; 75: 4319
73 Kotha S, Sreevani G. ChemistrySelect 2017; 2: 10804
74 Kotha S, Khedkar P, Ghosh AK. Eur. J. Org. Chem. 2005; 3581
75 Kotha S, Kashinath D, Khedkar P. Synthesis 2007; 3357

76a Burke SD. In Encyclopedia of Reagents for Organic Synthesis. Paquette LA. John Wiley & Sons; Chichester: 2001
76b Pelzer G, Herwig J, Keim W, Goddard R. Russ. Chem. Bull. 1998; 47: 904
76c Hoffman RV. Org. Synth. 1981; 60: 121
76d Malet-Sanz L, Madrzak J, Ley SV, Baxendale IR. Org. Biomol. Chem. 2010; 8: 5324

77 Vogel P, Turks M, Bouchez L, Markovic D, Varela-Álvarez A, Sordo J. Á. Acc. Chem. Res. 2007; 40: 931

78a Whitham GH. Organosulfur Chemistry. Oxford University Press; Oxford/New York: 1995
78b Organic Chemistry of Sulfur. Oae S. Plenum Press; New York: 1977
78c Stirling CJ. M. Organic Sulphur Chemistry: Structure, Mechanism, and Synthesis. Butterworths; London/Boston: 1975
78d The Chemistry of Sulphones and Sulphoxides. In Patai’s Chemistry of Functional Groups. Patai S, Rappoport Z, Stirling CJ. M. Wiley-Blackwell; New York: 1988

79 Kotha S, Vijayalakshmi B. Heterocycles 2015; 90: 226

80a Morales-Sanfrutos J, Lopez-Jaramillo FJ, Elremaily MA. A, Hernández-Mateo F, Santoyo-Gonzalez F. Molecules 2015; 20: 3565
80b Santos J, Rueda N, Barbosa O, Fernández-Sánchez J, Medina-Castillo A, Ramon-Marquez T, Arias-Martos M, Millán-Linares M, Pedroche J, Yust M, Gonçalves L, Fernández-Lafuente R. RSC Adv. 2015; 5: 20639

81 Bieniek M, Kołoda D, Grela K. Org. Lett. 2006; 8: 5689
82 Teyssot M, Fayolle M, Philouze C, Dupuy C. Eur. J. Org. Chem. 2003; 54

83a Kotha S, Meshram M, Aswar VR. Chem. Asian J. 2023; 18: e202300355
83b Kotha S, Meshram M, Khedkar P, Banerjee S, Deodhar D. Beilstein J. Org. Chem. 2015; 11: 1833
83c Holub N, Blechert S. Chem. Asian J. 2007; 2: 1064

84 Kotha S, Fatma A. ChemistrySelect 2020; 5: 1929
85 de Jesus Hiller N, do Amaral e Silva NA, Tavares TA, Faria RX, Eberlin MN, de Luna Martins D. Eur. J. Org. Chem. 2020; 4841

86a Farhang M, Akbarzadeh AR, Rabbani M, Ghadiri AM. Polyhedron 2022; 227: 116124
86b Hooshmand SE, Heidari B, Sedghi R, Varma RS. Green Chem. 2019; 21: 381
86c Kotha S, Meshram M. Beilstein J. Org. Chem. 2018; 14: 2468
86d Maluenda I, Navarro O. Molecules 2015; 20: 7528
86e Kotha S, Mandal K. Chem. Asian. J. 2009; 4: 354
86f Kotha S, Lahiri K. Eur. J. Org. Chem. 2007; 1221
86g Kotha S, Lahiri K, Kashinath D. Tetrahedron 2002; 58: 9633

87a António JP. M, Russo R, Carvalho CP, Cal PM. S. D, Gois PM. P. Chem. Soc. Rev. 2019; 48: 3513
87b Hall DG. Chem. Soc. Rev. 2019; 48: 3475
87c Silva MP, Saraiva L, Pinto M, Sousa ME. Molecules 2020; 25: 4323

88a Alshubramy MA, Alamry KA, Hussein MA. RSC Adv. 2023; 13: 14317
88b Antonijevic M, Rochais C, Dallemagne P. Molecules 2023; 28: 679
88c Kotha S, Meshram M, Punguluri NR, Shah V, Saidulu T, Shirbhate M. Chem. Asian J. 2019; 14: 1356

89 Kotha S, Chakraborty K, Brahmachary E. Synlett 1999; 1621
90 Thallapally PK, Chakraborty K, Carrell HL, Kotha S, Desiraju GR. Tetrahedron 2000; 56: 6721
91 Kotha S, Ghosh AK, Deodhar KD. Synthesis 2004; 549
92 Kotha S, Ghosh AK. Synlett 2002; 451
93 Kotha S, Lahiri K, Sreenivasachary N. Synthesis 2001; 1932

94a Ma J, Yan L, Yang J, He Y, Wu L. ChemBioChem 2024; 25: e202300481
94b Brytan W, Padrela L. J. Drug Delivery Sci. Technol. 2023; 89: 104992
94c Boto A, González CC, Hernández D, Romero-Estudillo I, Saavedra CJ. Org. Chem. Front. 2021; 8: 6720
94d Hou H, Wang J, Wang J, Tang W, Shaikh AS, Li Y, Fu J, Lu L, Wang F, Sun F, Tan H. J. Biomed. Nanotechnol. 2020; 16: 1687
94e Kotha S, Mesharam M, Rao PN. Synthesis 2019; 51: 1913
94f Kotha S, Lahiri K. Curr. Med. Chem. 2005; 12: 849
94g Kotha S. Acc. Chem. Res. 2003; 36: 342

