How to cite this paper
Zaidi, S., Chaturvedi, A., Singh, N & Chaturvedi, D. (2017). Triton-B catalyzed, efficient and solvent-free approach for the synthesis of dithiocarbamates.Current Chemistry Letters, 6(4), 143-150.
References
1. (a) Lambert C. (2004) Sulphur chemistry in crop protection. J. Sulphur Chem., 25(1) 39-62; (b) Eng G., Song X., Duong Q., Strickman D., Glass J., May L. (2003) Synthesis, structure characterisation and insecticidal activity of some triorganotin dithiocarbamates. Appl. Organomet. Chem., 17 (4) 218-225; (c) Senkbeil S., Lafleur J. P., Jensen T. G., Kutter J. P. (2012) Gold nanoparticle-based fluorescent sensor for the analysis of dithiocarbamate pesticide in water. Min. System Chem. Life Sci., 1423-1425.
2. (a) Cao S. L., Feng Y. P., Jiang Y. Y., Liu S. Y., Ding G. Y., Li R. T. (2005) Synthesis and in-vitro antitumor activity of 4(3H)-quinazolinone derivatives with dithiocarbamate side chains. Bioorg. Med. Chem. Lett., 15 (7) 1915-1917; (b) Cao S. L., Wang Y., Zhu L., Liao J., Guo Y. W., Chen L. L., Liu H. Q., Xu X. (2010) Synthesis and in-vitro antitumor activity of 4(3H)-quinazolinone derivatives with dithiocarbamate side chains. Eur. J. Med. Chem., 45 (9) 3850-3857; (c) Cao S. L., Han Y., Yuan C. Z., Wang Y., Xiahou Z. K., Liao J., Gao R. T., Mao B. B., Zhao B. L., Li, Z. F., Xu X. (2013) Synthesis and antiproliferative activity of 4-substituted-piperazine-1-carbodithioate derivatives of 2,4-diaminoquinazoline. Eur. J. Med. Chem., 64 401-409; (d) Cvek B., Dvorak Z. (2007) Targeting of nuclear factor-κB and proteasome by dithiocarbamate complexes with metals. Curr. Pharm. Design., 13 (30) 3155-3167; (e) Guzel O., Salman A. (2006) Synthesis, antimycobacterial and antitumor activities of new (1,1-dioxido-3-oxo-1,2-benzisothiazol-2(3H)-yl)methyl N,N-disubstituted dithiocarbamate/O-alkyldithiocarbonate derivatives. Bioorg. Med. Chem., 14 (23) 7804-7815; (f) Qian Y., Ma G. Y., Yang Y., Cheng K., Zheng Q. Z., Mao W. J., Shi L., Zhao J., Zhu H. L. (2010) Synthesis, molecular modeling and biological evaluation of dithiocarbamates as novel antitubulin agents. Bioorg. Med. Chem., 18 (12) 4310-4316.
3. Rudorf W. D. (2007) Reactions of carbon disulfide with N-nucleophiles. J. Sulfur Chem., 28(3) 295-339; (b) Katrizky A. R., Singh S., Mahapatra P. P., Clemense N., Kirichenko K. (2005) Synthesis of functionalised dithiocarbamates via N-(1-benzotriazolylalkyl)dithiocarbamates. .ARKIVOC, IX , 63-79.
4. Greene T. W., Wuts P. G. M. (1999) Protecting Groups in Organic Synthesis 3rd Edition,
5. Gomez L., Wagner A., Mioskowski C. (2000) An efficient procedure for traceless solid-phase synthesis of N,N‘-substituted thioureas by thermolytic cleavage of resin-bound dithiocarbamates. J. Comb. Chem., 2 (1) 75-79.
6. Crich D., Quintero L. (1989) Radical chemistry associated with the thiocarbonyl group. Chem. Rev., 89 (7) 1413-1432.
7. Zhang D., Chen J., Liang Y., Zhou H. (2005) Facile synthesis of novel ionic liquids containing dithiocarbamate. Synth Commun., 35 (4) 521-526.
