Skip to main content
Log in

Isocyanide-Based Multicomponent Reactions in Water: Advanced Green Tools for the Synthesis of Heterocyclic Compounds

  • Review
  • Published:
Topics in Current Chemistry Aims and scope Submit manuscript

Abstract

Reaction rate acceleration using green methods is an intriguing area of research for chemists. In this regard, water as a “green solvent” plays a crucial role in the acceleration of some organic transformations and reveals exclusive selectivity and reactivity in comparison with conventional organic solvents. In particular, multicomponent reactions (MCRs) as sustainable tools lead to the rapid generation of small-molecule libraries in water and aqueous media due to the prominent role of the hydrophobic effect. MCRs, as diversity-oriented synthesis (DOS) methods, have great efficiency with simple operations, atom, pot, and step economy synthesis, and mechanistic beauty. Among diverse classes of MCRs, isocyanide-based multicomponent reactions (I-MCRs), as sustainable and versatile reactions, have gained considerable attention in the synthesis of diverse heterocycle rings, especially in drug design because of the peculiar nature of isocyanide as a particular active reactant. I-MCRs that are performed in water are mild, environmentally friendly, and easily controlled, and have a reduced number of workup, purification, and extraction steps, which fit well with the advantages of “green” chemistry. Performing these powerful organic transformations in water and aqueous media is accompanied by acceleration owing to negative activation volumes, which originate from connecting several reactants together to generate a single product. It should be noted that the combination of MCR strategy and aqueous phase reaction is of growing interest for the development of sustainable synthetic techniques in organic conversions. However, an exclusive account focusing on the recent progress in eco-friendly I-MCRs for the construction of heterocycles in water and aqueous media is particularly lacking. This review highlights the progress of various kinds of I-MCRs in water and aqueous media as benign methods for the efficient construction of vital heterocyclic scaffolds, with a critical discussion of the subject in the period 2000–2021. We hope that this themed collection will be of interest and beneficial for organic and pharmaceutical chemists and will inspire more reaction development in this fascinating field.

Graphical Abstract

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Scheme 1
Scheme 2
Scheme 3
Fig. 7
Fig. 8
Scheme 4
Scheme 5
Scheme 6
Fig. 9
Fig. 10
Scheme 7
Scheme 8
Scheme 9
Scheme 10
Scheme 11
Scheme 12
Scheme 13
Scheme 14
Fig. 11
Fig. 12
Scheme 15
Scheme 16
Scheme 17
Fig. 13
Fig. 14
Scheme 18
Scheme 19
Scheme 20
Scheme 21
Scheme 22
Scheme 23
Scheme 24
Scheme 25
Scheme 26
Scheme 27
Scheme 28
Scheme 29
Scheme 30
Fig. 15
Scheme 31
Scheme 32
Scheme 33
Scheme 34
Fig. 16
Scheme 35
Scheme 36
Scheme 37
Scheme 38
Scheme 39
Scheme 40
Scheme 41
Fig. 17
Fig. 18
Scheme 42
Scheme 43
Scheme 44
Scheme 45
Scheme 46
Scheme 47
Scheme 48
Scheme 49
Scheme 50
Scheme 51
Fig. 19
Scheme 52
Scheme 53
Scheme 54
Scheme 55
Fig. 20
Fig. 21
Scheme 56
Scheme 57
Scheme 58
Scheme 59
Scheme 60
Scheme 61

Similar content being viewed by others

References

  1. Gomtsyan A (2012) Chem Heterocycl Compd 48:7

    Article  CAS  Google Scholar 

  2. Eftekhari-Sis B, Zirak M, Akbari A (2013) Chem Rev 113:2958

    Article  PubMed  CAS  Google Scholar 

  3. Al-Mulla A (2017) Der Pharma Chem 9:141

    CAS  Google Scholar 

  4. Atkin T, Comai S, Gobbi G (2018) Pharmacol Rev 70:197

    Article  PubMed  CAS  Google Scholar 

  5. Ahmad S, Alam O, Naim MJ, Shaquiquzzaman M, Alam MM, Iqbal M (2018) Eur J Med Chem 157:527

    Article  PubMed  CAS  Google Scholar 

  6. Katsuyama A, Yakushiji F, Ichikawa S (2018) J Org Chem 83:7085

    Article  PubMed  CAS  Google Scholar 

  7. Znabet A, Polak MM, Janssen E, de Kanter FJ, Turner NJ, Orru RV, Ruijter E (2010) Chem Commun 46:7918

    Article  CAS  Google Scholar 

  8. Zarganes-Tzitzikas T, Dömling A (2014) Org Chem Front 1:834

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  9. Zarganes-Tzitzikas T, Neochoritis CG, Dömling A (2019) ACS Med Chem Lett 10:389

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  10. Shaabani A, Maleki A, Rezayan AH, Sarvary A (2011) Mol Divers 15:41

