Evidence map›Paper›PMID 35652608›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2022

Recyclable Mn(I) Catalysts for Base-Free Asymmetric Hydrogenation: Mechanistic, DFT and Catalytic Studies.

Harikrishnan Jayaprakash, Peter Coburger, Michael Wörle, Antonio Togni, Hansjorg Grützmacher

Abstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Harikrishnan JayaprakashDepartment of Chemistry and Applied Biosiences, Swiss Federal Institute of Technology (ETH) Zürich, 8093, Zürich, Switzerland.ORCID http://orcid.org/0000-0003-4176-8510
Peter CoburgerDepartment of Chemistry and Applied Biosiences, Swiss Federal Institute of Technology (ETH) Zürich, 8093, Zürich, Switzerland.
Michael WörleDepartment of Chemistry and Applied Biosiences, Swiss Federal Institute of Technology (ETH) Zürich, 8093, Zürich, Switzerland.
Antonio TogniDepartment of Chemistry and Applied Biosiences, Swiss Federal Institute of Technology (ETH) Zürich, 8093, Zürich, Switzerland.
Hansjorg GrützmacherDepartment of Chemistry and Applied Biosiences, Swiss Federal Institute of Technology (ETH) Zürich, 8093, Zürich, Switzerland.

Funding

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung 200020-181966
6 · The paper itself

Abstract

We report here a mechanistic, DFT and catalytic study on a series of Mn(I) complexes 1, 2(a-d), 3, 4. The studies apprehended the requirements for Mn(I) complexes to be active in both asymmetric direct (AH) and transfer hydrogenations (ATH). The investigations disclosed 6 vital factors accelerating the formation of a resting species, which plays a significant role in lowering the activities of the Mn(I) complex 1 in ATH and AH, respectively. In addition, we also report here a base free Mn(I) catalyzed ATH of aryl alkyl ketones with high enantioselectivity (up to 98 % ee) and improved activity. More significantly, a novel and simple single-step process for recycling the resting species from the catalytic leftover has been discovered. Notably, the studies provide evidence for the existence of two different temperature dependent mechanisms for AH and ATH, in contrast to previous studies on related systems.

Indexed as

KetonesCatalysisHydrogenationKetonesasymmetric catalysisDFT studieshydrogenationmanganese-catalyzedmechanistic studies

Identifiers

PMID35652608
PMCPMC9540457

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.