8. Alexander N., Ramalingam K., Rizzoli C. (2011) Supramolecularly linked linear polymers of thallium(I) dithiocarbamates: Steric influence on the supramolecular interactions of methyl and ethylcyclohexyl dithiocarbamates of thallium(I). Inorg. Chim. Acta. 365 (1) 480-483.
9. (a) Haendel M. A., Tilton F., Bailey G. S., Tanguay R. L. (2004) Developmental toxicity of the dithiocarbamate pesticide sodium metam in Zebrafish. Toxicol. Sci., 81 (2) 390-400; (b) Senkbeil S., Lafleur J. P., Jensen T.G., Kutter J. P. (2012) Gold nanoparticle-based fluorescent sensor for the analysis of dithiocarbamate pesticide in water. Min. System Chem. Life Sci., 1423-1425.
10. Rogachev I., Kampel V., Gusis V., Cohen N., Gressel J., Warshawsky A. (1998) Synthesis, properties and use of copper-chelating amphiphilic dithiocarbamate as synergist of oxidant-generating herbicide. Pesticide Biochem & Physiol., 60 (3) 133-145.
11. Eng G., Song X., Duong Q., Strickman D., Glass J., May L. (2003) Synthesis, structure characterisation and insecticidal activity of some triorganotin dithiocarbamates. Appl. Organomet. Chem., 17 (4) 218-225.
12. Lambert C. (2004) Sulphur chemistry in crop protection. J. Sulphur Chem., 25 (1) 39-62.
13. Byrne S. T., Gu P., Zhou J., Denkin S. M., Chong C., Sullivan D., Liu J. O., Zhang Y. (2007) Pyrrolidine dithiocarbamate and diethyldithiocarbamate are active against growing and nongrowing persister Mycobacterium tuberculosis. Antimicrob. Agents Chemother., 51 (12) 124495-124497.
14. Zheng Y. C., DuanY. C., Ma J. L., Xu R. M., Zi X., Lv W. L.,Wang M. M., Ye X. W., Zhu S., Mobley D., Zhu Y. Y., Wang J. W., Li J. F., Wang Z. R., Zhao W., Liu H. M. (2013) Triazole–dithiocarbamate based selective lysine specific demethylase 1 (LSD1) inactivators inhibit gastric cancer cell growth, invasion, and migration. J. Med. Chem., 56 (21) 8543-8560.
15. Coro J., Atherton R., Little S., Wharton H., Yardley V., Alvarez A., Suarez M., Perez R., Rodriguez H. (2006) Alkyl-linked bis-THTT derivatives as potent in-vitro trypanocidal agents. Bioorg. Med. Chem., 16 (5) 1312-1315.
16. Marakov V., Riabova O. B., Yuschenko A., Urlyapova N., Daudova A., Ziplef P. F., Mollmann U. (2006) Synthesis and antileprosy activity of some dialkyldithiocarbamate. J. Antimicrobial Chemother., 57 (6) 1134-1138.
17. Guzel O., Salman A. (2006) Synthesis, antimycobacterial and antitumor activities of new (1,1-dioxido-3-oxo-1,2-benzisothiazol-2(3H)-yl)methyl N,N-disubstituted dithiocarbamate/ O-alkyldithiocarbonate derivatives. Bioorg Med. Chem., 14 (23) 7804-7815.
18. Zou Y., Yu S., Li R., Zhao Q., Li X., Wu M., Huang T., Chai X., Hu H., Wu Q. (2014) Synthesis, antifungal activities and molecular docking studies of novel 2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl)propyl dithiocarbamates. Eur. J. Med. Chem., 74 366-374.
19. Mohsen U. A. (2014) Synthesis and biological evaluation of some new benzimidazole derivatives bearing dithiocarbamate moiety as potential cholinesterase inhibitors. Cukurova Med. J., 39 (4) 729-735.
20. Jangir S., Bala V., Lal N., Kumar L., Sarswat A., Kumar A., Hamidullah., Saini K. S., Sharma V., Verma V., Maikhuri J. P., Konwar R., Gupta G., Sharma V. L. (2014) Novel alkylphospholipid-DTC hybrids as promising agents against endocrine related cancers acting via modulation of Akt-pathway. Eur. J. Med. Chem., 85 638-647.