    Article  PubMed  CAS  Google Scholar 

  11. Farhid H, Nazeri MT, Shaabani A, Armaghan M, Janiak C (2021) Amino Acids 53:1

    Article  PubMed  CAS  Google Scholar 

  12. Farhid H, Rostami MM, Shaabani A, Notash B (2021) SynOpen 5:167

    Article  CAS  Google Scholar 

  13. Rudick JG, Shaabani S, Dömling A (2020) Front Chem 7:918

    Article  PubMed  PubMed Central  Google Scholar 

  14. Javanbakht S, Nazeri MT, Shaabani A, Ghorbani M (2020) Int J Biol Macromol 164:2873

    Article  PubMed  CAS  Google Scholar 

  15. Rideout DC, Breslow R (1980) J Am Chem Soc 102:7816

    Article  CAS  Google Scholar 

  16. Butler RN, Coyne AG (2010) Chem Rev 110:6302

    Article  PubMed  CAS  Google Scholar 

  17. Jung Y, Marcus R (2007) J Am Chem Soc 129:5492

    Article  PubMed  CAS  Google Scholar 

  18. Lubineau A (1986) J Org Chem 51:2142

    Article  CAS  Google Scholar 

  19. Lubineau A, Augé J, Queneau Y (1994) Synthesis 1994:741

    Article  Google Scholar 

  20. Pirrung MC, Sarma KD (2004) J Am Chem Soc 126:444

    Article  PubMed  CAS  Google Scholar 

  21. Shapiro N, Vigalok A (2008) Angew Chem Int Ed 47:2849

    Article  CAS  Google Scholar 

  22. Chanda A, Fokin VV (2009) Chem Rev 109:725

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  23. Kumaravel K, Vasuki G (2009) Curr Org Chem 13:1820

    Article  CAS  Google Scholar 

  24. Rahmati A, Pashmforoush N (2015) J Iran Chem Soc 12:993

    Article  CAS  Google Scholar 

  25. Padwa A, Kinder FR (1990) Prog Heterocycl Chem Critical Rev 2:22

    Article  CAS  Google Scholar 

  26. Bergmeier SC, Lapinsky DJ (2013) Prog Heterocycl Chem 20:47

    Article  Google Scholar 

  27. Nazeri MT, Nasiriani T, Farhid H, Javanbakht S, Bahri F, Shadi M, Shaabani A (2022) ACS Sustain Chem Eng 10:8115

    Article  CAS  Google Scholar 

  28. Ovat A, Muindi F, Fagan C, Brouner M, Hansell E, Dvorák J, Sojka D, Kopácek P, McKerrow JH, Caffrey CR (2009) J Med Chem 52:7192

    Article  PubMed  CAS  Google Scholar 

  29. Zhao GL, Ibrahem I, Sunden H, Cordova A (2007) Adv Synth Catal 349:1210

    Article  CAS  Google Scholar 

  30. Amatore M, Beeson TD, Brown SP, MacMillan DW (2009) Angew Chem Int Ed 121:5223

    Article  Google Scholar 

  31. De Fusco C, Tedesco C, Lattanzi A (2011) J Org Chem 76:676

    Article  PubMed  Google Scholar 

  32. Deobald AM, Corrêa AG, Rivera DG, Paixão MW (2012) Org Biomol Chem 10:7681

    Article  PubMed  CAS  Google Scholar 

  33. Yudin AK (2006) Aziridines and Epoxides in Organic Synthesis. Wiley, New York

    Book  Google Scholar 

  34. Rotstein BH, Zaretsky S, Rai V, Yudin AK (2014) Chem Rev 114:8323

    Article  PubMed  CAS  Google Scholar 

  35. dos Santos DA, da Silva AR, Ellena J, da Silva CC, Paixao MW, Correa AG (2020) Synthesis 52:1076

