Results 81 to 90 of about 7,247 (206)

A copper bromide-decorated magnetic oyster shell biosupport as a sustainable catalyst for heterogeneous synthesis of imidazo[1,2-<i>a</i>]pyridines in glycerol. [PDF]

Nanoscale Adv
Ansari S, Salamatmanesh A, Miraki MK, Heydari A.   +3 more
europepmc   +1 more source

C₃-Alkylation of Imidazo[1,2-a]pyridines via Three-Component Aza-Friedel-Crafts Reaction Catalyzed by Y(OTf)₃. [PDF]

Molecules
Yang K, Chen CB, Liu ZW, Li ZL, Zeng Y, Wang ZY.   +5 more
europepmc   +1 more source

Catalyst free, C-3 functionalization of imidazo[1,2-a]pyridines to rapidly access new chemical space for drug discovery efforts. [PDF]

Chem Commun (Camb), 2018
Gunaganti N, Kharbanda A, Lakkaniga NR, Zhang L, Cooper R, Li HY, Frett B.   +6 more
europepmc   +1 more source

Atroposelective synthesis of axially chiral imidazo[1,2-a]pyridines via asymmetric multicomponent reaction. [PDF]

Sci Adv
Hong S, Liu W, Zhang C, Yang X.
europepmc   +1 more source

Synthesis of 6- or 8-Carboxamido Derivatives of Imidazo[1,2-a]pyridines via a Heterogeneous Catalytic Aminocarbonylation Reaction. [PDF]

Molecules
Nagy E, Máriás A, Kovács M, Skoda-Földes R.   +3 more
europepmc   +1 more source

One-pot CuI/l-proline-catalysed multicomponent synthesis of pyrido[2',1':2,3]imidazo[4,5-<i>c</i>]quinoline derivatives from 2-(2-bromophenyl)imidazo[1,2-<i>a</i>]pyridines, NH₃ and DMSO under air. [PDF]

RSC Adv
Phuc BV, Thi Thuy D, Dao PA, Nguyen VL, Nguyen VH, Huy Nguyen H, Do DV, Nguyen H, Hung TQ, Dang TT.   +9 more
europepmc   +1 more source

Highly Enantioselective Lewis Acid Catalyzed Conjugate Addition of Imidazo[1,2-a]pyridines to α,β-Unsaturated 2-Acylimidazoles under Mild Conditions. [PDF]

J Org Chem
C Thedy ME, Pereira V, Dos Santos CR, Belli LPA, Franco MS, J Bortoluzzi A, Sandjo LP, Braga AL, F de Assis F.   +8 more
europepmc   +1 more source

One-pot synthesis of tetracyclic fused imidazo[1,2-a]pyridines via a three-component reaction. [PDF]

Beilstein J Org Chem, 2016
Yang B, Tao C, Shao T, Gong J, Che C.
europepmc   +1 more source

8-Aryl-6-chloro-3-nitro-2-(phenylsulfonylmethyl)imidazo[1,2-a]pyridines as potent antitrypanosomatid molecules bioactivated by type 1 nitroreductases. [PDF]

Eur J Med Chem, 2018
Fersing C, Boudot C, Pedron J, Hutter S, Primas N, Castera-Ducros C, Bourgeade-Delmas S, Sournia-Saquet A, Moreau A, Cohen A, Stigliani JL, Pratviel G, Crozet MD, Wyllie S, Fairlamb A, Valentin A, Rathelot P, Azas N, Courtioux B, Verhaeghe P, Vanelle P.   +20 more
europepmc   +1 more source

Ultrasound-assisted synthesis of imidazo[1,2-a]pyridines and sequential one-pot preparation of 3-selanyl-imidazo[1,2-a]pyridine derivatives

Arkivoc, 2019
Beatriz M. Vieira, Nathalia Padilha, Nelson M. Nascimento, Gelson Perin, Diego Alves, Ricardo F. Schumacher, Eder J. Lenardão   +6 more
openaire   +3 more sources