۹- Shahrisa, A.; Esmati, S.; Gh. N., M.; Boric acid as a mild and efficient catalyst for one- pot synthesis of 1-amidoalkyl-2-naphthols under solvent- free condhtions.(2012), Chemical Science, 124, 927- 931.
۱۰- Wender, P. A.; Handy, S.; Wright, D. L.; Towards the ideal synthesis. , (۱۹۹۷),۱۹, ۷۶۵-۷۷۴.
۱۱- (a) Ramazani, A.; Rezaei, A.; Novel one-pot, four-component condensation reaction: an efficient approach for the synthesis of 2,5-disubstituted 1,3,4-oxadiazole derivatives by a ugi-4CR/aza-wittig sequence. (۲۰۱۰), , ۱۲, ۲۸۵۲-۲۸۵۵.
۱۲- Santra, S.; Andreana, P. R.; A One-Pot, Microwave-Influenced synthesis of diverse small molecules by multicomponent reaction cascades. (۲۰۰۷), Organic Letters, 9, 5035-5038.
۱۳- Kolb, J.; Beck, B.;Domling ,A.; Simultaneous assembly of the-lactam and thiazole moiety by a new multicomponent reaction. (۲۰۰۲), Tetrahedron Letters,43, 6901.
۱۴- Oae, S., Organic Sulfur Chemistry: Structure and Mechanism, CRC: Boca Raton, FL, ۱۹۹۱.
۱۵- Metzner P, Thuillier A., reagents in organic synthesis, Katritzky AR, Meth-Cohn O, Rees CW Sulfur Academic, San Diego, ۱۹۹۴.
۱۶- Pe’er, I. C.; Felder, E.; Man, O.; Silman, I.; Sussman, J. L.; Proteomic signatures: Amino acid and oligopeptide compositions differentiate among phyla.(2004), Proteins: Structure, Function, and Bioinformatics, ۵۴, ۲۰.
۱۷- Bardwell, J. C.; Building bridges: disulphide bond formation in the cell. (1994) , , ۱۴, ۱۹۹.
۱۸- M. Heravi, M.; Derikvand, F.; A.Oskooie, H.; Silica-supported bis(tri methyl silyl) chromate: oxidation of thiols to their correspouding disulfides. (2007), synthetic communications, 37, 513-517.
۱۹- W.Kabalka, G.; Serinivasa Reddy, M.; Yao, M.L.; Synthesis of diaryl disulfidesvia the reductive coupling of aryl sulfonyl chlorides. (2009), Tetrahedron Letters, 50, 7340-7342.
۲۰- Hekmatshoar, N.; Sajdi, S.; Heravi, M.; Bamoharram, F.; H14[NaP5W30O110] as a heterogeneous recyclable catalyst for the air oxidation of thiols under solvent free conditions. (2007), Molecules, ۱۲, ۲۲۲۳-۲۲۲۸.
۲۱- Bioschoff, L.; David, C.; Martin, L.; Meudal, H.; Roques, B.-P.; Fournie- Zaulski; M.-C. 2,4-Dinitrophenyl 4-methoxybenzyl disulfide: A new efficient reagent for the electrophilic sulfenylation of b-amino ester enolates. (1997), , ۶۲, ۴۸۴۸.
۲۲- Turow, S.; Pereira, V.A .; Martinez, D.M.; Alves, D.; Jacob, R.G.; Lenardao, E.J.; Base-free oxidation of thiols to disulfides using selenium ionic liquid. (2011), Tetrahedron Leters, 52, 640-643.
۲۳- Gul, K.; Narajana Perumel, S.; Dornelles, L.; Rodrigues, O.E.D., Bimetallic system for the synthesis of diorganyl selenides and sulfides, chiral b-seleno amines and seleno and thioesters. (2011), Tetrahedron Letters, 52, 3592-3596.
۲۴- Cruz, I.; Cruz, M.E.; Carrasco, F.; Horton, J.; Neurocysticercosis: optimal dose treatment with albendazole.(1995), Journal of the Neurological Sciences, 133, 152–۱۵۴.