    Article  Google Scholar 

  36. Malarney KP, Shekhar K, Schmidt VA (2021) Org Biomol Chem 19:8425

    Article  PubMed  CAS  Google Scholar 

  37. Im C, Maiti SN, Micetich RG, Daneshxalab M, Atchison K, Phillips OA, Kunugita C (1994) J Antibiot Res 47:1030

    Article  CAS  Google Scholar 

  38. Delpiccolo CM, Mata EG (2004) Tetrahedron Lett 45:4085

    Article  CAS  Google Scholar 

  39. Banik BK, Becker FF, Banik I (2004) Bioorg Med Chem 12:2523

    Article  PubMed  CAS  Google Scholar 

  40. Ugi I (1982) Angew Chem Int Ed Engl 21:810

    Article  Google Scholar 

  41. Hulme C, Dietrich J (2009) Mol Divers 13:195

    Article  PubMed  CAS  Google Scholar 

  42. Basso A, Banfi L, Riva R, Guanti G (2004) Tetrahedron Lett 45:587

    Article  CAS  Google Scholar 

  43. Kanizsai I, Szakonyi Z, Sillanpää R, Fülöp F (2006) Tetrahedron Lett 47:9113

    Article  CAS  Google Scholar 

  44. Kanizsai I, Gyónfalvi S, Szakonyi Z, Sillanpää R, Fülöp F (2007) Green Chem 9:357

    Article  CAS  Google Scholar 

  45. Szakonyi Z, Sillanpää R, Fülöp F (2010) Mol Divers 14:59

    Article  PubMed  CAS  Google Scholar 

  46. Morioka H, Takezawa M, Shibai H, Okawara T, Furukawa M (1986) Agr Biol Chem 50:1757

    CAS  Google Scholar 

  47. Abdel-Ghaffar S, Mpango G, Ismail M, Nanyonga S (2002) Boll Chim Farm 141:389

    PubMed  CAS  Google Scholar 

  48. Naskar D, Roy A, Seibel WL, West L, Portlock DE (2003) Tetrahedron Lett 44:6297

    Article  CAS  Google Scholar 

  49. Hollis A, Ahmed Z (2013) N Engl J Med 369:2474

    Article  PubMed  CAS  Google Scholar 

  50. Shaabani A, Nazeri MT, Afshari R (2019) Mol Divers 23:751

    Article  PubMed  CAS  Google Scholar 

  51. Singh KN (2018) Org Biomol Chemm 16:9084

    Article  Google Scholar 

  52. Nazeri MT, Farhid H, Javanbakht S, Shaabani A, Notash B (2020) Synlett 31:965

    Article  CAS  Google Scholar 

  53. Nazeri MT, Shaabani A, Notash B (2021) Org Biomol Chem 19:3722

    Article  PubMed  CAS  Google Scholar 

  54. Shalini K, Sharma PK, Kumar N (2010) Der Chem Sin 1:36

    CAS  Google Scholar 

  55. Zhang M, Neumann H, Beller M (2013) Angew Chem Int Ed 125:625

    Article  Google Scholar 

  56. Kaur R, Rani V, Abbot V (2017) J Pharm Chem Chem Sci 20:1

    Google Scholar 

  57. Thomas K, Schmidt MS (2012) New York Times

  58. Simons J (2003) Fortune 147:58

    PubMed  Google Scholar 

  59. Banerjee R, Kumar H, Banerjee M (2015) In J Res Phytochem Pharmacol 5:48

    Google Scholar 

  60. Bandurraga MM, Fenical W, Donovan SF, Clardy J (1982) J Am Chem Soc 104:6463

    Article  CAS  Google Scholar 

  61. Hochlowski JE, Walker RP, Ireland C, Faulkner DJ (1982) J Org Chem 47:88

    Article  CAS  Google Scholar 

  62. Williams D, Andersen RJ, Van Duyne GD, Clardy J (1987) J Org Chem 52:332

    Article  CAS  Google Scholar 

  63. Shiroodi RK, Koleda O, Gevorgyan V (2014) J Am Chem Soc 136:13146

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  64. Okitsu T, Nakata K, Nishigaki K, Michioka N, Karatani M, Wada A (2014) J Org Chem 79:5914

