Evidence map›Paper›PMID 35700045›Full record

ArticleAngewandte Chemie (International ed. in English)2022

Enantioselective Synthesis of Enantioisotopomers with Quantitative Chiral Analysis by Chiral Tag Rotational Spectroscopy.

Mitchell D Mills, Reilly E Sonstrom, Zoua Pa Vang, Justin L Neill, Haley N Scolati, Channing T West, Brooks H Pate, Joseph R Clark

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
  2. Interstellar Stereoisomerism.ACS earth & space chemistry · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Highly selective catalytic transfer hydrodeuteration of cyclic alkenes.Journal of labelled compounds & radiopharmaceuticals · 2023
    Article
  17. 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

8 authors.

Mitchell D MillsDepartment of Chemistry, Marquette University, Milwaukee, WI 53233, USA.
Reilly E SonstromDepartment of Chemistry, University of Virginia, Charlottesville, VA 22904, USA.ORCID 0000-0003-0497-6660
Zoua Pa VangDepartment of Chemistry, Marquette University, Milwaukee, WI 53233, USA.
Justin L NeillBrightSpec Inc., 770 Harris Street Suite 104b, Charlottesville, VA 22903, USA.ORCID 0000-0003-0964-3275
Haley N ScolatiDepartment of Chemistry, University of Virginia, Charlottesville, VA 22904, USA.
Channing T WestDepartment of Chemistry, University of Virginia, Charlottesville, VA 22904, USA.
Brooks H PateDepartment of Chemistry, University of Virginia, Charlottesville, VA 22904, USA.ORCID 0000-0002-6097-7230
Joseph R ClarkDepartment of Chemistry, Marquette University, Milwaukee, WI 53233, USA.ORCID 0000-0002-3081-5732

Funding

High Field Electrospray/MALDI Fourier Transform Mass SpectrometerS10RR029517 · NCRR · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI WOOD, TROY D · 2010 to 2010
$1.7M
NCRR NIH HHS S10 RR029517
6 · The paper itself

Abstract

Fundamental to the synthesis of enantioenriched chiral molecules is the ability to assign absolute configuration at each stereogenic center, and to determine the enantiomeric excess for each compound. While determination of enantiomeric excess and absolute configuration is often considered routine in many facets of asymmetric synthesis, the same determinations for enantioisotopomers remains a formidable challenge. Here, we report the first highly enantioselective metal-catalyzed synthesis of enantioisotopomers that are chiral by virtue of deuterium substitution along with the first general spectroscopic technique for assignment of the absolute configuration and quantitative determination of the enantiomeric excess of isotopically chiral molecules. Chiral tag rotational spectroscopy uses noncovalent chiral derivatization, which eliminates the possibility of racemization during derivatization, to perform the chiral analysis without the need of reference samples of the enantioisotopomer.

Indexed as

StereoisomerismSpectrum AnalysisChiralityCopperEnantioisotopomersRotational SpectroscopyTransfer Hydrodeuteration

Identifiers

PMID35700045
PMCPMC9403034

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.