21. Chauhan K., Sharma M., Singh P., Kumar V., Shukla P. K., Siddiqi M. I., Chauhan P. M. S. (2012) Discovery of a new class of dithiocarbamates and rhodanine scaffolds as potent antifungal agents: synthesis, biology and molecular docking. Med. Chem. Comm., 3 (9) 1104-1110.
22. Liu P., Li C., Zhang J., Xu X. (2013) Facile and versatile synthesis of alkyl and aryl isothiocyanates by using triphosgene and coolent. Synth. Commun., 43 (24) 3342-3351.
23. Halimjani A. Z., Pourshojaei Y., Saidi M. R. (2009) Highly efficient and catalyst-free synthesis of unsymmetrical thioureas under solvent-free conditions. Tetrahedron Lett. 50 (1) 32-34.
24. Jamir J., Sinha U. B., Nath J., Patel B. K. (2012) Environmentally benign one-pot synthesis of cyanamide from dithiocarbamates using I2 and H2O2. Synth. Commun., 42 (7) 951-958.
25. Kienle M., Unsinn A., Knochel P. (2010) Synthesis of dithiobenzophenes and related class of heterocycles by using functionalized dithiocarbamates. Angew. Chem. Int. Ed., 49 (28) 4751-4754.
26. Aucagne V., Lorin C., Tatibouet A., Rollin P. (2005) Regioselective Michael-induced cyclisation of γ- and δ-hydroxy vinyl sulphides and vinyl dithiocarbamates. Tetrahedron Lett., 46 (25) 4349-4352.
27. Kumar N. K.; Sreeramamurthy, K.; Palle, S.; Mukkanti, K.; Das, P. (2010) Dithiocarbamate and DBU-promoted amide bond formation under microwave condition. Tetrahedron Lett., 51 (6) 899-902.
28. Khalizadeh M. A., Hossaini Z., Baradarani M. A., Hassania A. (2010) A novel isocyanide-based three-component reaction: A facile synthesis of substituted 2H-pyran-3,4-dicarboxylates. Tetrahedron, 66 (43) 8464-8467.
29. Mohsin U. A. (2014) Synthesis and biological evaluation of some new benzimidazole derivatives bearing dithiocarbamate moiety as potential cholinesterase inhibitors. Curkova Med. J., 39 (4) 729-735.
30. Tandel S. K., Rajappa S., Pansare S. V. (1993) Conversion of thiocarbamates to carbamates. Tetrahedron, 49 (34) 7479-7486.
31. Charati F. R., Hossaini Z., Hajinasiri R. (2012) Solvent-free multicomponent reactions of dithiocarbamates, activated acetylenes and isocyanide. J. Applied Chem. Res., 20 (1) 54-59.
32. Bahrin L. J., Jones P. J., Hopf H. (2012) Tricyclic flavonoids with 1,3-dithiolium substructure. Beilstein J. Org. Chem., 8 1999-2003.
33. Burke J. T. R., Bajwa B. S., Jacobsen A. E., Rice K. C., Streaty R. A., Klee W. A. (1984) Probes for narcotic receptor mediated phenomena: Synthesis and pharmacological properties of irreversible ligands specific for .mu. or .delta. opiate receptors. J. Med. Chem., 27 (12) 1570-1574.
34. Walter W., Bode K. D. (1967) Syntheses of Thiocarbamates. Angew. Chem. Int. Ed., 6 (4) 281-293.
35. Garin J., Melandz E., Merchain F. L., Tejero T., Urid S., Ajaysteron J. (1991)Palladium-catalyzed hetero-cope rearrangement of alkyl allyl N-aryldithiocarbonimidates. Synthesis, 147-149.
36. (a) Sharma S. (1978) Thiophosgene in organic synthesis. Synthesis, (11), 803–820; (b) Pascual R. M. (2015) Thiophosgene. Synlett, 26 (12) 1776-1777.