    Article  PubMed  CAS  Google Scholar 

  65. Feist F (1902) Ber Dtsch Chem Ges 35:1537

    Article  CAS  Google Scholar 

  66. Zorba L, Kidonakis M, Saridakis I, Stratakis M (2019) Org Lett 21:5552

    Article  PubMed  CAS  Google Scholar 

  67. Shaabani A, Teimouri MB, Bijanzadeh HR (2002) Tetrahedron Lett 43:9151

    Article  CAS  Google Scholar 

  68. Shaabani A, Teimouri MB, Bijanzadeh HR (2004) Monatsh Chem 135:441

    Article  CAS  Google Scholar 

  69. Shaabani A, Teimouri MB, Bijanzadeh HR (2004) Monatsh Chem 135:589

    Article  CAS  Google Scholar 

  70. Heravi MM, Baghernejad B, Oskooie HA (2009) Mol Divers 13:385

    Article  PubMed  CAS  Google Scholar 

  71. Teimouri MB, Bazhrang R (2008) Monatsh Chem 139:957

    Article  CAS  Google Scholar 

  72. Nair V, Vinod A (2000) Chem. Commun. : 1019.

  73. Azizian J, Mohammadizadeh MR, Mohammadi AA, Karimi AR (2005) Heteroat. Chem In J Main G Elemen 16:259

    CAS  Google Scholar 

  74. Yadav J, Reddy BS, Shubashree S, Sadashiv K, Rao DK (2007) J Mol Catal Chem 272:128

    Article  CAS  Google Scholar 

  75. Ramazani A, Rezaei A, Mahyari AT, Rouhani M, Khoobi M (2010) Helv Chim Acta 93:2033

    Article  CAS  Google Scholar 

  76. Zarganes-Tzitzikas T, Chandgude AL, Dömling A (2015) Chem Rec 15:981

    Article  PubMed  CAS  Google Scholar 

  77. Hooshmand SE, Ghadari R, Mohammadian R, Shaabani A, Khavasi HR (2019) ChemistrySelect 4:11893

    Article  CAS  Google Scholar 

  78. Nazeri MT, Mohammadian R, Farhid H, Shaabani A, Notash B (2020) Tetrahedron Lett 61:151408

    Article  CAS  Google Scholar 

  79. Adib M, Sheikhi E, Kavoosi A, Bijanzadeh HR (2010) Tetrahedron 66:9263

    Article  CAS  Google Scholar 

  80. El Kaïm L, Grimaud L, Oble J (2005) Angew Chem 117:8175

    Article  Google Scholar 

  81. El Kaim L, Grimaud L (2014) Eur J Org Chem 2014:7749

    Article  Google Scholar 

  82. Vessally E, Ramazani A, Shabrendi H, Ghadimi R, Rouhani M (2013) J Chem 20:13

    Google Scholar 

  83. Adib M, Mahdavi M, Bagherzadeh S, Zhu L-G, Rahimi-Nasrabadi M (2010) Tetrahedron Lett 51:27

    Article  CAS  Google Scholar 

  84. Safaei HR, Shioukhi N, Shekouhy M (2013) Monatsh Chem 144:1855

    Article  CAS  Google Scholar 

  85. Safaei HR, Shekouhy M (2017) Acta Chim Slov 64:1020

    Article  PubMed  CAS  Google Scholar 

  86. Ohi N, Sato N, Soejima M, Doko T, Terauchi T, Naoe Y, Motoki T (2008) Google Patents

  87. Tai TB, Huong VTT, Nguyen MT (2014) Struct Bond React Heterocyclic Cmpd 20:161

    Article  Google Scholar 

  88. Bhardwaj V, Gumber D, Abbot V, Dhiman S, Sharma P (2015) Rsc Adv 5:15233

    Article  CAS  Google Scholar 

  89. Di Santo R, Tafi A, Costi R, Botta M, Artico M, Corelli F, Forte M, Caporuscio F, Angiolella L, Palamara AT (2005) J Med Chem 48:5140

    Article  PubMed  Google Scholar 

  90. Bauer JD, King RW, Brady SF (2010) J Nat Prod 73:976

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  91. Avendaño C, Menéndez JC (2004) Med Chem Rev 1:419

    Google Scholar 

  92. Andrieux CP, Audebert P, Hapiot P, Saveant JM (1991) J Phys Chem 95:10158

    Article  CAS  Google Scholar 

  93. Alasalvar C, Shahidi F, Cadwallader KR (2003) J Agric Food Chem 51:5067

    Article  PubMed  CAS  Google Scholar 

  94. Hantzsch A (1890) Ber Dtsch Chem Ges 23:1474

    Article  Google Scholar 

  95. Paal C (1885) Ber Dtsch Chem Ges 18:367

    Article  Google Scholar 

  96. Pandey PS, Rao TS (2004) Bioorg Med Chem Lett 14:129

    Article  PubMed  CAS  Google Scholar 

  97. Knorr L (1884) Ber Dtsch Chem Ges 17:2863

    Article  Google Scholar 

  98. Nazeri MT, Shaabani A (2021) New J Chem 45:21967

    Article  CAS  Google Scholar 

  99. Nazeri MT, Nowee AB, Shaabani A (2021) New J Chem 45:3479

    Article  CAS  Google Scholar 

  100. Kolontsova AN, Ivantsova MN, Tokareva MI, Mironov MA (2010) Mol Divers 14:543

    Article  PubMed  CAS  Google Scholar 

  101. Pagadala R, Kommidi DR, Kankala S, Maddila S, Singh P, Moodley B, Koorbanally N, Jonnalagadda SB (2015) Org Biomol Chem 13:1800

