PUBLICATIONS
71
A -conjugated covalent organic framework enables interlocked nickel/photoredox catalysis for light-harvesting cross-coupling reactions
Ayan Jati, Suranjana Dam,† Shekhar Kumar,† Kundan Kumar,† and Biplab Maji*
70
Asymmetric alkene-alkene reductive cross-coupling reaction via visible-light photoredox/cobalt dual catalysis
69
Direct C(3)5-H Polyfluoroarylation of 2-Amino/alkoxy Pyridines Enabled by a Transient Electron-deficient Palladium Intermediate
68
Sustainable Synthesis of α-Hydroxycarboxylic Acids by Manganese Catalyzed Acceptorless Dehydrogenative Coupling of Ethylene Glycol and Primary Alcohols
Angew. Chem.Int. Ed.2023,e202218329
Satyadeep Waiba^, Kakoli Maji^, Mamata Maity, Biplab Maji*
^Contributed Equally
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67
Book Chapter: "Transition Metal-Catalyzed C-H Functionalizations Using a Transient Directing Group Approach" in " Handbook of C-H Functionalization" Editor Debabrata Maiti (Wiley)
66
Ruthenium-Catalyzed Reductive Coupling of Epoxides with Primary Alcohols via Hydrogen Transfer Catalysis
J. Org. Chem. 2023, 88, 310−318
Akash Jana^, Sayandip Chakraborty^, Koushik Sarkar, Biplab Maji*
^Contributed Equally
65
Construction of 1,2,4-triazole-fused heterocycles via an amine oxidase-inspired catalyst
Org. Chem. Front., 2023,10, 480-489
Pradip Ramdas Thorve^, Kakoli Maji^, Biplab Maji*
^Contributed Equally
65
Construction of 1,2,4-triazole-fused heterocycles via an amine oxidase-inspired catalyst
Org. Chem. Front., 2023,10, 480-489
Pradip Ramdas Thorve^, Kakoli Maji^, Biplab Maji*
^Contributed Equally
64
Intermolecular dearomative [4+2] cycloaddition of naphthalenes via visible-light energy-transfer-catalysis
Chem. Sci., 2022,13, 12503-12510
Pramod Rai^, Kakoli Maji^, Sayan Kr Jana^, Biplab Maji*
^Contributed Equally
63
Dicarbofunctionalizations of an Unactivated Alkene via Photoredox/Nickel Dual Catalysis
62
Enantioselective C–H bond functionalization of aromatic ketones with 1,6-enynes via photoredox/cobalt dual catalysis
Chem. Commun., 2022,58, 9516-9519
Kakoli Maji^, Pradip Ramdas Thorve^, Pramod Rai, Biplab Maji*
^ Authors Contributed Equally
61
Manganese-Catalyzed Hydrogenation, Dehydrogenation, and Hydroelementation Reactions
Chem. Soc. Rev., 2022,51, 4386-4464
Kuhali Das^, Satyadeep Waiba^, Akash Jana, Biplab Maji
^ Authors Contributed Equally
60
Dual Metalation in a Two-Dimensional Covalent Organic Framework for Photocatalytic C–N Cross-Coupling Reactions
J. Am. Chem. Soc. 2022, 144, 7822-7833
Ayan Jati, Kaushik Dey, Maryam Nurhuda, Matthew A. Addicoat, Rahul Banerjee*, Biplab Maji*
59
Manganese-Catalyzed Reformation of Vicinal Glycols to α-Hydroxy Carboxylic Acids with the Liberation of Hydrogen Gas
58
Photoredox/Nickel Dual Catalysis Enables the Synthesis of Alkyl Cyclopropanes via C(sp3)–C(sp3) Cross Electrophile Coupling of Unactivated Alkyl Electrophiles