37. (a) Chaturvedi D., Kumar A., Ray S. (2002) An efficient one pot synthesis of carbamates esters through alcoholic tosylates. Synth Commun., 32 (17) 2651-2655; (b) Chaturvedi D., Kumar A., Ray S. (2003) A high yielding, one-pot, novel synthesis of carbamate esters from alcohols using Mitsunobu’s reagent. Tetrahedron Lett., 44 (41) 7637-7639; (c) Chaturvedi D., Ray S. (2005) An efficient, one-pot, basic resin catalyzed novel synthesis of carbamate esters through alcoholic tosylates. Lett. Org. Chem., 2 (8) 742-744; (d) Chaturvedi D., Ray S. (2005) An efficient, basic resin mediated, one-pot synthesis of dithiocarbamate esters through alcoholic tosylates. J Sulfur Chem., 26 (4-5) 365-371; (e) Chaturvedi D., Ray S. (2006) An efficient, basic resin mediated, one-pot synthesis of O-alkyl-S-methyl dithiocarbonates from the corresponding alcohols. J Sulfur Chem., 27 (3) 265-270; (f) Chaturvedi D., Ray S. (2006) An efficient, one-pot, synthesis of dithiocarbamate esters from alcohols using Mitsunobu’s reagent. Tetrahedron Lett., 47 (8) 1307-1309; (g) Chaturvedi D., Mishra N., Mishra V. (2006) Chin. Chem. Lett., 17 (10) 1309-1312; (h) Chaturvedi D., Ray S. (2007) A high yielding one-pot, synthesis of O,S-dialkyl dithiocarbonates from the alcohols using Mitsunobu’s reagent. Tetrahedron Lett., 48 (1) 149-151; (i) Chaturvedi D., Mishra N., Mishra V. (2007) A high yielding, one-pot synthesis of dialkyl carbonates from alcohols using Mitsunobu’s reagent. Tetrahedron Lett., 48 (29) 5043-5045; (j) Chaturvedi D., Mishra N., Mishra V. (2008) An efficient, one-pot synthesis of S-alkyl thiocarbamates from the corresponding thiols using the Mitsunobu reagent. Synthesis, (3) 355-357; (k) Chaturvedi D., Chaturvedi A. K., Mishra N., Mishra V. (2008) An efficient, one-pot synthesis of trithiocarbonates from the corresponding thiols using the Mitsunobu reagent. Tetrahedron Lett., 49 (33) 4886-4888; (l) Chaturvedi D., Chaturvedi A. K., Mishra N., Mishra V. (2009) Basic resin mediated efficient one-pot synthesis of carbazates from the corresponding alkyl halides. J. Iran. Chem. Soc., 6 (3) 510-513; (m) Chaturvedi D., Mishra N., Chaturvedi A. K., Mishra V. (2009)An efficient, basic resin-mediated, one-pot synthesis of dithiocarbazates through alcoholic tosylates. Phosphorus Sulfur and Silicon, 184 (3) 550-558; (n) Chaturvedi A. K., Chaturvedi D., Mishra N., Mishra V. (2010) A high yielding, one-pot synthesis of S,S-dialkyl dithiocarbonates through the corresponding thiols using Mitsunobu’s reagent. J. Iran. Chem. Soc., 7 (3) 702-706; (o) Chaturvedi A. K., Chaturvedi D., Mishra N., Mishra V. (2011)An efficient one-pot synthesis of carbazates and dithiocarbazates through the corresponding alcohols using Mitsunobu’s reagent. J. Iran. Chem. Soc., 8 (2) 396-400; (p) Chaturvedi D., Zaidi S., Chaturvedi A. K., Vaid S., Saxena A. K. (2016) An efficient protocol for the synthesis of β-substituted ethyl dithiocarbamates: A novel class of anti-cancer agent. Ind. J. Chem. Sec. B, 55B (8) 1019-1025.