    Article  PubMed  CAS  Google Scholar 

  102. Pagadala R, Anugu S (2018) J Heterocycl Chem 55:181

    Article  CAS  Google Scholar 

  103. Lu K, Ding F, Qin L, Jia X, Xu C, Zhao X, Yao Q, Yu P (2016) Chem Asian J 11:2121

    Article  PubMed  CAS  Google Scholar 

  104. Lázár L, Nagy M, Rácz D, Zsuga M, Kéki S (2014) Tetrahedron 70:3691

    Article  Google Scholar 

  105. Revill C, Serradell N, Bolos J, Rosa E (2007) Drug Future 32:788

    Article  CAS  Google Scholar 

  106. Njoroge FG, Chen KX, Shih N-Y, Piwinski JJ (2008) Acc Chem Res 41:50

    Article  PubMed  CAS  Google Scholar 

  107. Zhu X, Xu X-P, Sun C, Wang H-Y, Zhao K, Ji S-J (2010) J Comb Chem 12:822

    Article  PubMed  CAS  Google Scholar 

  108. Yuan R, Li M-Q, Ren X-X, Chen W, Zhou H, Wan Y, Zhang P, Wu H (2020) Res Chem Int 46:2275

    Article  CAS  Google Scholar 

  109. Stepankova V, Damborsky J, Chaloupkova R (2013) Biotechnol J 8:719

    Article  PubMed  CAS  Google Scholar 

  110. Wang H-Y, Bao M, Jiang B, Li L (2016) RSC Adv 6:6459

    Article  CAS  Google Scholar 

  111. Yugandhar D, Srivastava AK (2015) ACS Comb Sci 17:474

    Article  PubMed  CAS  Google Scholar 

  112. Jiang H, Tian Y, Tian L, Li J (2017) RSC Adv 7:32300

    Article  CAS  Google Scholar 

  113. Santra S, Andreana PR (2007) Org Lett 9:5035

    Article  PubMed  CAS  Google Scholar 

  114. Santra S, Andreana PR (2011) Angew Chem 123:9590

    Article  Google Scholar 

  115. Ziarani GM, Moradi R, Ahmadi T, Lashgari N (2018) RSC Adv 8:12069

    Article  Google Scholar 

  116. Humphrey GR, Kuethe JT (2006) Chem Rev 106:2875

    Article  PubMed  CAS  Google Scholar 

  117. Shafakat Ali NA, Ahmad Dar B, Pradhan V, Farooqui M (2013) Mini Rev Med Chem 13:1792

    Article  PubMed  CAS  Google Scholar 

  118. Dai Q, Jiang Y, Guo S, Yu J-T, Cheng J (2015) Chem Commun 51:14781

    Article  CAS  Google Scholar 

  119. Kiamehr M, Moghaddam FM, Erami MS (2015) Tetrahedron Lett 56:7190

    Article  CAS  Google Scholar 

  120. Grimmett M, Katritzky A, Rees C (1984) Pergamon Press, New York, vol 5, p 345

  121. Luca LD (2006) Curr Med Chem 13:1

    PubMed  Google Scholar 

  122. Brimblecombe R, Duncan W, Durant G, Emmett J, Ganellin C, Parsons M (1975) J Int Med Res 3:86

    Article  CAS  Google Scholar 

  123. Dyck B, Goodfellow VS, Phillips T, Grey J, Haddach M, Rowbottom M, Naeve GS, Brown B, Saunders J (2004) Bioorg Med Chem Lett 14:1151

    Article  PubMed  CAS  Google Scholar 

  124. Kumar Gupta G, Rani N, Kumar V (2012) Mini-Rev Org Chem 9:270

    Article  Google Scholar 

  125. Boltjes A, Dömling A (2019) Eur J Org Chem 2019:7007

    Article  CAS  Google Scholar 

  126. Li C-J (2005) Chem Rev 105:3095

    Article  PubMed  CAS  Google Scholar 

  127. Adib M, Mahdavi M, Noghani MA, Mirzaei P (2007) Tetrahedron Lett 48:7263

    Article  CAS  Google Scholar 

  128. Rostami ME, Gorji B, Zadmard R (2018) Tetrahedron Lett 59:2393

    Article  Google Scholar 

  129. Katsuyama A, Matsuda A, Ichikawa S (2016) Org Lett 18:2552

    Article  PubMed  CAS  Google Scholar 

  130. Shaabani S, Xu R, Ahmadianmoghaddam M, Gao L, Stahorsky M, Olechno J, Ellson R, Kossenjans M, Helan V, Dömling A (2019) Green Chem 21:225

    Article  PubMed  CAS  Google Scholar 

  131. Fascio ML, Errea MI, D’accorso NB (2015) Eur J Org Chem 90:666

    CAS  Google Scholar 

  132. Tabassum K, Ekta P, Kavitkumar P (2018) Mini-Rev Org Chem 15:459

    Article  CAS  Google Scholar 

  133. Güzeldemirci NU, Küçükbasmacı Ö (2010) Eur J Med Chem 45:63

    Article  PubMed  Google Scholar 

  134. Gürsoy E, Güzeldemirci NU (2007) Eur J Med Chem 42:320

    Article  PubMed  Google Scholar 

  135. Demjén A, Gyuris M, Wölfling J, Puskás LG, Kanizsai I (2014) Beilstein J Org Chem 10:2338

    Article  PubMed  PubMed Central  Google Scholar 

  136. Tailor YK, Khandelwal S, Kumari Y, Awasthi K, Kumar M (2015) RSC Adv 5:46415

    Article  CAS  Google Scholar 

  137. Nazeri MT, Nowee AB, Javanbakht S, Farhid H, Shaabani A, Notash B (2021) Tetrahedron 132:243

    Google Scholar 

  138. Mohite P, Bhaskar V (2011) In J Pharm Tech Res 3:1557

    CAS  Google Scholar 

  139. Neochoritis CG, Zhao T, Dömling A (2019) Chem Rev 119:1970

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  140. Ugi I, Meyr R (1961) Chem Ber 94:2229

    Article  CAS  Google Scholar 

  141. Patil P, de Haan M, Kurpiewska K, Kalinowska-Tłuścik J, Dömling A (2016) ACS Comb Sci 18:170

    Article  PubMed  CAS  Google Scholar 

  142. Chandgude AL, Dömling A (2016) Green Chem 18:3718

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  143. Borisov RS, Voskressensky LG, Polyakov AI, Borisova TN, Varlamov AV (2014) Synlett 25:955

    Article  CAS  Google Scholar 

  144. Borisov RS, Polyakov AI, Medvedeva LA, Khrustalev VN, Guranova NI, Voskressensky LG (2010) Org Lett 12:3894

    Article  PubMed  CAS  Google Scholar 

  145. Borisov R, Polyakov A, Medvedeva L, Guranova N, Voskressensky L (2012) Russ Chem Bull 61:1609

    Article  CAS  Google Scholar 

  146. Yerande SG, Newase KM, Singh B, Boltjes A, Dömling A (2014) Tetrahedron Lett 55:3263

    Article  CAS  Google Scholar 

  147. Patil P, Kurpiewska K, Kalinowska-Tłuścik J, Dömling A (2017) ACS Comb Sci 19:343

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  148. Mishra R, Jha K, Kumar S, Tomer I (2011) Der Pharma Chem 3:38