Org. Lett. 2022, 24, 1298-1302
Sayan K. Jana, Mamata Maity^, Purusattam Dey^, Biplab Maji*
^Authors Contributed Equally
57
Recent Development of Bis-Cyclometalated Chiral-at-Iridium and Rhodium Complexes for Asymmetric Catalysis
ACS Org. Inorg. Au 2022, 2, 99−125
Purusattam Dey^, Pramod Rai^, Biplab Maji*
^Authors Contributed Equally
56
Cooperative Lewis Acid Catalysis for the Enantioselective C(sp3 )−H Bond Functionalizations of 2‑Alkyl Azaarenes
Org. Lett. 2021, 23, 8888–8893
Pramod Rai, Satyadeep Waiba, Kakoli Maji, Dibyaranjan Sahoo, and Biplab Maji*
55
Advancements in multifunctional manganese complexes for catalytic hydrogen transfer reaction
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54
Manganese-Catalyzed Anti-Markovnikov Hydroamination of Allyl Alcohols via Hydrogen-Borrowing Catalysis
53
Nucleophilicities and Nucleofugalities of Thio- and Selenoethers
Biplab Maji, Xin-Hua Duan, Patrick M. Jüstel, Peter A. Byrne, Armin R. Ofial, Herbert Mayr*
52
Visible‐Light Mediated Metal‐Free Cross‐Electrophile Coupling of Isatin Derivatives with Electron‐Poor Alkenes
51
50
Phosphine-Free Manganese Catalyst Enables Selective Transfer Hydrogenation of Nitriles to Primary and Secondary Amines Using Ammonia−Borane
ACS. Catal. 2021, 11, 2786-2794
Koushik Sarkar^, Kuhali Das^, Abhisekh Kundu, Debashis Adhikari*, Biplab Maji*
^Authors Contributed Equally
49
Manganese catalyzed C-alkylation of methyl N-heteroarenes with primary alcohols
Chem. Commun. 2021, 57, 3026-3029
Akash Jana^, Amol Kumar^, Biplab Maji*
^Authors Contributed Equally
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48
The Emergence of Palladium‐Catalyzed C(sp3)‐H Functionalization of Free Carboxylic Acids
47
Deaminative Olefination of Methyl N‑Heteroarenes by an Amine Oxidase Inspired Catalyst
46
Aerobic primary and secondary amine oxidation cascade by a copper amine oxidase inspired catalyst
45
Manganese Catalysed α-Alkylation of Ketones with Secondary Alcohols Enables the Synthesis of β Branched Carbonyl Compounds
Chem. Commun. 2020, 56, 8376-8379
Satyadeep Waiba^, Sayan K. Jana^, Ayan Jati, Akash Jana, Biplab Maji*
^Authors contributed equally
44
Palladium-Catalyzed Remote C–H Functionalization of 2- Aminopyrimidines
43
A Phosphine-Free Manganese Catalyst Enables Stereoselective Synthesis of (1 + n) Membered Cycloalkanes from Methyl Ketones and 1,n-Diols
ACS Catal. 2020, 10, 2615-2626
Akash Jana, Kuhali Das, Abhishek Kundu, Pradip Ramdas Thorve, Debashis Adhikari*, and Biplab Maji*.
42
Basicities and Nucleophilicities of Pyrrolidines and Imidazolidinones Used as Organocatalysts
J. Am. Chem. Soc. 2020, 142, 1526-1547
Feng An, Biplab Maji, Elizabeth Min, Armin R. Ofial*, Herbert Mayr*
41
Manganese Catalyzed Acceptorless Dehydrogenative Coupling Reactions.
