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A One-Pot Chemoenzymatic Strategy Combining Promiscuous Lipase Catalysis and Zn-Mediated Reduction to Access Tryptamine Derivatives
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inferredcites →https://doi.org/10.1002/(sici)1097-461x(1998)69:1<89::aid-qua11>3.0.co;2-0openalex-snapshot
Ab initio and density functional theory studies of the catalytic mechanism for ester hydrolysis in serine hydrolases
inferredcites →https://doi.org/10.1002/ajoc.202300427openalex-snapshot
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inferredcites →https://doi.org/10.1002/anie.202006648openalex-snapshot
Biocatalysis: Enzymatic Synthesis for Industrial Applications
inferredcites →https://doi.org/10.1002/cctc.201601583openalex-snapshot
Friedel–Crafts Alkylation of Indoles with Nitroalkenes through Hydrogen‐Bond‐Donating Metal–Organic Framework
inferredcites →https://doi.org/10.1002/cctc.202401182openalex-snapshot
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inferredcites →https://doi.org/10.1007/s10967-013-2816-0openalex-snapshot
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inferredcites →https://doi.org/10.1007/s11696-023-02979-xopenalex-snapshot
Copper-catalyzed alkylation reactions of indole: An overview
inferredcites →https://doi.org/10.1007/s13399-020-00695-0openalex-snapshot
Promotion of water in BPL-catalyzed asymmetric cross aldol reaction
inferredcites →https://doi.org/10.1016/j.apcata.2008.01.030openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.bej.2015.04.021openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.bmc.2010.06.058openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.bmc.2012.08.021openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.bmc.2012.09.027openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejps.2016.05.025openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.tet.2020.131643openalex-snapshot
First biocatalytic Groebke-Blackburn-Bienaymé reaction to synthesize imidazo[1,2-a]pyridine derivatives using lipase enzyme
inferredcites →https://doi.org/10.1016/j.tetlet.2013.11.047openalex-snapshot
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inferredcites →https://doi.org/10.1039/c8ra01397gopenalex-snapshot
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inferredcites →https://doi.org/10.1039/d1cs00065aopenalex-snapshot
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inferredcites →https://doi.org/10.1039/d1nj06232hopenalex-snapshot
First biocatalytic synthesis of piperidine derivatives via an immobilized lipase-catalyzed multicomponent reaction
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inferredcites →https://doi.org/10.1080/00397911.2018.1554745openalex-snapshot
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inferredcites →https://doi.org/10.2174/138527209789578126openalex-snapshot
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inferredcites →https://doi.org/10.2174/1568026616666160927150839openalex-snapshot
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inferredcites →https://doi.org/10.2174/1570163820666230505120553openalex-snapshot
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Stereoselective Promiscuous Reactions Catalyzed by Lipases
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