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Keshab Mondal - Publications

Affiliations: 
2012-2018 IIT Guwahati 
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7 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
2018 Mondal K, Pan SC. Organocatalytic Asymmetric Domino Michael/Acyl Transfer Reaction between γ/δ-Hydroxyenones and α-Nitroketones. The Journal of Organic Chemistry. PMID 29634262 DOI: 10.1021/Acs.Joc.8B00436  0.676
2017 Mondal K, Pan SC. Synthesis of 2,5-Disubstituted Furans from Sc(OTf)3 Catalyzed Reaction of Aryl Oxiranediesters with γ-Hydroxyenones. The Journal of Organic Chemistry. PMID 28332838 DOI: 10.1021/Acs.Joc.7B00133  0.674
2017 Mondal B, Mondal K, Satpati P, Pan SC. Organocatalytic Asymmetric Dimerization of γ-Hydroxyenones to Acetals and Theoretical Investigations into the Diastereoselection European Journal of Organic Chemistry. 2017: 7101-7106. DOI: 10.1002/Ejoc.201701439  0.606
2017 Mondal K, Pan SC. Lewis Acid Catalyzed [3+3] Annulation of Donor-Acceptor Cyclopropanes with γ-Hydroxyenones: Access to Highly Functionalized Tetrahydropyrans European Journal of Organic Chemistry. 2017: 534-537. DOI: 10.1002/Ejoc.201601305  0.679
2016 Mondal K, Mondal B, Pan SC. Organocatalytic redox isomerization of electron-deficient allylic alcohols: Synthesis of 1,4-ketoaldehydes. The Journal of Organic Chemistry. PMID 27163844 DOI: 10.1021/Acs.Joc.6B00243  0.621
2015 Mondal K, Pan SC. Copper(I)-Catalyzed (Z)-β-(Tosyloxy)alkenyl Iodide Synthesis from (Aryl)[(E)-β-(tosyloxy)alkenyl]iodonium Tosylates: Diversity-Oriented Synthesis of Trisubstituted Alkenes European Journal of Organic Chemistry. 2015: 2129-2132. DOI: 10.1002/Ejoc.201500039  0.641
2015 Mondal K, Pan SC. ChemInform Abstract: Copper(I)-Catalyzed (Z)-β-(Tosyloxy)alkenyl Iodide Synthesis from (Aryl)[(E)-β-(tosyloxy)alkenyl]iodonium Tosylates: Diversity-Oriented Synthesis of Trisubstituted Alkenes. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201530039  0.586
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