10
G. AZADI ET AL.
References
[1] Herradura PS, Pendola KA, Guy RK. Copper-mediated cross-coupling of aryl boronic acids
and alkyl thiols. Org Lett. 2000;2:2019–2022.
[2] Gangjee A, Zeng Y, Talreja T, et al. Design and synthesis of classical and nonclassi-
cal 6-arylthio-2,4-diamino-5-ethylpyrrolo[2,3-d]pyrimidines as antifolates. J Med Chem.
[3] Takimiya K, Shinamura S, Osaka I, et al. Thienoacene-based organic semiconductors. Adv
Mater. 2011;23:4347–4370.
[4] Okamoto T, Mitsui C, Yamagishi M, et al. V-shaped organic semiconductors with solution
processability, high mobility, and high thermal durability. Adv Mater. 2013;25:6392–6397.
[5] Mori T, Nishimura T, Yamamoto T, et al. Consecutive thiophene-annulation approach to π-
extended thienoacene-based organic semiconductors with [1]benzothieno[3,2-b][1]benzothi-
[6] Soleiman-Beigi M, Mohammadi F. A novel nickel-catalyzed domino method for the direct
synthesis of symmetrical disulfides using potassium 5-methyl-1,3,4-oxadiazole-2-thiolate as
a sulfurating reagent. Synlett. 2015;26:911–914.
[7] Ghorbani-Choghamarani A, Taherinia Z. Synthesis of peptide nanofibers decorated with
palladium nanoparticles and its application as an efficient catalyst for the synthesis of
sulfides via reaction of aryl halides with thiourea or 2-mercaptobenzothiazole. RSC Adv.
[8] Ley SV, Thomas AW. Modern synthetic methods for copper-mediated C(aryl)–O, C(aryl)–N,
and C(aryl)–S bond formation. Angew Chem Int Ed. 2003;42:5400–5449.
[9] Taniguchi N, Onami T. Magnesium-induced copper-catalyzed synthesis of unsymmetrical
diaryl chalcogenide compounds from aryl iodide via cleavage of the Se–Se or S–S bond. J Org
[10] Taniguchi N. Alkyl- or arylthiolation of aryl iodide via cleavage of the S–S bond of disulfide
compound by nickel catalyst and zinc. J Org Chem. 2004;69:6904–6906.
[11] Mondal J, Borah P, Modak A, et al. Cu-grafted functionalized mesoporous SBA-15: a novel
heterogeneous catalyst for facile one-pot three-component C–S cross-coupling reaction of aryl
halides in water. Org Process Res Dev. 2014;18:257–265.
[12] Firouzabadi H, Iranpoor N, Gholinejad M. One-pot thioetherification of aryl halides using
thiourea and alkyl bromides catalyzed by copper(I) iodide free from foul-smelling thiols in
[13] Chai Y, Dong D, Ouyang Y, et al. Thia-Michael addition reactions in water using 3-
[Bis(alkylthio) methylene] pentane-2,4-diones as odorless and efficient thiol equivalents. Lett
Org Chem. 2007;4:281–284.
[14] Bartolozzi A, Foudoulakis HM, Cole BM. Development of a tandem base-catalyzed,
triphenylphosphine-mediated disulfide reduction-Michael addition. Synthesis. 2008;2008:
2023–2032.
[15] Dong DW, Yu HF, Ouyang Y, et al. Thia-Michael addition reactions using 2-[Bis(alkylthio)
methylene]-3-oxo-N-o-tolylbutanamides as odorless and efficient thiol equivalents. Synlett.
2006;2:283–287.
[16] Niu LF, Cai Y, Liang C, et al. Efficient copper-catalyzed C–S cross-coupling of heterocyclic
thiols with aryl iodides. Tetrahedron. 2011;67:2878–2881.
[17] Zhou WX, Yin B, Li J, et al. A C–S cross-coupling observed in situ reaction of 2-
mercaptobenzothiazole with CuI. Inorg Chim Acta. 2013;408:209–213.
[18] Yang D, Yan K, Wei W, et al. Metal-free iodine-catalyzed direct arylthiation of substituted
anilines with thiols. J Org Chem. 2015;80:6083–6092.
[19] Yan K, Yang D, Sun P, et al. Direct thiolation of methoxybenzenes with thiols under metal-free
conditions by iodine catalysis. Tetrahedron Lett. 2015;56:4792–4795.
[20] Yang D, Sun P, Wei W, et al. Metal-free iodine-catalyzed direct cross-dehydrogenative coupling
(CDC) between pyrazoles and thiols. Org Chem Front. 2016;3:1457–1461.