Biplab Maji
M. Sc., Dr. rer. nat.
Dissertation
Reactivity parameters for understanding nucleophilic organocatalysis
(08/2012)[PDF]
Awards
Award of the Dr. Klaus Römer-Stiftung for PhD students (2012).
Publications
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, JustAccepted.
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Ambidente Reaktivität von Formaldehyd-N,N-dialkylhydrazonen
Ambident Reactivities of Formaldehyde N,N-Dialkylhydrazones

B. Maji, K. Troshin, H. Mayr, Angew. Chem. 2013, 125, 12116-12120; Angew. Chem. Int. Ed. 2013, 52, 11900-11904.

[deutsch-download][english-download]
Struktur und ambidente Reaktivität von Azolium-Enolaten
Structures and Ambident Reactivities of Azolium Enolates

B. Maji, H. Mayr, Angew. Chem. 2013, 125, 11370-11374; Angew. Chem. Int. Ed. 2013, 52, 11163-11167.

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Nucleophilic Reactivities of Schiff Bases
B. Maji, H. Mayr, Z. Naturforsch. B 2013, 68b, 693-699.

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Guanidines: Highly Nucleophilic Organocatalysts
B. Maji, M. Baidya, J. Ammer, S. Kobayashi, P. Mayer, A. R. Ofial, H. Mayr, Eur. J. Org. Chem. 2013, 3369-3377.

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A quantitative approach to nucleophilic organocatalysis
H. Mayr, S. Lakhdar, B. Maji, A. R. Ofial, Beilstein J. Org. Chem. 2012, 8, 1458-1478.
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Struktur und Reaktivität O-methylierter Breslow-Intermediate
Structures and Reactivities of O-Methylated Breslow Intermediates

B. Maji, H. Mayr, Angew. Chem. 2012, 124, 10554-10558; Angew. Chem. Int. Ed. 2012, 51, 10408-10412.
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Nucleophile Reaktivitäten von Desoxy-Breslow-Intermediaten: Wie beeinflusst Aromatizität die katalytische Aktivität N-heterocyclischer Carbene?
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. 2012, 124, 6335-6339; Angew. Chem. Int. Ed. 2012, 51, 6231-6235.
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Guanidines: Highly Nucleophilic Organocatalysts
B. Maji, D. S. Stephenson, H. Mayr, ChemCatChem 2012, 4, 993-999.

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Nukleophile Addition von Enolen und Enaminen an α,β-ungesättigte Acylazoliumionen: Mechanistische Studien
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. 2012, 124, 5325-5329; Angew. Chem. Int. Ed. 2012, 51, 5234-5238.
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Enamine aus Imidazolidinonen: Nucleophile mit geringer Reaktivität
Imidazolidinone-Derived Enamines: Nucleophiles with Low Reactivity

S. Lakhdar, B. Maji, H. Mayr, Angew. Chem. 2012, 124, 5837-5840; Angew. Chem. Int. Ed. 2012, 51, 5739-5742.
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Nucleophilicity Parameters of Enamides and their Implications for Organocatalytic Transformations
B. Maji, S. Lakhdar, H. Mayr, Chem. Eur. J. 2012, 18, 5732-5740.
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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.
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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.
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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.
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N-Heterocyclische Carbene: Organokatalysatoren mit mäßiger Nucleophilie, aber außerordentlich hoher Lewis-Basizität
N-Heterocyclic Carbenes: Organocatalysts with Moderate Nucleophilicity but Extraordinarily High Lewis Basisity
B. Maji, M. Breugst, H. Mayr, Angew. Chem. 2011, 123, 7047-7052; Angew. Chem. Int. Ed. 2011, 50, 6915-6919.
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