“…Iron(III) dimer complex, [31] Modified Vilsmeier-Haack reagents TCCA/DMF, TCTA/DMF (SOCl 2 /DMF, POCl 3 /DMF), [32] FeÀ Mn cyanide, [33] Stefan et. al., reported the boronic acid synthesis via monophasic transesterification by evaporation of reagents/ byproducts, [34] Zn-PAM, [35] MCS, [36] ultrasonic technique, [37] DBU-CO 2 , [38] enzymatic transesterification, [39] M 2 CO 3 or MI (M = Li, Na, K, Cs), [40] pPh-SO 3 H & pBPA-SO 3 H, [41] Ti(Oi-pr) 4 , [42] NaOR, [43] Metal/ ETS-10, [44] BBAIL, [45] EmimOAc, [46] BF 3 .OEt 2 , [47] Zn(Me) 2 , [48] N-Heterocyclic olefins, [49] microwave irradiation, [50] dilithium tetra-tertbutylzincate, [51] K 2 CO 3 /DMSO, [52] Ionic liquid (references therein), [53] methylboronic acid, [54] AuÀ Cu nanoparticles, [55] CO 2 / Novozym-435, [56] CuFe 2 O 4 , [57] Cesium carbonate, [58] Ion-exchange resins (Lewatit K1221), [59] imidazolium ionic liquids, [60] 4-(3methyl-1-imidazolio)-1-butanesulfonic acid triflate, [61] Mn(II) Carbonate & Mn(II)Sulfate, [62] DBU at high pressure, [63] ball-mill technique, [64] AgOTf, [65] Sol-Gel MoO 3 /TiO 2 , [66] lipase from Aspergillus niger, [67] TEA, [68] Sn-catalyst, [69] lanthanum(III) Isopropoxide, [70] Candida rugo...…”