Data for Iron-Catalyzed Transfer Hydrogenation of Allylic Alcohols with Ethanol at Near Room Temperature
Original, unprocessed data for all novel compounds in the associated paper, "Iron-Catalyzed Transfer Hydrogenation of Allylic Alcohols with Ethanol at Near Room Temperature". This data provides supporting evidence for the formation of the proposed novel compounds synthesized using our methodology, including various alcohols. The alcohol-containing molecules formed serve as useful synthetic building blocks in organic synthesis. Data available includes 1H, 13C, and 19F Nuclear Magnetic Resonance (NMR) data, copies of mass spectrometry data, and copies of infra-red (IR) spectra.
Cite this dataset as:
Morrill, L.,
2026.
Data for Iron-Catalyzed Transfer Hydrogenation of Allylic Alcohols with Ethanol at Near Room Temperature.
Bath: University of Bath Research Data Archive.
Available from: https://doi.org/10.15125/BATH-01748.
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Data
Underpinning Data.zip
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Creative Commons: Attribution 4.0
Creators
Louis Morrill
University of Bath
Contributors
University of Bath
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Documentation
Data collection method:
Full experimental details for the preparation of each compound can be found in the Supplementary Information of the associated paper.
Technical details and requirements:
1H NMR, 13C NMR and 19F NMR spectra were obtained on a Bruker Avance, a Bruker Avance 400 (400 MHz 1H, 101 MHz 13C, 376 MHz 19F) or a Bruker Avance 500 (500 MHz 1H, 126 MHz 13C, 471 MHz 19F) spectrometer at room temperature in the solvent stated. Infrared spectra were recorded on a Shimadzu IRAffinity-1 Fourier Transform ATIR spectrometer as thin films using a Pike MIRacle ATR accessory. High-resolution mass spectrometric (HRMS) data were obtained on a Waters MALDI-TOF mx in Cardiff University.
Additional information:
NMR data are presented in the following format: chemical shift (multiplicity [s = singlet, br = broad, d = doublet, t = triplet, q = quartet, p = pentet dd = doublet of doublets, dt = doublet of triplets, dq = doublet of quartets, ddd = doublet of doublet of doublets, m = multiplet], coupling constant [in Hz], number of equivalent nuclei by integration). Spin-spin coupling constants J are given in Hz and refer to apparent multiplicities rather than true coupling constants. Data are reported as: chemical shift, multiplicity and integration. Infrared spectra were recorded with absorbance peaks quoted (νmax/cm-1).
Funders
University of Bath
https://doi.org/10.13039/501100000835
Cardiff University
https://doi.org/10.13039/501100000866
Publication details
Publication date: 10 November 2026
by: University of Bath
Version: 1
DOI: https://doi.org/10.15125/BATH-01748
URL for this record: https://researchdata.bath.ac.uk/1748
Related papers and books
Bari, M. A., AlQahtani, E. M., and Morrill, L. C., 2026. Iron-catalyzed transfer hydrogenation of allylic alcohols with ethanol at near room temperature. Organic & Biomolecular Chemistry. Available from: https://doi.org/10.1039/d6ob01654e.
Contact information
Please contact the Research Data Service in the first instance for all matters concerning this item.
Contact person: Louis Morrill
Faculty of Science
Chemistry