۲۵- (a) Jortani, S.A.; Valentour, J.C.; Poklis, A.; Thioridazine enantiomers in human tissues.(1994), Forensic Science International, 64, 165–۱۷۰. (b) Rho, S.B.; Kim, B.R.; Kang, S.; A gene signature-based approach identifies thioridazine as an inhibitor of phosphatidylinositol-3′-kinase (PI3K)/AKT pathway in ovarian cancer cells.( ۲۰۱۱), Gynecologic Oncology, ۱۲۰,. ۱۲۱–۱۲۷.
۲۶- (a) Shaabani, A.; Rezayan, A. H.; Silica sulfuric acid promoted selective oxidation of sulfides to sulfoxides or sulfones in the presence of aqueous H2O2.(2007), , ۸, ۱۱۱۲-۱۱۱۶. (b) Huang, Y. B.; Yi, W. B.; Cai, C.; A recyclable fluorous thiourea organocatalyst for the chemoselective oxidation of sulfides. (2011), J. Fluor. Chem, 132, 554–۵۵۷. © Bahrami, K.; Khodaei, M. M.; Soheilizad, M.; Direct conversion of thiols and disulfides into sulfonamides.(2010), Tetrahedron Letters, 51, 4843–۴۸۴۶.
۲۷- Munbunjong, W.; Lee, E.H.; Ngernmaneerat, P.; Kim, S.J.; Singh, G.; Chavasiri, W.; Jang, D.O.; Indium-mediated cleavage of diphenyl diselenide and diphenyl disulfide: efficient one-pot synthesis of unsymmetrical diorganyl selenides, sulfides and selenoesters. (2009), Tetrahedron Letters, 65, 2467-2471.
۲۸- Nishiyama, Y.; Maehira, K.; Nakase, J .; Sonoda, N.; A new method for synthesis of s-aryl-o-alkyl thiolcarbonates: selenium-catalyzed reaction of alcohols with carbon monoxide and diaryl disulfides. (2005) , Tetrahedron Letters, 46,7415-7417.
۲۹- Alves, D.; G.Lara, R.; Contreira, M.; S.Radatz, C.;F.B. Duarte,L.; Perin, G.; Copper-catalyzed sulfenylation of pyrroles with disulfide or thio: directly synthesis of sulfuenylation of pyrrols , sulfenyle pyrroles. (2012), Tetrahedron Letters, 53,3364.
۳۰- Banerjee, S.; Adak, L.; C.Ranu,B.; Ionic liqud/pph3 promotedcleavage of diphenyl disulfide and diselenide: a straight-forward metal-free one-pot route to the synthesis of unsymmetrical sulfides and selenides. (2012), Tetrahedron Letters, 53, 2149-2152.
۳۱- Hekmatshoar, R.; Sajadi, S.; Heravi, M. M.; Bamoharram, F.; H14[NaP5W30O110] as a Heterogeneous Recyclable Catalyst for the Air Oxidation of Thiols Under Solvent Free Conditions. (2007), Molecules, 12, 2223.
۳۲- a) Zolfigol, M. A.; Silica sulfuric acide/ NaNO2 as a novel hetrogenous system for production of thionitrite and disulfides under mild condation. (2001), Tetrahedron Letters, 57, 9509. b) Ghorbani-Choghamarani, A.; Nikoorazm, M.; Godarziafshar, H. ; Shokr, A.; Almasi, H.; Metal- free oxidative coupling of thiols to disulfide using guanidinium nitrae or nitro urea in the presence of silica acide sulfur acide. (2011), , ۱۲۳, ۴۵۳.
۳۳- M. Heravi, M.; Derikvand, F.; A.Oskooie, H.; Silica-supported bis(tri methyl silyl) chromate: oxidation of thiols to their correspouding disulfides. (2007), synthetic communications, 37, 513-517.
۳۴- Karami, B.;Montazerozohori, M.; Habibi, M.H.; Urea- Hydrogen Peroxide (UHP) Oxidation of thiols to the corresponding disulfides promoted by malic anhydride as mediator. (2005), Molecules, 10, 1358.
۳۵- Chaturvedi, D.; Mishra, N.; Chaturvedi, A. K.; Mishra, V.; An efficient, one pot synthesis of Trithiocarbonates from alcoholic tosylates using the CsCO3/CS2 system. (2008), Monatshefte für Chemie -Chemical Monthly ,139, 1467-1470.