    CAS  Google Scholar 

  149. Moghaddam FM, Bardajee GR, Dolabi M (2010) J Sulfur Chem 31:387

    Article  CAS  Google Scholar 

  150. Moghaddam FM, Khodabakhshi MR, Latifkar A (2014) Tetrahedron Lett 55:1251

    Article  Google Scholar 

  151. Vaidya A, Jain S, Jain P, Jain P, Tiwari N, Jain R, Jain R, Jain K, Agrawal KR (2016) Mini Prev Med Chem 16:825

    Article  CAS  Google Scholar 

  152. Palacios F, Alonso C, Aparicio D, Rubiales G, Jesús M (2007) Tetrahedron 63:523

    Article  CAS  Google Scholar 

  153. Jafari A, Ramazani A, Sadri F, Joo SW (2016) Phosphorus Sulfur Silicon Relat Elem 191:316

    Article  CAS  Google Scholar 

  154. Jafari A, Ramazani A, Asiabi PA, Sadri F, Joo SW (2015) Phosphorus Sulfur Silicon Relat Elem 190:2246

    Article  CAS  Google Scholar 

  155. Jafari A, Ramazani A, Ahankar H, Asiabi PA, Sadri F, Joo SW (2016) Phosphorus Sulfur Silicon Relat Elem 191:373

    Article  CAS  Google Scholar 

  156. Zhu J, Mo J, Lin H-z, Chen Y, Sun H-p (2018) Bioorg Med Chem 26:3065

    Article  PubMed  CAS  Google Scholar 

  157. Adib M, Mahdavi M, Ansari S, Malihi F, Zhu L-G, Bijanzadeh HR (2009) Tetrahedron Lett 50:7246

    Article  CAS  Google Scholar 

  158. Davyt D, Serra G (2010) Mar Drugs 8:2755

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  159. Alom N-E, Wu F, Li W (2017) Org Lett 19:930

    Article  PubMed  CAS  Google Scholar 

  160. Shaabani A, Hooshmand SE (2018) Ultrason Sonochem 40:84

    Article  PubMed  CAS  Google Scholar 

  161. Bauer M, Maurer F, Hoffmann SM, Kazmaier U (2008) Synlett 2008:3203

    Article  Google Scholar 

  162. Cinelli MA, Morrell A, Dexheimer TS, Scher ES, Pommier Y, Cushman M (2008) J Med Chem 51:4609

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  163. Nakao Y, Idei H, Kanyiva KS, Hiyama T (2009) J Am Chem Soc 131:15996

    Article  PubMed  CAS  Google Scholar 

  164. Bossert F, Meyer H, Wehinger E (1981) Angew Chem Int Ed Engl 20:762

    Article  Google Scholar 

  165. Padwa A, Heidelbaugh TM, Kuethe JT (2000) J Org Chem 65:2368

    Article  PubMed  CAS  Google Scholar 

  166. Singh KN (2021) Org Biomol Chem 19:2622

    Article  Google Scholar 

  167. Xiao C, Li Y, Lun H, Cui C, Xu Y (2013) J Solid State Chem 208:127

    Article  CAS  Google Scholar 

  168. Fan Z, Ni J, Zhang A (2016) J Am Chem Soc 138:8470

    Article  PubMed  CAS  Google Scholar 

  169. Moore P, Evenson A, Luckey T, McCoy E, Elvehjem C, Hart E (1946) J Biol Chem 165:437

    Article  PubMed  CAS  Google Scholar 

  170. Carta A, Corona P, Loriga M (2005) Curr Med Chem 12:2259

    Article  PubMed  CAS  Google Scholar 

  171. Carta A, Paglietti G, Nikookar MER, Sanna P, Sechi L, Zanetti S (2002) Eur J Med Chem 37:355

    Article  PubMed  CAS  Google Scholar 

  172. Jaso A, Zarranz B, Aldana I, Monge A (2003) Eur J Med Chem 38:791

    Article  PubMed  CAS  Google Scholar 

  173. Das U, Pati HN, Panda AK, De Clercq E, Balzarini J, Molnár J, Baráth Z, Ocsovszki I, Kawase M, Zhou L (2009) Bioorg Med Chem 17:3909

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  174. Krasavin M, Parchinsky V, Shumsky A, Konstantinov I, Vantskul A (2010) Tetrahedron Lett 51:1367

    Article  CAS  Google Scholar 

  175. Mironov MA, Ivantsova MN, Mokrushin VS (2003) Mol Divers 6:193

    Article  PubMed  CAS  Google Scholar 

  176. Shaabani A, Hajishaabanha F, Mofakham H, Mahyari M, Lali B (2012) Helv Chim Acta 95:246

    Article  CAS  Google Scholar 

  177. Asgari MS, Sepehri S, Bahadorikhalili S, Ranjbar PR, Rahimi R, Gholami A, Kazemi A, Khoshneviszadeh M, Larijani B, Mahdavi M (2020) Chem Heterocycl Compd 56:488