40
Synthesis and characterization of N,N-chelate manganese complexes and applications in C–N coupling reactions
39
Boron-Catalyzed N-Alkylation of Arylamines and Arylamides with Benzylic Alcohols
38
B(C6F5)3-Catalyzed Dehydrogenative Cyclization of N-Tosylhydrazones and Anilines via a Lewis Adduct: A Combined Experimental and Computational Investigations
Chem. Sci. 2019, 10, 7964-7974
Highlighted on SYNFORM- Thieme Chemistry
Murali Mohan Guru, Sriman De, Sayan Dutta, Debasis Koley*, Biplab Maji*
37
Manganese-Catalyzed Divergent Markovnikov Addition and [2+2+2] Cycloaddition of 2-Carbonyl Indanone with Terminal Alkyne
36
Photoredox/Cobalt Dual Catalysis for Visible-Light-Mediated Alkene–Alkyne Coupling
35
Base Metal-Catalyzed Direct Olefinations of Alcohols with Sulfones
34
Pyrene-affixed triazoles: a new class of molecular semiconductors for robust, non-volatile resistive memory devices
Chem. Commun. 2019, 55, 4643-4646
Biswajit K. Barman, Murali M. Guru. Gaurav K. Panda, Biplab Maji*, Ratheesh K. Vijayaraghavan*
33
Selective Hydroboration of Carboxylic Acids with a Homogeneous Manganese Catalyst
J. Org. Chem. 2019, 84, 1570-1579
Milan K. Barman^, Kuhali Das^, Biplab Maji*
^Authors contributed equally
32
Manganese-Catalyzed Acceptorless Dehydrogenative Coupling of Alcohols With Sulfones: A Tool To Access Highly Substituted Vinyl Sulfones
31
Manganese-Catalyzed Direct Olefination via an Acceptorless Dehydrogenative Coupling of Methyl Heteroarenes with Primary Alcohols
30
Manganese Catalyzed α-Alkylation of Nitriles with Primary Alcohols
Akash Jana^, C. Bal Reddy^, Biplab Maji*
^Authors contributed equally
29
Phosphine-Free NNN-Manganese Complex Catalyzed aAlkylation of Ketones with Primary Alcohols and Friedla¨nder Quinoline Synthesis
Adv. Synth. Catal. 2018, 360, 3233-3238
Milan K. Barman^, Akash Jana^, Biplab Maji*
^Authors contributed equally
28
Manganese Catalyzed Direct Olefination of Methylheteroarenes with Primary Alcohols
Angew. Chem. Int. Ed. 2018, 57, 9126-9130
Milan K. Barman, Satyadeep Waiba, Biplab Maji*
Highlighted on Synfacts
27
Recent Developments of Manganese Complexes for Catalytic Hydrogenation and Dehydrogenation Reactions
S. Mukherjee^, B. Maji^, A Tlahuext-Aca, F Glorius*, J. Am. Chem. Soc. 2016, 138, 16200 – 16203.
^ This two author contributed equally.
25. Ruthenium-NHC Catalyzed α-Alkylation of Methylene Ketones Provides Branched Products through Borrowing Hydrogen Strategy
C. Schlepphorst, B. Maji, F. Glorius*, ACS Catalysis 2016, 6, 4184 – 4188.
24. Catalytic Enantioselective Nitroso Diels-Alder Reaction
B. Maji*, H. Yamamoto*, J. Am. Chem. Soc. 2015, 137, 15957–15963.
23. Use of In Situ Generated Nitrosocarbonyl Compounds in Catalytic Asymmetric a-Amination and a-Hydroxylation Reactions
B. Maji*, H. Yamamoto*, Bull. Chem. Soc. Jpn. 2015, 88, 753–762.
Selected as Cover Page.
22.Asymmetric Synthesis of Tertiary a-Hydroxy Phosphonic Acid Derivatives under Aerobic Oxidation Condition
B. Maji*, H. Yamamoto*, Synlett. 2015, 26, 1528–1532.
21.Scales of Lewis Basicities toward C-centered Lewis Acids (Carbocations)
H. Mayr*, J. Ammer, M. Baidya, B. Maji, T. A. Nigst, A. R. Ofial, T. Singer, J. Am. Chem. Soc. 2015, 137, 2580–2599.
Selected as Cover Page.
Highlighted as Spotlights.
20. Copper-Catalyzed Asymmetric Synthesis of Tertiary a-Hydroxy Phosphonic Acid Derivatives with In Situ Generated Nitrosocarbonyl Compounds as the Oxygen Source
B. Maji*, H. Yamamoto*, Angew. Chem. Int. Ed. 2014, 53, 14472–14475.
Selected as Hot Paper by Angewandte Chemie.
19. Asymmetric construction of quaternary stereocenters by magnesium catalysed direct amination of b-ketoesters using in situ generated nitrosocarbonyl compounds as nitrogen sources
B. Maji*, M. Baidya, H. Yamamoto*, Chem. Sci. 2014, 5, 3941–3945.
Highlighted in SynFacts.
18. Proline-Tetrazole-Catalyzed Enantioselective N-Nitroso Aldol Reaction of Aldehydes with In Situ Generated Nitrosocarbonyl Compounds
B. Maji*, H. Yamamoto*, Angew. Chem. Int. Ed. 2014, 53, 8714–8717.
Highlighted in SynFacts.