۳۶- Soleiman-Beigi, M.; Izadi, A.; CuI-Catalyzed: One-Pot Synthesis of Diaryl Disulfides from Aryl Halides and Carbon Disulfide. (2013), Journal of Chemistry, ۲۰۱۳, ۱-۵.
۳۷- Chaturvedi, D.; Chaturvedi, A.K.; Mishra, N.;Mishra, V.; An efficient, one-pot synthesis of trithiocarbonates from the correaponding thiols using the Misunobu reagent. (2008), Tetrahedron Letters, 49,4886.
۳۸- Samuel, R.; Asokan,C.V.; Suma, S.; Chandran, P.; Retnamma, S.; Anabha, R.E; Afacile method for the synthesis of substituted 2-ylidene – ۱,۳- oxathioles from acetophenoles. (2007), Tetrahedron Letters, 48, 8376.
۳۹-Devi,N.S.; Sing, S.J.;Sing, O.M; An Efficient One-pot Multicomponet Synthesis of 2,3- Dihedro-3-alkyl/aryl 2- thioxoquinazoline-4(H)- Ones under, Solvent – Free condations. (2012), Synlett, 23, 2111.
۴۰- Rzayev, Z.O.; Turk,M.; Sylemez, E.A; Bioengineering functional coplymers. XXl. Synthesis of novel and carboxyl- trithiocarbonate functionalized poly (malic anhydride) and its interaction with cancer cells. (2012), Bioorganic & Medicinal Chemistry Letters, 20, 5053.
۴۱- Carta,F.; Akdemir.; Scozzafava, A.; Masini, E.; Supuran, C; Xanthes and trithiocarbonates Inhibit Carbonic Anhydrase and Show Antiglaucoma Effects in Vivo. (2013), Journal of Medicinal Chemistry, 56, 4691.
۴۲ - Tomita, K.; Nagano, M. Sankyo Co., Ltd.: Japan, ; ۴ pp, ۱۹۶۸.
۴۳- Daum, S. J. Sterling Drug Inc.: USA, united states patent application publication.; 2 pp, ۱۹۷۸.
۴۴- Renner, H. J.; Schneider, G.; Weissflog, J.; “East Ger. Patent 15,431 (1958)." Chemical abstracts. 54. ۱۹۶۰.
۴۵- Daoben, H.; Controlled Free- Radical polymerization of Methy Acrylate in the presence of a Cyclic Trithiocarbonate under- Ray Irradiation at Low Temperature. (2007), European Polymer Journal, 43,847.
۴۶- (a) Reid, E. E.; Organic chemistry of bivalent sulfur. (1966), Chem. Publ. co. In. C., NewYork, 1-6,1958 (b) Hosseini, H.; Javadi,, M.; Moghiman,, M.; Ghodsi Rad, M. H.; Carbon Disulfide Production via Hydrogen Sulfide Methane Reformation. (2010), Engineering and Technology, 62, 628-631.
۴۷- Ramadas, S.R.; Srinivasan, P.S.; Ramachandran, J.; Sastry, V. V. S. K.; Methods of synthesis of dithiocarboxylic acids and esters. (1983), Synthesis, 8, 605.
۴۸- (a) Foster, A. B.; Wolfrom, M. L.; An Anomalous Reaction of Methyl 3,4-O-Isopropylidene-β-D-arabinopyranoside 2-O-(S-Sodium Dithiocarbonate) . (1965) , Journal of The American Chemical Society, 78, 2493 (b) Mashhood, A. S.; Tanimoto, S. J.; Reaction of lithium enolates with carbon disulfide: synthesis of O-(1-alkoxy-2,2-dialkylvinyl) S-alkyl dithiocarbonates. (1989) , The Journal of Organic Chemistry, 54, 5603-5607.
۴۹- Godt, H. C.; Wann, R. E.; The synthesis of organic trithiocarbonates. (1961) , The Journal of Organic Chemistry, 26, 4047-4051.
۵۰- (a) Ranu, B. C.; Dey, S. S.; Bag, S.; A simple and green procedure for the synthesis of symmetrical N,N’ -disubstituted thioureas on the surface of alumina under microwave irradiation. (2003), Arkat USA, Inc, ix,14-20. (b) Ballabeni, M.; Ballini, R.; Bigi, F.; Maggi, R.; Parrini, M.; Predieri, G.; Sartori, G.; Synthesis of Symmetrical N, N’-Disubstituted Thioureas and Heterocyclic Thiones from Amines and CS2 over a ZnO/Al2O3 Composite as Heterogeneous and Reusable Catalyst. (1999), The Journal of Organic Chemistry, 64, 1029-1032.
