Joydev Halder - Publications

Affiliations: 
2012-2018 Indian Institute of Technology Kharagpur, Kharagpur, West Bengal, India 

8 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Maiti S, Parui N, Halder J, Dash J. Synthesis of triazole-fused tetracyclic spirooxindole derivatives metal-free Huisgen cycloaddition. Chemical Communications (Cambridge, England). PMID 39177038 DOI: 10.1039/d4cc02534b  0.35
2019 Barik R, Halder J, Nanda S. Biocatalytic dynamic kinetic reductive resolution with ketoreductase from Klebsiella pneumoniae: the asymmetric synthesis of functionalized tetrahydropyrans. Organic & Biomolecular Chemistry. PMID 31517368 DOI: 10.1039/C9Ob01681C  0.794
2018 Halder J, Das D, Nanda S. A distinctive transformation based diversity oriented synthesis of small ring carbocycles and heterocycles from biocatalytically derived enantiopure α-substituted-β-hydroxyesters. Organic & Biomolecular Chemistry. PMID 29569674 DOI: 10.1039/C8Ob00233A  0.801
2017 Kumar R, Halder J, Nanda S. 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. DOI: 10.1016/J.Tet.2016.12.072  0.759
2016 Kumar R, Rej RK, Halder J, Mandal H, Nanda S. Enantiopure hydroxymethylated cycloalkenols as privileged small molecular multifunctional scaffolds for the asymmetric synthesis of carbocycles Tetrahedron Asymmetry. 27: 498-512. DOI: 10.1016/J.Tetasy.2016.05.003  0.732
2015 Halder J, Das D, Nanda S. 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. DOI: 10.1016/J.Tetasy.2015.09.007  0.737
2015 Das D, Halder J, Bhuniya R, Nanda S. 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. DOI: 10.1002/CHIN.201509030  0.735
2014 Das D, Halder J, Bhuniya R, Nanda S. 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. DOI: 10.1002/Ejoc.201402521  0.69
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