    Article  CAS  Google Scholar 

  178. Seitz LE, Suling WJ, Reynolds RC (2002) J Med Chem 45:5604

    Article  PubMed  CAS  Google Scholar 

  179. Kolla SR, Lee YR (2010) Tetrahedron 66:8938

    Article  CAS  Google Scholar 

  180. Shaabani A, Shaabani S, Seyyedhamzeh M, Sangachin MH, Hajishaabanha F (2016) Res Chem Intermed 42:7247

    Article  CAS  Google Scholar 

  181. Edayadulla N, Lee YR (2014) RSC Adv 4:11459

    Article  CAS  Google Scholar 

  182. Ayati A, Daraie M, Heravi MM, Tanhaei B (2017) Iran J Catal 7:193

    CAS  Google Scholar 

  183. Gujjarappa R, Vodnala N, Malakar CC (2020) Adv Synth Catal 362:4896

    Article  CAS  Google Scholar 

  184. Liu SJ, Zhao Q, Chen RF, Deng Y, Fan QL, Li FY, Wang LH, Huang CH, Huang W (2006) Chem Eur J 12:4351

    Article  PubMed  CAS  Google Scholar 

  185. Collado D, Perez-Inestrosa E, Suau R, Desvergne J-P, Bouas-Laurent H (2002) Org Lett 4:855

    Article  PubMed  CAS  Google Scholar 

  186. Durola F, Sauvage J-P, Wenger OS (2006) Chem Commun 1:171

    Article  Google Scholar 

  187. Sinha MK, Khoury K, Herdtweck E, Dömling A (2013) Chemistry, vol 19. Weinheim an der Bergstrasse, Germany, p 8048

    Google Scholar 

  188. Goel P, Alam O, Naim MJ, Nawaz F, Iqbal M, Alam MI (2018) Eur J Med Chem 157:480

    Article  PubMed  CAS  Google Scholar 

  189. Tanaka N, Suto S, Ishiyama H, Kubota T, Yamano A, Shiro M, Fromont J, Ji K (2012) Org Lett 14:3498

    Article  PubMed  CAS  Google Scholar 

  190. Senejoux F, Evanno L, Poupon E (2013) Eur J Org Chem 2013:453

    Article  CAS  Google Scholar 

  191. Parmenon C, Guillard J, Caignard D-H, Hennuyer N, Staels B, Audinot-Bouchez V, Boutin J-A, Dacquet C, Ktorza A, Viaud-Massuard M-C (2008) Bioorg Med Chem Lett 18:1617

    Article  PubMed  CAS  Google Scholar 

  192. Li Y, Miao T, Li P, Wang L (2018) Org Lett 20:1735

    Article  PubMed  CAS  Google Scholar 

  193. Atwal KS, Swanson BN, Unger SE, Floyd DM, Moreland S, Hedberg A, O’Reilly BC (1991) J Med Chem 34:806

    Article  PubMed  CAS  Google Scholar 

  194. Deres K, Schröder CH, Paessens A, Goldmann S, Hacker HJ, Weber O, Krämer T, Niewöhner U, Pleiss U, Stoltefuss J (2003) Science 299:893

    Article  PubMed  CAS  Google Scholar 

  195. Yavari I, Karimi E, Djahaniani H (2007) Synth Commun 37:2593

    Article  CAS  Google Scholar 

  196. Shinde VV, Jung S (2019) Tetrahedron 75:778

    Article  CAS  Google Scholar 

  197. Wang JL (2000) Proc Natl Acad Sci USA 97:7124

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  198. Kumar D, Reddy VB, Sharad S, Dube U, Kapur S (2009) Eur J Med Chem 44:3805

