Facile access to libraries of diversely substituted 2-aryl-benzoxazoles/benzothiazoles from readily accessible aldimines via cyclization/cross coupling in imidazolium-ILs with Pd(OAc)2 or NiCl2 (dppp) as catalyst

[1]  K. Laali,et al.  1-Aryltriazenes in the Suzuki, Heck, and Sonogashira Reactions in Imidazolium-ILs, with [BMIM(SO3H)][OTf] or Sc(OTf)3as Promoter, and Pd(OAc)2or NiCl2·glyme as Catalyst , 2019, European Journal of Organic Chemistry.

[2]  K. Laali,et al.  Facile Access to Diverse Libraries of Internal Alkynes via Sequential Iododediazoniation/Decarboxylative Sonogashira Reaction in Imidazolium ILs without Ligand or Additive , 2019, European Journal of Organic Chemistry.

[3]  K. Laali,et al.  Libraries of C-5 Substituted Imidazoles and Oxazoles by Sequential Van Leusen (VL)-Suzuki, VL-Heck and VL-Sonogashira in Imidazolium-ILs with Piperidine-Appended-IL as Base , 2018, European Journal of Organic Chemistry.

[4]  A. Biffis,et al.  Pd Metal Catalysts for Cross-Couplings and Related Reactions in the 21st Century: A Critical Review. , 2018, Chemical reviews.

[5]  H. Deng,et al.  Copper-Catalyzed Arylation of Benzothiazoles with Toluene Derivatives: Synthesis of 2-Arylbenzothiazole , 2017, Synthesis.

[6]  Rui Wang,et al.  Pd‐Catalyzed C−H Arylation of Benzothiazoles with Diaryliodonium Salt: One‐Pot Synthesis of 2‐Arylbenzothiazoles , 2017 .

[7]  K. Laali,et al.  [bmim(SO3H)][OTf]/[bmim][X] and Zn(NTf2)2/[bmim][X] (X = PF6 and BF4); efficient catalytic systems for the synthesis of tetrahydropyrimidin-ones (-thiones) via the Biginelli reaction , 2016 .

[8]  K. Ramesh,et al.  Direct C–H arylation of benzothiazoles by magnetically separable nano copper ferrite, a recyclable catalyst , 2015 .

[9]  Gao‐Nan Li,et al.  Highly phosphorescent iridium(III) complexes based on 2-(biphenyl-4-yl)benzo[d]oxazole derivatives: synthesis, structures, properties and DFT calculations , 2015 .

[10]  Fu‐She Han Transition-metal-catalyzed Suzuki-Miyaura cross-coupling reactions: a remarkable advance from palladium to nickel catalysts. , 2013, Chemical Society reviews.

[11]  K. Laali,et al.  Schmidt reaction in ionic liquids: highly efficient and selective conversion of aromatic and heteroaromatic aldehydes to nitriles with [BMIM(SO3H)][OTf] as catalyst and [BMIM][PF6] as solvent , 2013 .

[12]  K. Laali,et al.  Pd(OAc)2 catalyzed synthesis of 2-aryl- and 2-heteroaryl-benzoxazoles and benzothiazoles in imidazolium ionic liquids (ILs) without additives and with recycling/reuse of the IL , 2012 .

[13]  K. Laali,et al.  Highly efficient synthesis of amides via Ritter chemistry with ionic liquids , 2011 .

[14]  Xiaogang Liu,et al.  Direct arylation of benzothiazoles and benzoxazoles with aryl boronic acids. , 2011, Chemistry.

[15]  G. Loudos,et al.  Evaluation of Re and (99m)Tc complexes of 2-(4'-aminophenyl)benzothiazole as potential breast cancer radiopharmaceuticals. , 2010, Journal of medicinal chemistry.

[16]  A. Kozikowski,et al.  In pursuit of natural product leads: synthesis and biological evaluation of 2-[3-hydroxy-2-[(3-hydroxypyridine-2-carbonyl)amino]phenyl]benzoxazole-4-carboxylic acid (A-33853) and its analogues: discovery of N-(2-benzoxazol-2-ylphenyl)benzamides as novel antileishmanial chemotypes. , 2008, Journal of medicinal chemistry.

[17]  E. Stone,et al.  Synthesis and biological properties of benzothiazole, benzoxazole, and chromen-4-one analogues of the potent antitumor agent 2-(3,4-dimethoxyphenyl)-5-fluorobenzothiazole (PMX 610, NSC 721648). , 2008, Journal of medicinal chemistry.

[18]  J. Ellman,et al.  Arylation of heterocycles via rhodium-catalyzed C-H bond functionalization. , 2004, Organic letters.

[19]  Akira Suzuki,et al.  Recent advances in the cross-coupling reactions of organoboron derivatives with organic electrophiles, 1995–1998 , 1999 .

[20]  E. Stone,et al.  Antitumor benzothiazoles. 26.(1) 2-(3,4-dimethoxyphenyl)-5-fluorobenzothiazole (GW 610, NSC 721648), a simple fluorinated 2-arylbenzothiazole, shows potent and selective inhibitory activity against lung, colon, and breast cancer cell lines. , 2006, Journal of medicinal chemistry.