38. (a) Chaturvedi D., Ray S. (2006) A high yielding, one-pot, triton-B catalyzed, expeditious synthesis of carbamate esters by four component coupling methodology. Monatsh Chem., 137 (2) 201-206; (b) Chaturvedi D., Ray, S. (2006) Triton-B catalyzed efficient one-pot synthesis of dithiocarbamate esters. Monatsh. Chem., 137 (2) 311-317; (c) Chaturvedi D., Ray S. (2006) Triton-B catalyzed, efficient, one-pot synthesis of carbamate esters from alcoholic tosylates. Monatsh. Chem., 137 (4) 459-463; (d) Chaturvedi D., Ray S. (2006) A high yielding, one-pot, triton-B catalyzed synthesis of dithiocarbamates using alcoholic tosylates. Monatsh. Chem., 137 (4) 465-469; (e) Chaturvedi D., Chaturvedi A. K., Mishra N., Mishra V. (2008) Triton-B catalyzed, efficient, one-pot synthesis of carbazates through alcoholic tosylates. Synth. Commun., 38 (22) 4013-4022; (f) Chaturvedi D., Mishra N., Chaturvedi A. K., Mishra V. (2009) Triton-B catalyzed, efficient, one-pot synthesis of dithiocarbazates through alcoholic tosylates. Synth. Commun., 39 (7) 1273-1281.
2. (a) Cao S. L., Feng Y. P., Jiang Y. Y., Liu S. Y., Ding G. Y., Li R. T. (2005) Synthesis and in-vitro antitumor activity of 4(3H)-quinazolinone derivatives with dithiocarbamate side chains. Bioorg. Med. Chem. Lett., 15 (7) 1915-1917; (b) Cao S. L., Wang Y., Zhu L., Liao J., Guo Y. W., Chen L. L., Liu H. Q., Xu X. (2010) Synthesis and in-vitro antitumor activity of 4(3H)-quinazolinone derivatives with dithiocarbamate side chains. Eur. J. Med. Chem., 45 (9) 3850-3857; (c) Cao S. L., Han Y., Yuan C. Z., Wang Y., Xiahou Z. K., Liao J., Gao R. T., Mao B. B., Zhao B. L., Li, Z. F., Xu X. (2013) Synthesis and antiproliferative activity of 4-substituted-piperazine-1-carbodithioate derivatives of 2,4-diaminoquinazoline. Eur. J. Med. Chem., 64 401-409; (d) Cvek B., Dvorak Z. (2007) Targeting of nuclear factor-κB and proteasome by dithiocarbamate complexes with metals. Curr. Pharm. Design., 13 (30) 3155-3167; (e) Guzel O., Salman A. (2006) Synthesis, antimycobacterial and antitumor activities of new (1,1-dioxido-3-oxo-1,2-benzisothiazol-2(3H)-yl)methyl N,N-disubstituted dithiocarbamate/O-alkyldithiocarbonate derivatives. Bioorg. Med. Chem., 14 (23) 7804-7815; (f) Qian Y., Ma G. Y., Yang Y., Cheng K., Zheng Q. Z., Mao W. J., Shi L., Zhao J., Zhu H. L. (2010) Synthesis, molecular modeling and biological evaluation of dithiocarbamates as novel antitubulin agents. Bioorg. Med. Chem., 18 (12) 4310-4316.
3. Rudorf W. D. (2007) Reactions of carbon disulfide with N-nucleophiles. J. Sulfur Chem., 28(3) 295-339; (b) Katrizky A. R., Singh S., Mahapatra P. P., Clemense N., Kirichenko K. (2005) Synthesis of functionalised dithiocarbamates via N-(1-benzotriazolylalkyl)dithiocarbamates. .ARKIVOC, IX , 63-79.
4. Greene T. W., Wuts P. G. M. (1999) Protecting Groups in Organic Synthesis 3rd Edition,
5. Gomez L., Wagner A., Mioskowski C. (2000) An efficient procedure for traceless solid-phase synthesis of N,N‘-substituted thioureas by thermolytic cleavage of resin-bound dithiocarbamates. J. Comb. Chem., 2 (1) 75-79.
6. Crich D., Quintero L. (1989) Radical chemistry associated with the thiocarbonyl group. Chem. Rev., 89 (7) 1413-1432.
7. Zhang D., Chen J., Liang Y., Zhou H. (2005) Facile synthesis of novel ionic liquids containing dithiocarbamate. Synth Commun., 35 (4) 521-526.