    Article  PubMed  CAS  Google Scholar 

  199. Martínez-Grau A, Marco J (1997) Bioorg Med Chem Lett 7:3165

    Article  Google Scholar 

  200. Saini A, Kumar S, Sandhu JS (2006) Synlett 2006:1928

    Article  Google Scholar 

  201. Sarma R, Sarmah MM, Lekhok KC, Prajapati D (2010) Synlett 28:47

    Google Scholar 

  202. Akbari A, Azami-Sardooei Z, Hosseini-Nia A (2013) J Korean Chem Soc 57:455

    Article  CAS  Google Scholar 

  203. Soleimani E, Ghorbani S, Ghasempour HR (2013) Tetrahedron 69:8511

    Article  CAS  Google Scholar 

  204. Soleimani E, Torkaman S, Sepahvand H, Ghorbani S (2019) Mol Divers 23:739

    Article  PubMed  CAS  Google Scholar 

  205. Ishida H, Agag T (2011) Handbook of benzoxazine resins. Elsevier, New York

    Google Scholar 

  206. Shafiee S (2018) Iran J Org Chem 4:2483

    Google Scholar 

  207. Ajani OO (2012) Arch Pharm 345:841

    Article  CAS  Google Scholar 

  208. Yadav N, Sagir H, Ansari MD, Siddiqui I (2018) Catal Lett 148:1676

    Article  CAS  Google Scholar 

  209. Sagir H, Rai P, Singh PK, Siddiqui I (2016) New J Chem 40:6819

    Article  CAS  Google Scholar 

  210. Velasco-Rubio Á, Varela JA, Saá C (2020) Adv Synth Catal 362:4861

    Article  CAS  Google Scholar 

  211. Saranya PV, Neetha M, Radhika S, Anilkumar G (2021) Adv Synth Catal 58:673

    CAS  Google Scholar 

  212. Farhid H, Nazeri MT, Rostami MM, Shaabani A, Notash B (2022) Chem Pap 76:987

    Article  CAS  Google Scholar 

  213. Chen Y, Le V, Xu X, Shao X, Liu J, Li Z (2014) Bioorg Med Chem Lett 24:3948

    Article  PubMed  CAS  Google Scholar 

  214. Parmar NJ, Barad HA, Pansuriya BR, Teraiya SB, Gupta VK, Kant R (2012) Bioorg Med Chem Lett 22:3816

    Article  PubMed  CAS  Google Scholar 

  215. Lelais G, Epple R, Marsilje TH, Long YO, McNeill M, Chen B, Lu W, Anumolu J, Badiger S, Bursulaya B (2016) J Med Chem 59:6671

    Article  PubMed  CAS  Google Scholar 

  216. Breitenlechner CB, Wegge T, Berillon L, Graul K, Marzenell K, Friebe W-G, Thomas U, Schumacher R, Huber R, Engh RA (2004) J Med Chem 47:1375

    Article  PubMed  CAS  Google Scholar 

  217. Banfi L, Basso A, Lambruschini C, Moni L, Riva R (2017) Chem Heterocycl Compd 53:382

    Article  CAS  Google Scholar 

  218. Vitaku E, Smith DT, Njardarson JT (2014) J Med Chem 57:10257

    Article  PubMed  CAS  Google Scholar 

  219. Malki Y, Martinez J, Masurier N (2021) Med Res Rev 41:2247

    Article  PubMed  CAS  Google Scholar 

  220. Arora N, Dhiman P, Kumar S, Singh G, Monga V (2020) Bioorg Chem 97:103668

    Article  PubMed  CAS  Google Scholar 

  221. Nazeri MT, Farhid H, Mohammadian R, Shaabani A (2020) ACS Comb Sci 22:361

    Article  PubMed  CAS  Google Scholar 

  222. Malki Y, Maillard LT, Masurier N (2022) Eur J Org Chem 2022:e202100492

    Article  CAS  Google Scholar 

  223. Farhid H, Khodkari V, Nazeri MT, Javanbakht S, Shaabani A (2021) Org Biomol Chem 19:3318

    Article  PubMed  CAS  Google Scholar 

  224. Shaabani A, Maleki A, Mofakham H, Moghimi-Rad J (2008) J Org Chem 73:3925

    Article  PubMed  CAS  Google Scholar 

  225. Shaabani A, Hezarkhani Z, Faroghi MT (2016) Monatsh Chem 147:1963

    Article  CAS  Google Scholar 

  226. Shaabani A, Sepahvand H, Ghasemi S (2019) Mol Divers 23:585

    Article  PubMed  CAS  Google Scholar 

  227. Shaabani A, Khodkari V, Nazeri MT, Ghasemi S, Mohammadian R, Shaabani S (2019) J Iran Chem Soc 16:1793

    Article  CAS  Google Scholar 

  228. Shaabani A, Mofakham H, Mousavifaraz S (2012) Synlett 23:731

    Article  CAS  Google Scholar 

  229. Polshettiwar V, Varma RS (2008) Acc Chem Res A 41:629

    Article  CAS  Google Scholar 

  230. De Silva RA, Santra S, Andreana PR (2008) Org Lett 10:4541

    Article  PubMed  Google Scholar 

  231. Akbarzadeh R, Amanpour T, Bazgir A (2014) Tetrahedron 70:8142

    Article  CAS  Google Scholar 

  232. Zha G-F, Rakesh K, Manukumar H, Shantharam C, Long S (2019) Eur J Med Chem 162:465

    Article  PubMed  CAS  Google Scholar 

  233. Rasouli MA, Mahdavi M, Ranjbar PR, Saeedi M, Shafiee A, Foroumadi A (2012) Tetrahedron Lett 53:7088

    Article  CAS  Google Scholar 

  234. Yet L (2000) Chem Rev 100:2963

    Article  PubMed  CAS  Google Scholar 

  235. Kulsi G, Ghorai A, Chattopadhyay P (2012) Tetrahedron Lett 53:3619

    Article  CAS  Google Scholar 

Download references

Acknowledgements

This paper has been supported by the Research Council of Shahid Beheshti University and the RUDN University Strategic Academic Leadership Program (A. Shaabani).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Ahmad Shaabani.

Ethics declarations

Conflict of interest

The authors declare no conflict of interest.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Nasiriani, T., Javanbakht, S., Nazeri, M.T. et al. Isocyanide-Based Multicomponent Reactions in Water: Advanced Green Tools for the Synthesis of Heterocyclic Compounds. Top Curr Chem (Z) 380, 50 (2022). https://doi.org/10.1007/s41061-022-00403-8

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1007/s41061-022-00403-8

Keywords

Navigation