95 Kotha S, Lahiri K. Bioorg. Med. Chem. Lett. 2001; 11: 2887
96 Kotha S, Lahiri K. Biopolymers 2003; 69: 517
97 Kotha S, Ghosh AK. Synthesis 2004; 558
98 Kotha S, Halder S, Lahiri K. Synthesis 2002; 339
99 Kotha S, Kashinath D. Synthesis 2005; 971
100 Kotha S, Srinivas V, Krishna NG. Heterocycles 2012; 86: 1555

101a Sauers RR, Zampino M, Stockl M, Ferentz J, Shams H. J. Org. Chem. 1983; 48: 1862
101b Mlinarić-Majerski K, Veljković J, Marchand AP, Ganguly B. Tetrahedron 1998; 54: 11381

102 Kotha S, Sreenivasachary N, Deodhar D, Shaikh M. Acta Crystallogr. 2014; 70: 246
103 Handbook of Reagents for Organic Synthesis: Sulfur-Containing Reagents. Paquette LA. John Wiley & Sons; Chichester: 2009

104a Yuan W.-C, Yang L, Zhao J.-Q, Du H.-Y, Wang Z.-H, You Y, Zhang Y.-P, Liu J, Zhang W, Zhou M.-Q. Org. Lett. 2022; 24: 4603
104b Chen X.-L, Wang H.-Y, Wu C.-Y, Tang B.-C, Hu Y.-L, Ma J.-T, Zhuang S.-Y, Yu Z.-C, Wu Y.-D, Wu A.-X. Org. Lett. 2022; 24: 7659
104c Wu Y.-H, Li C.-J, Wei Z.-L, Liao W.-W. Org. Lett. 2022; 24: 9112
104d Mitsudo K, Okumura Y, Yohena K, Kurimoto Y, Sato E, Suga S. Org. Lett. 2023; 25: 3476
104e Qi Z, Wen S, Liu S, Jiang D. Org. Lett. 2023; 25: 7322
104f Li H, Zhang Y, Zou X, Yang X, Zhou P, Ma X, Lu S, Sun Q, Shu C. ACS Catal. 2024; 14: 3664
104g Wang L, Shen Y.-T, Wang Y.-X, Wang H.-Y, Hao W.-J, Jiang B. Adv. Synth. Catal. 2023; 365: 1693
104h Li H, Zhang Y, Yang X, Deng Z, Zhu Z, Zhou P, Ouyang X, Yuan Y, Chen X, Yang L, Liu M, Shu C. Angew. Chem. Int. Ed. 2023; 62: e202300159
104i Jia X, Huang C, Zhang X, Lian Z. Org. Chem. Front. 2021; 8: 5310
104j Qin X.-Y, He L, Li J, Hao W.-J, Tu S.-J, Jiang B. Chem. Commun. 2019; 55: 3227
104k Yan J, Cheo HW, Teo WK, Shi X, Wu H, Idres SB, Deng L.-W, Wu J. J. Am. Chem. Soc. 2020; 142: 11357
104l Singh M, Jamra R, Paul AK, Malakar CC, Singh V. Asian J. Org. Chem. 2022; 11: e202100653
104m Sharma S, Singh D, Kumar S, Vaishali, Jamra R, Banyal N, Deepika, Malakar CC, Singh V. Beilstein J. Org. Chem. 2023; 19: 231
104n Deepika, Paul AK, Malakar CC, Bansal A, Singh V. Asian J. Org. Chem. 2023; 12: e202300289
104o Malakar CC, Merisor E, Conrad J, Beifuss U. Synlett 2010; 1766
104p Putta VP. R. K, Vodnala N, Gujjarappa R, Tyagi U, Garg A, Gupta S, Pujar PP, Malakar CC. J. Org. Chem. 2020; 85: 380
104q Reetu R, Gujjarappa R, Malakar CC. Asian J. Org. Chem. 2022; 11: e202200163
104r Putta VP. R. K, Gujjarappa R, Tyagi U, Pujar PP, Malakar CC. Org. Biomol. Chem. 2019; 17: 2516
104s Kaldhi D, Vodnala N, Gujjarappa R, Nayak S, Ravichandiran V, Gupta S, Hazra CK, Malakar CC. Tetrahedron Lett. 2019; 60: 223
104t Yadav VK, Srivastava VP, Yadav LD. S. Tetrahedron Lett. 2018; 59: 252
104u Sharma S, Malakar CC, Singh V. Asian J. Org. Chem. 2020; 9: 1857
104v Kant K, Patel CK, Banerjee S, Naik P, Atta AK, Kabi AK, Malakar CC. ChemistrySelect 2023; 8: e202303988
104w Putta VP. R. K, Polina S, Gujjarappa R, Kishore PS, Malakar CC, Pujar PP. Polycyclic Aromat. Compd. 2023; 43: 7416
104x Gujjarappa R, Kabi AK, Sravani S, Garg A, Vodnala N, Tyagi U, Kaldhi D, Gupta S, Malakar CC. Overview on Biological Activities of Thiazole Derivatives. In Nanostructured Biomaterials (Materials Horizons: From Nature to Nanomaterials). Swain BP. Springer Nature; Singapore: 2022: 135-227