8. Alexander N., Ramalingam K., Rizzoli C. (2011) Supramolecularly linked linear polymers of thallium(I) dithiocarbamates: Steric influence on the supramolecular interactions of methyl and ethylcyclohexyl dithiocarbamates of thallium(I). Inorg. Chim. Acta. 365 (1) 480-483.
9. (a) Haendel M. A., Tilton F., Bailey G. S., Tanguay R. L. (2004) Developmental toxicity of the dithiocarbamate pesticide sodium metam in Zebrafish. Toxicol. Sci., 81 (2) 390-400; (b) Senkbeil S., Lafleur J. P., Jensen T.G., Kutter J. P. (2012) Gold nanoparticle-based fluorescent sensor for the analysis of dithiocarbamate pesticide in water. Min. System Chem. Life Sci., 1423-1425.
10. Rogachev I., Kampel V., Gusis V., Cohen N., Gressel J., Warshawsky A. (1998) Synthesis, properties and use of copper-chelating amphiphilic dithiocarbamate as synergist of oxidant-generating herbicide. Pesticide Biochem & Physiol., 60 (3) 133-145.
11. Eng G., Song X., Duong Q., Strickman D., Glass J., May L. (2003) Synthesis, structure characterisation and insecticidal activity of some triorganotin dithiocarbamates. Appl. Organomet. Chem., 17 (4) 218-225.
12. Lambert C. (2004) Sulphur chemistry in crop protection. J. Sulphur Chem., 25 (1) 39-62.
13. Byrne S. T., Gu P., Zhou J., Denkin S. M., Chong C., Sullivan D., Liu J. O., Zhang Y. (2007) Pyrrolidine dithiocarbamate and diethyldithiocarbamate are active against growing and nongrowing persister Mycobacterium tuberculosis. Antimicrob. Agents Chemother., 51 (12) 124495-124497.
14. Zheng Y. C., DuanY. C., Ma J. L., Xu R. M., Zi X., Lv W. L.,Wang M. M., Ye X. W., Zhu S., Mobley D., Zhu Y. Y., Wang J. W., Li J. F., Wang Z. R., Zhao W., Liu H. M. (2013) Triazole–dithiocarbamate based selective lysine specific demethylase 1 (LSD1) inactivators inhibit gastric cancer cell growth, invasion, and migration. J. Med. Chem., 56 (21) 8543-8560.
15. Coro J., Atherton R., Little S., Wharton H., Yardley V., Alvarez A., Suarez M., Perez R., Rodriguez H. (2006) Alkyl-linked bis-THTT derivatives as potent in-vitro trypanocidal agents. Bioorg. Med. Chem., 16 (5) 1312-1315.
16. Marakov V., Riabova O. B., Yuschenko A., Urlyapova N., Daudova A., Ziplef P. F., Mollmann U. (2006) Synthesis and antileprosy activity of some dialkyldithiocarbamate. J. Antimicrobial Chemother., 57 (6) 1134-1138.
17. Guzel O., Salman A. (2006) Synthesis, antimycobacterial and antitumor activities of new (1,1-dioxido-3-oxo-1,2-benzisothiazol-2(3H)-yl)methyl N,N-disubstituted dithiocarbamate/ O-alkyldithiocarbonate derivatives. Bioorg Med. Chem., 14 (23) 7804-7815.
18. Zou Y., Yu S., Li R., Zhao Q., Li X., Wu M., Huang T., Chai X., Hu H., Wu Q. (2014) Synthesis, antifungal activities and molecular docking studies of novel 2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl)propyl dithiocarbamates. Eur. J. Med. Chem., 74 366-374.
19. Mohsen U. A. (2014) Synthesis and biological evaluation of some new benzimidazole derivatives bearing dithiocarbamate moiety as potential cholinesterase inhibitors. Cukurova Med. J., 39 (4) 729-735.
