A modular, low footprint and scalable flow platform for the expedient α-aminohydroxylation of enolizable ketones-Reference-Cited by-同舟云学术

A modular, low footprint and scalable flow platform for the expedient α-aminohydroxylation of enolizable ketones

Published:2021 Issue:6 Volume:23 Page:2336-2351
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Kassin Victor-Emmanuel H.¹²³⁴⁵^ORCID,Morodo Romain¹²³⁴⁵,Toupy Thomas¹²³⁴⁵,Jacquemin Isaline¹²³⁴⁵,Van Hecke Kristof⁶⁷⁸⁹⁵^ORCID,Robiette Raphaël¹⁰¹¹¹²⁵^ORCID,Monbaliu Jean-Christophe M.¹²³⁴⁵^ORCID

Affiliation:

1. Center for Integrated Technology and Organic Synthesis

2. MolSys Research Unit

3. University of Liège

4. B-4000 Liège (Sart Tilman)

5. Belgium

6. XStruct

7. Department of Chemistry

8. Ghent University

9. B-9000 Ghent

10. Institute of Condensed Matter and Nanosciences

11. Université catholique de Louvain

12. 1348 Louvain-la-Neuve

Abstract

Taming reactive α-chloronitroso derivatives in flow for the preparation of advanced value-added chemicals through electrophilic amination.

Funder

Université de Liège

Fonds De La Recherche Scientifique - FNRS

Fonds pour la Formation à la Recherche dans l’Industrie et dans l’Agriculture

Fonds Wetenschappelijk Onderzoek

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/GC/D0GC04395H

Reference114 articles.

1. From glycals to aminosugars: a challenging test for new stereoselective aminohydroxylation and related methodologies

2. Modelling chemical kinetics of a complex reaction network of active pharmaceutical ingredient (API) synthesis with process optimization for benzazepine heterocyclic compound

3. Understanding and Kinetic Modeling of Complex Degradation Pathways in the Solid Dosage Form: The Case of Saxagliptin

4. Catalyst-free aza-Michael addition for C–N coupling in active pharmaceutical ingredient synthesis: Modelling of thermodynamic, reaction kinetics and mass transfer considerations

5. Continuous and convergent access to vicinyl amino alcohols

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