Sustainable chemo-enzymatic preparation of enantiopure (R)-β-hydroxy-1,2,3-triazoles via lactic acid bacteria-mediated bioreduction of aromatic ketones and a heterogeneous “click” cycloaddition reaction in deep eutectic solvents-Reference-Cited by-同舟云学术

Sustainable chemo-enzymatic preparation of enantiopure (R)-β-hydroxy-1,2,3-triazoles via lactic acid bacteria-mediated bioreduction of aromatic ketones and a heterogeneous “click” cycloaddition reaction in deep eutectic solvents

Published:2020 Issue:5 Volume:5 Page:859-864
ISSN:2058-9883
Container-title:Reaction Chemistry & Engineering
language:en
Short-container-title:React. Chem. Eng.

Author:

Vitale Paola¹²³⁴⁵^ORCID,Lavolpe Francesco¹²³⁴⁵,Valerio Francesca⁶⁴⁵^ORCID,Di Biase Mariaelena⁶⁴⁵^ORCID,Perna Filippo Maria¹²³⁴⁵^ORCID,Messina Eugenia⁷⁸⁹⁵¹⁰^ORCID,Agrimi Gennaro⁷⁸⁹⁵¹⁰^ORCID,Pisano Isabella⁷⁸⁹⁵¹⁰^ORCID,Capriati Vito¹²³⁴⁵^ORCID

Affiliation:

1. Dipartimento di Farmacia–Scienze del Farmaco

2. Università di Bari “A. Moro”

3. Consorzio C.I.N.M.P.I.S.

4. Bari

5. Italy

6. CNR Institute of Sciences of Food Production (ISPA)

7. Department of Biosciences, Biotechnologies and Biopharmaceutics

8. University of Bari

9. I-70125 Bari

10. CIRCC - Interuniversity Consortium Chemical Reactivity and Catalysis

Abstract

A chemo-enzymatic strategy for the preparation of enantiopure (R)-β-hydroxy-1,2,3-triazoles using a lactic acid bacterium as a whole-cell biocatalyst and a heterogeneous “click” cycloaddition reaction in deep eutectic solvents is disclosed.

Funder

Universita degli Studi di Bari Aldo Moro

Ministero dell’Istruzione, dell’Università e della Ricerca

Publisher

Royal Society of Chemistry (RSC)

Subject

Fluid Flow and Transfer Processes,Process Chemistry and Technology,Chemical Engineering (miscellaneous),Chemistry (miscellaneous),Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2020/RE/D0RE00067A

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2. Asymmetric Transfer Hydrogenation of α-Aminoalkyl α‘-Chloromethyl Ketones with Chiral Rh Complexes