17. Ambident Reactivities of Formaldehyde N,N-Dialkylhydrazones
B. Maji*, K. Troshin, H. Mayr*, Angew. Chem. Int. Ed. 2013, 52, 11900–11904.
16. Structures and Ambident Reactivities of Azolium Enolates
B. Maji*, H. Mayr*, Angew. Chem. Int. Ed. 2013, 52, 11163–11167
15. Nucleophilic Reactivities of Schiff Bases
B. Maji, H. Mayr*, Z. Naturforsch B. 2013, 68b, 693–699.
14.Nucleophilic reactivities of 2-imidazolines and related N-heterocyclic compounds
B. Maji, M. Baidya, J. Ammer, S. Kobayashi, P. Mayer, A. R. Ofial, H. Mayr*, Eur. J. Org. Chem. 2013, 2013, 3369–3377.
13. A quantitative approach to nucleophilic organocatalysis
H. Mayr*, S. Lakhdar, B. Maji, A. R. Ofial, Beilstein J. Org. Chem. 2012, 8, 1458–1478.
12. Structures and Reactivities of O-Methylated Breslow Intermediates
B. Maji, H. Mayr*, Angew. Chem. Int. Ed. 2012, 51, 10408–10412.
11. (E)-5-(Methoxy(phenyl)methylene)-1,3,4-triphenyl-4,5-dihydro- 1H-1,2,4-triazole
B. Maji, G. Berionni, H. Mayr, P. Mayer*, Acta Crystallogr., Sect. E: Struct. Rep. Online 2012, 68, o3307.
10. (Z)-2-[Methoxy(phenyl)methylidene]-3,4,5-trimethyl-2,3-dihydro-1,3-thiazole
B. Maji, H. Mayr, P. Mayer*, Acta Crystallogr., Sect. E: Struct. Rep. Online 2012, 68, o2644.
9. Nucleophilic Reactivity of Deoxy-Breslow-Intermediates: How Does Aromaticity Affect the Catalytic Activity of N-Heterocyclic Carbenes?
B. Maji, M. Horn, H. Mayr*, Angew. Chem. Int. Ed. 2012, 51, 6231–6235.
Selected as Hot Paper by Angewandte Chemie.
8. Guanidines: Highly Nucleophilic Organocatalysts
B. Maji, D. S. Stephenson, H. Mayr*, ChemCatChem 2012, 4, 993–999.
7. Imidazolidinone-Derived Enamines: Nucleophiles with Low Reactivity
S. Lakhdar*, B. Maji, H. Mayr*, Angew. Chem. Int. Ed. 2012, 51, 5739–5742.
Selected as Hot Paper by Angewandte Chemie.
6. Nucleophilic Addition of Enols and Enamines to α,β-Unsaturated Acyl Azoliums: Mechanistic Studies
R. C. Samanta, B. Maji, S. De Sarkar, K. Bergander, R. Fröhlich, C. Mück-Lichtenfeld*, H. Mayr*, A. Studer*, Angew. Chem. Int. Ed. 2012, 51, 5234–5238.
5. Nucleophilicity Parameters of Enamides and their Implications for Organocatalytic Transformations
B. Maji, S. Lakhdar, H. Mayr*, Chem. Eur. J. 2012, 18, 5732-5740.
4. Nucleophilicity parameters for designing transition metal-free C-C bond forming reactions of organoboron compounds
G. Berionni, B. Maji, P. Knochel*, H. Mayr*, Chem. Sci. 2012, 3, 878-882.
3. Characterization of the nucleophilic reactivities of thiocarboxylate, dithiocarbonate and dithiocarbamate anions
X.-H. Duan, B. Maji, H. Mayr*, Org. Biomol. Chem. 2011, 9, 8046-8050.
2. Nucleophilicities and Lewis Basicities of Isothiourea Derivatives
B. Maji, C. Joannesse, T. A. Nigst, A. D. Smith, H. Mayr*, J. Org. Chem. 2011, 76, 5104–5112.
1. N-Heterocyclic Carbenes: Organocatalysts with Moderate Nucleophilicity but Extraordinarily High Lewis Basicity
B. Maji, M. Breugst, H. Mayr*, Angew. Chem. Int. Ed. 2011, 50, 6915–6919.
Selected as Hot Paper by Angewandte Chemie.