Literature DB >> 32926512

Selective and Scalable Synthesis of Sugar Alcohols by Homogeneous Asymmetric Hydrogenation of Unprotected Ketoses.

Daniel J Tindall1, Steffen Mader2, Alois Kindler2, Frank Rominger3, A Stephen K Hashmi1,3, Thomas Schaub1,2.   

Abstract

Sugar alcohols are of great importance for the food industry and are promising building blocks for bio-based polymers. Industrially, they are produced by heterogeneous hydrogenation of sugars with H2 , usually with none to low stereoselectivities. Now, we present a homogeneous system based on commercially available components, which not only increases the overall yield, but also allows a wide range of unprotected ketoses to be diastereoselectively hydrogenated. Furthermore, the system is reliable on a multi-gram scale allowing sugar alcohols to be isolated in large quantities at high atom economy.
© 2020 Wiley-VCH GmbH.

Entities:  

Keywords:  asymmetric catalysis; hydrogenation; industrial chemistry; ruthenium; sugar alcohol

Year:  2020        PMID: 32926512     DOI: 10.1002/anie.202009790

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  1 in total

Review 1.  Recent Advances in C5 and C6 Sugar Alcohol Synthesis by Hydrogenation of Monosaccharides and Cellulose Hydrolytic Hydrogenation over Non-Noble Metal Catalysts.

Authors:  Elena Redina; Olga Tkachenko; Tapio Salmi
Journal:  Molecules       Date:  2022-02-17       Impact factor: 4.411

  1 in total

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