Literature DB >> 33891819

Reducing Challenges in Organic Synthesis with Stereoselective Hydrogenation and Tandem Catalysis.

Patrick D Parker1, Xintong Hou1, Vy M Dong1.   

Abstract

Tandem catalysis enables the rapid construction of complex architectures from simple building blocks. This Perspective shares our interest in combining stereoselective hydrogenation with transformations such as isomerization, oxidation, and epimerization to solve diverse challenges. We highlight the use of tandem hydrogenation for preparing complex natural products from simple prochiral building blocks and present tandem catalysis involving transfer hydrogenation and dynamic kinetic resolution. Finally, we underline recent breakthroughs and opportunities for asymmetric hydrogenation.

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Year:  2021        PMID: 33891819      PMCID: PMC9141585          DOI: 10.1021/jacs.1c00750

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   16.383


  220 in total

Review 1.  The cyclization of peptides and depsipeptides.

Authors:  John S Davies
Journal:  J Pept Sci       Date:  2003-08       Impact factor: 1.905

Review 2.  Asymmetric hydrogenation of minimally functionalised terminal olefins: an alternative sustainable and direct strategy for preparing enantioenriched hydrocarbons.

Authors:  Oscar Pàmies; Pher G Andersson; Montserrat Diéguez
Journal:  Chemistry       Date:  2010-12-27       Impact factor: 5.236

Review 3.  Iridium-catalyzed asymmetric hydrogenation of olefins.

Authors:  Stephen J Roseblade; Andreas Pfaltz
Journal:  Acc Chem Res       Date:  2007-08-03       Impact factor: 22.384

4.  Dynamic kinetic resolution allows a highly enantioselective synthesis of cis-alpha-aminocycloalkanols by ruthenium-catalyzed asymmetric hydrogenation.

Authors:  Sheng Liu; Jian-Hua Xie; Li-Xin Wang; Qi-Lin Zhou
Journal:  Angew Chem Int Ed Engl       Date:  2007       Impact factor: 15.336

5.  Looking forward in pharmaceutical process chemistry.

Authors:  Ian W Davies; Christopher J Welch
Journal:  Science       Date:  2009-08-07       Impact factor: 47.728

6.  Highly Selective Hydrogenation of Aromatic Ketones and Phenols Enabled by Cyclic (Amino)(alkyl)carbene Rhodium Complexes.

Authors:  Yu Wei; Bin Rao; Xuefeng Cong; Xiaoming Zeng
Journal:  J Am Chem Soc       Date:  2015-07-16       Impact factor: 15.419

7.  Tandem rhodium catalysis: exploiting sulfoxides for asymmetric transition-metal catalysis.

Authors:  K G M Kou; V M Dong
Journal:  Org Biomol Chem       Date:  2015-06-07       Impact factor: 3.876

8.  Branching Out: Rhodium-Catalyzed Allylation with Alkynes and Allenes.

Authors:  Philipp Koschker; Bernhard Breit
Journal:  Acc Chem Res       Date:  2016-07-25       Impact factor: 22.384

9.  Stereoselectivity in Asymmetric Catalysis: The Case of Ruthenium-Catalyzed Ketone Hydrogenation.

Authors:  Elaine Limé; Michelle D Lundholm; Aaron Forbes; Olaf Wiest; Paul Helquist; Per-Ola Norrby
Journal:  J Chem Theory Comput       Date:  2014-06-10       Impact factor: 6.006

10.  Accessing (Multi)Fluorinated Piperidines Using Heterogeneous Hydrogenation.

Authors:  Tobias Wagener; Arne Heusler; Zackaria Nairoukh; Klaus Bergander; Constantin G Daniliuc; Frank Glorius
Journal:  ACS Catal       Date:  2020-09-18       Impact factor: 13.084

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  3 in total

1.  Asymmetric hydrogenation for the synthesis of 2-substituted chiral morpholines.

Authors:  Mingxu Li; Jian Zhang; Yashi Zou; Fengfan Zhou; Zhenfeng Zhang; Wanbin Zhang
Journal:  Chem Sci       Date:  2021-10-28       Impact factor: 9.825

2.  Access to Unexplored 3D Chemical Space: cis-Selective Arene Hydrogenation for the Synthesis of Saturated Cyclic Boronic Acids.

Authors:  Akash Kaithal; Tobias Wagener; Peter Bellotti; Constantin G Daniliuc; Lisa Schlichter; Frank Glorius
Journal:  Angew Chem Int Ed Engl       Date:  2022-07-04       Impact factor: 16.823

3.  Highly Selective Hydrogenation of C═C Bonds Catalyzed by a Rhodium Hydride.

Authors:  Yiting Gu; Jack R Norton; Farbod Salahi; Vladislav G Lisnyak; Zhiyao Zhou; Scott A Snyder
Journal:  J Am Chem Soc       Date:  2021-06-18       Impact factor: 16.383

  3 in total

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