Joydev Halder

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2012-2018 Indian Institute of Technology Kharagpur, Kharagpur, West Bengal, India 
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"Joydev Halder"
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Samik Nanda grad student 2012-2018 IIT Kharagpur
 (Synthetic exploration of ketoreductase from Klebsiella pneumoniae: Asymmetric synthesis of small ring carbocyclic, heterocyclic scaffolds and an indirect desymmetrization reaction.)
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Barik R, Halder J, Nanda S. (2019) Biocatalytic dynamic kinetic reductive resolution with ketoreductase from Klebsiella pneumoniae: the asymmetric synthesis of functionalized tetrahydropyrans. Organic & Biomolecular Chemistry
Halder J, Das D, Nanda S. (2018) A distinctive transformation based diversity oriented synthesis of small ring carbocycles and heterocycles from biocatalytically derived enantiopure α-substituted-β-hydroxyesters. Organic & Biomolecular Chemistry
Kumar R, Halder J, Nanda S. (2017) Asymmetric total synthesis of ( R )-α-cuparenone, ( S )-cuparene and formal synthesis of ( R )-β-cuparenone through Meinwald rearrangement and ring closing metathesis (RCM) reaction Tetrahedron. 73: 809-818
Kumar R, Rej RK, Halder J, et al. (2016) Enantiopure hydroxymethylated cycloalkenols as privileged small molecular multifunctional scaffolds for the asymmetric synthesis of carbocycles Tetrahedron Asymmetry. 27: 498-512
Halder J, Das D, Nanda S. (2015) Enantioselective biocatalytic reduction of 2,2-disubstituted ethylacetoacetates: An indirect desymmetrization approach for the synthesis of enantiopure (S)-4-hydroxy-3,3-disubstituted pentane-2-ones Tetrahedron Asymmetry. 26: 1197-1208
Das D, Halder J, Bhuniya R, et al. (2015) ChemInform Abstract: Stereoselective Synthesis of Enantiopure Oxetanes, a Carbohydrate Mimic, an ε-Lactone, and Cyclitols from Biocatalytically Derived β-Hydroxy Esters as Chiral Precursors. Cheminform. 46: no-no
Das D, Halder J, Bhuniya R, et al. (2014) Stereoselective Synthesis of Enantiopure Oxetanes, a Carbohydrate Mimic, an ϵ-Lactone, and Cyclitols from Biocatalytically Derived β-Hydroxy Esters as Chiral Precursors European Journal of Organic Chemistry. 2014: 5229-5246
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