۵۱- Sahoo, B. M.; B. V. V. , R. K.; Kumari, P.; Synthesis, characterization and biological evaluation of novel oxadiazole derivatives. (2011), International Journal of Pharmaceutical Sciences Review and Research, 2, 344-350.
۵۲- Jha, K. K.; Samad, A.; Kumar, Y.; Shaharyar, M.; Khosa, R. L.; Jain, J.; Kumar, V.; Singh, P.; Design, synthesis and biological evaluation of 1,3,4-oxadiazole derivatives. (2010), , ۴۵, ۴۹۶۳-۴۹۶۷.
۵۳- West, R.; Astel, M .; Physical constant s of organic compounds. (1979), Hand book of chemistry and physics, 46, 540.
۵۴- Govers, H.; Rueper, C.; Stevens, T.; Leeuwen,V.; Exper imental determination and prediction of partition coefficients of thioureas and their toxicity to photobacterium phosphoreum. (1986), Chemospader, ۱۵, ۳۸۳-۳۹۳.
۵۵- Martschenk, B.; Beck, F.; Bauer, W.; Thiourea derivates. (1955), Ulmanns encyclopedia of industrial chemistry, 26, 803-815.
۵۶- Clark. J.H ; Fluoride Ion as a Base in Organic Synthesis. (1980), Chemical Reviews, ۸۰, ۴۲۹-۴۵۲.
۵۷- O¨ stlund, Å; Lundberg ,D.; Nordstierna ,L; Holmberg, K; Nyde, M; Dissolution and Gelation of Cellulose in TBAF/DMSO Solutions:The Roles of Fluoride Ions and Water .(2009), Biomacromolecules,10, 2401–۲۴۰۷.
۵۸- (a) Corey, E. J.; Snider, B. B. Journal of The American Chemical Society (۱۹۷۲), ۹۴, ۲۵۴۹-۲۵۵۰
۵۹- Sonavane,S.U.; Chidambaram, M.; Almog, J.; Sasson, Y; Rapid and efficient synthesis of symmetrical alkyl disulfides Under ohase transfer condations.(2007) , Tetrahedron Letters, 48, 6048.
۶۰- Firouzabadi, H; Iranpoor, N; Abbasi, M; A one-pot, efficient, and odorless synthesis of symmetrical disulfides using organic halides and thiourea in the presence of manganese dioxide and wet polyethylene glycol (PEG-200). (2010) , Tetrahedron Letters , ۵۱ , ۵۰۸–۵۰۹.
۶۱- Soleiman-Beigi, M.; Mohammadi, F. A novel copper-catalyzed, one-pot synthesis of symmetric organic disulfides from alkyl and aryl halides: potassium 5-methyl-1,3,4-oxadiazole-2-thiolate as a novel sulfur transfer reagent; (2012) , Tetrahedron Letters , ۵۳, ۷۰۲۸-۷۰۳۰.
۶۲- Soleiman-Beigi, M.; Hemmati, M.; An efficient, one-pot and CuCl-catalyzed route to the synthesis of symmetric organic disulfides via domino reactions of thioacetamide and aryl (alkyl) halides. (2013) , , ۲۷, ۷۳۴–۷۳۶.
۶۳-Tajbakhsh, M.; Hosseinzadeh, R.; Shakoori,A.; 2,6- Dicarboxy pyridinium chlorochromate:an efficient and Selective reag for the oxidation of thiols to disulfides to sulfoxides. (2004), Tetrahedron Letters, 45,1889.
۶۴- Vandavasi, J.K.; Hu, W.P.; Chen, C.Y.; Wang, J.J.; Efficient synthesis of unsymmetrical disulfides .(2011), Tetrahedron Letters, 8895–۸۹۰۱.
۶۵- Christoforous,A.; Nicolaou , G.; Elems,Y; N-Phenyltriazoline as an efficient, Selective, and reusale Reagent for the oxidation of thiols to disulfides.(2006), Tetrahedron Letters, ۴۷, ۹۲۱۱.