20. Jangir S., Bala V., Lal N., Kumar L., Sarswat A., Kumar A., Hamidullah., Saini K. S., Sharma V., Verma V., Maikhuri J. P., Konwar R., Gupta G., Sharma V. L. (2014) Novel alkylphospholipid-DTC hybrids as promising agents against endocrine related cancers acting via modulation of Akt-pathway. Eur. J. Med. Chem., 85 638-647.
21. Chauhan K., Sharma M., Singh P., Kumar V., Shukla P. K., Siddiqi M. I., Chauhan P. M. S. (2012) Discovery of a new class of dithiocarbamates and rhodanine scaffolds as potent antifungal agents: synthesis, biology and molecular docking. Med. Chem. Comm., 3 (9) 1104-1110.
22. Liu P., Li C., Zhang J., Xu X. (2013) Facile and versatile synthesis of alkyl and aryl isothiocyanates by using triphosgene and coolent. Synth. Commun., 43 (24) 3342-3351.
23. Halimjani A. Z., Pourshojaei Y., Saidi M. R. (2009) Highly efficient and catalyst-free synthesis of unsymmetrical thioureas under solvent-free conditions. Tetrahedron Lett. 50 (1) 32-34.
24. Jamir J., Sinha U. B., Nath J., Patel B. K. (2012) Environmentally benign one-pot synthesis of cyanamide from dithiocarbamates using I2 and H2O2. Synth. Commun., 42 (7) 951-958.
25. Kienle M., Unsinn A., Knochel P. (2010) Synthesis of dithiobenzophenes and related class of heterocycles by using functionalized dithiocarbamates. Angew. Chem. Int. Ed., 49 (28) 4751-4754.
26. Aucagne V., Lorin C., Tatibouet A., Rollin P. (2005) Regioselective Michael-induced cyclisation of γ- and δ-hydroxy vinyl sulphides and vinyl dithiocarbamates. Tetrahedron Lett., 46 (25) 4349-4352.
27. Kumar N. K.; Sreeramamurthy, K.; Palle, S.; Mukkanti, K.; Das, P. (2010) Dithiocarbamate and DBU-promoted amide bond formation under microwave condition. Tetrahedron Lett., 51 (6) 899-902.
28. Khalizadeh M. A., Hossaini Z., Baradarani M. A., Hassania A. (2010) A novel isocyanide-based three-component reaction: A facile synthesis of substituted 2H-pyran-3,4-dicarboxylates. Tetrahedron, 66 (43) 8464-8467.
29. Mohsin U. A. (2014) Synthesis and biological evaluation of some new benzimidazole derivatives bearing dithiocarbamate moiety as potential cholinesterase inhibitors. Curkova Med. J., 39 (4) 729-735.
30. Tandel S. K., Rajappa S., Pansare S. V. (1993) Conversion of thiocarbamates to carbamates. Tetrahedron, 49 (34) 7479-7486.
31. Charati F. R., Hossaini Z., Hajinasiri R. (2012) Solvent-free multicomponent reactions of dithiocarbamates, activated acetylenes and isocyanide. J. Applied Chem. Res., 20 (1) 54-59.
32. Bahrin L. J., Jones P. J., Hopf H. (2012) Tricyclic flavonoids with 1,3-dithiolium substructure. Beilstein J. Org. Chem., 8 1999-2003.
33. Burke J. T. R., Bajwa B. S., Jacobsen A. E., Rice K. C., Streaty R. A., Klee W. A. (1984) Probes for narcotic receptor mediated phenomena: Synthesis and pharmacological properties of irreversible ligands specific for .mu. or .delta. opiate receptors. J. Med. Chem., 27 (12) 1570-1574.
34. Walter W., Bode K. D. (1967) Syntheses of Thiocarbamates. Angew. Chem. Int. Ed., 6 (4) 281-293.
35. Garin J., Melandz E., Merchain F. L., Tejero T., Urid S., Ajaysteron J. (1991)Palladium-catalyzed hetero-cope rearrangement of alkyl allyl N-aryldithiocarbonimidates. Synthesis, 147-149.
36. (a) Sharma S. (1978) Thiophosgene in organic synthesis. Synthesis, (11), 803–820; (b) Pascual R. M. (2015) Thiophosgene. Synlett, 26 (12) 1776-1777.
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