Browsing by Author Babu, S.A.

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Issue DateTitleGuideTypeAuthor(s)
2012Magnetic nano Fe3O4 and CuFe2O4 as heterogeneous catalysts: A green method for the stereo- and regioselective reactions of epoxides with indoles/pyrroles-ArticleParella, R.; Naveen; Babu, S.A.
2014Magnetic Nano Fe3O4 Catalyzed Solvent-Free Stereo- and Regioselective ­Aminolysis of Epoxides by Amines; a Green Method for the Synthesis of β-Amino Alcohols-ArticleKumar, Amit; Parella, R.; Babu, S.A.
2014Magnetically Separable Nano Fe3O4 Catalyzed Direct Azidation of Allylic and Benzylic Alcohols Followed by Copper-Catalyzed Click Reaction-ArticleAslam, N.A.; Babu, S.A.; Singh, Dharmendra Kumar; Rana, A.
2016Multicomponent reaction comprising one-pot installation of bidentate directing group and Pd(II)-catalyzed direct β-arylation of C(sp3)single bondH bond of aliphatic and alicyclic carboxamides-ArticleMohan, Sruthi; Gopalakrishnan, B.; Babu, S.A.
2019One-pot, solvent-free Pd(II)-catalyzed direct β-C-H arylation of carboxamides involving anhydrides as substrates via in situ installation of directing group-ArticleDalal, A.; Singh, Prabhakar; Babu, S.A.
2019Palladium(II)‐Catalyzed Sp3/Sp2γ‐ and δ‐C‐H Functionalization of Aryl Amines using 5‐Methylisoxazole‐3‐Carboxamide as Directing Group-ArticleSingh, Prabhakar; Dalal, A.; Babu, S.A.
2016Palladium(II)‐Promoted Directing Group‐Enabled Regioselective C‐H Arylation of The C‐3 Position of 2‐ or 3‐(Aminoalkyl)‐Thiophene and Furfurylamine Derivatives-ArticleRajkumar, V.; Naveen; Babu, S.A.
2014Palladium-Catalyzed Double Activation and Arylation of 2° and 3° C(sp3)–H Bonds of the Norbornane System: Formation of a C–C Bond at the Bridgehead Carbon and Bridgehead Quaternary Stereocenter-ArticleParella, R.; Babu, S.A.
2019Palladium‐Catalyzed 8‐Aminoquinoline‐Aided sp2δ‐C−H Intramolecular Amidation/Annulation: A Route to Tricyclic Quinolones-ArticlePadmavathi, R.; Babu, S.A.
2017Pd(II)-Catalyzed Arylation and Intramolecular Amidation of γ-C(sp3)-H Bonds: En Route to Arylheteroarylmethane and Pyrrolidone Ring Annulated Furan/Thiophene Scaffolds-ArticleParella, R.; Babu, S.A.
2016Pd(II)-Catalyzed Bidentate Directing Group-Aided Chemoselective Acetoxylation of Remote ε-C(sp2)–H Bonds in Heteroaryl–Aryl-Based Biaryl Systems-ArticleNaveen; Rajkumar, V.; Babu, S.A.; Gopalakrishnan, B.
2017Pd(II)-Catalyzed, Picolinamide-Assisted, Z-Selective γ-Arylation of Allylamines to Construct Z-Cinnamylamines-ArticleParella, R.; Babu, S.A.
2020Pd(II)‐Catalyzed, Bidentate Directing Group‐aided Alkylation of sp3 γ‐C−H Bonds: Access to 3‐Alkylated Thiophene/Furan and Benzothiophene/Benzofuran Motifs-ArticleBisht, Narendra; Babu, S.A.; Tomar, R.
2015Pd(OAc)2-Catalyzed, AgOAc-Promoted Z Selective Directed β-Arylation of Acrylamide Systems and Stereoselective Construction of Z-Cinnamamide Scaffolds-ArticleParella, R.; Babu, S.A.
2015Pd(OAc)2/AgOAc catalytic system based bidentate ligand directed regiocontrolled C-H arylation and alkylation of the C-3 position of thiophene- and furan-2-carboxamides-ArticlePadmavathi, R.; Sankar, Rathinam; Gopalakrishnan, B.; Parella, R.; Babu, S.A.
2019Pd‐Catalyzed Diastereoselective Intramolecular Amide α‐C−H Arylation in Sterically Hindered Monospirooxindole Motifs-ArticleShukla, D.; Babu, S.A.
2013RCM strategy-based entry into new crown ether/polyether macrocyclic systems derived from hydroxy benzaldehydes-ArticleNaveen; Parella, R.; Babu, S.A.
2016Regio- and diastereoselective construction of a new set of functionalized pyrrolidine, spiropyrrolidine and spiropyrrolizidine scaffolds appended with aryl- and heteroaryl moieties via the azomethine ylide cycloadditions-ArticleRajkumar, V.; Babu, S.A.; Padmavathi, R.
2014Regio- and Diastereoselective Cycloaddition of Azomethine Ylides with Benzylidenemalononitrile: Assembly of a New Set of Multisubstituted 4,4-Dicyanopyrrolidine-2-carboxylate and Nornicotine Scaffolds-ArticleRajkumar, V.; Babu, S.A.
2015Regio- and stereoselective Pd-catalyzed direct arylation of unactivated sp3 C(3)-H bonds of tetrahydrofuran and 1,4-benzodioxane systems-ArticleParella, R.; Babu, S.A.