Biplab Maji

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
	Nucleophilicities and Nucleofugalities of Thio- and Selenoethers B. Maji, X.-H. Duan, P. M. Jüstel, P. A. Byrne, A. R. Ofial, H. Mayr, Chem. Eur. J. 2021, Accepted Article (doi: 10.1002/chem.202100977). [download]
	Basicities and Nucleophilicities of Pyrrolidines and Imidazolidinones Used as Organocatalysts F. An, B. Maji, E. Min, A. R. Ofial, H. Mayr, J. Am. Chem. Soc. 2020, 142, 1526-1547. [download]
	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. [download]
	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. [deutsch-download][english-download]
	Nucleophilic Reactivities of Schiff Bases B. Maji, H. Mayr, Z. Naturforsch. B 2013, 68b, 693-699. [download]
	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. [download]
	A quantitative approach to nucleophilic organocatalysis H. Mayr, S. Lakhdar, B. Maji, A. R. Ofial, Beilstein J. Org. Chem. 2012, 8, 1458-1478. [download]
	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. [deutsch-download][english-download]
	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. [deutsch-download][english-download]
	Guanidines: Highly Nucleophilic Organocatalysts B. Maji, D. S. Stephenson, H. Mayr, ChemCatChem 2012, 4, 993-999. [download]
	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. [deutsch-download][english-download]
	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. [deutsch-download][english-download]
	Nucleophilicity Parameters of Enamides and their Implications for Organocatalytic Transformations B. Maji, S. Lakhdar, H. Mayr, Chem. Eur. J. 2012, 18, 5732-5740. [download]
	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. [download]
	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. [download]
	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. [download]
	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. [deutsch-download] [english-download]