Z -isomerization of retinoids through combination of monochromatic photoisomerization and metal catalysis

Shirin Kahremany, Christopher Lane Sander, Gregory P. Tochtrop, Adam Kubas, Krzysztof Palczewski

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

Catalytic Z-isomerization of retinoids to their thermodynamically less stable Z-isomer remains a challenge. In this report, we present a photochemical approach for the catalytic Z-isomerization of retinoids using monochromatic wavelength UV irradiation treatment. We have developed a straightforward approach for the synthesis of Z-retinoids in high yield, overcoming common obstacles normally associated with their synthesis. Calculations based on density functional theory (DFT) have allowed us to correlate the experimentally observed Z-isomer distribution of retinoids with the energies of chemically important intermediates, which include ground- and excited-state potential energy surfaces. We also demonstrate the application of the current method by synthesizing gram-scale quantities of 9-cis-retinyl acetate 9Z-a. Operational simplicity and gram-scale ability make this chemistry a very practical solution to the problem of Z-isomer retinoid synthesis.

Original languageEnglish
Pages (from-to)8125-8139
Number of pages15
JournalOrganic and Biomolecular Chemistry
Volume17
Issue number35
DOIs
StatePublished - 21 Sep 2019
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2019 The Royal Society of Chemistry.

Funding

This work was supported in part by grants from the National Institutes of Health (NIH) (R24EY024864 and R24EY027283 to KP), RPB (Research to Prevent Blindness) to the Department of Ophthalmology at UCI, the Canadian Institute for Advanced Research (CIFAR), and the Alcon Research Institute (ARI). K. P. is the Leopold Chair of Ophthalmology. AK was supported by the Polish Ministry of Science and Higher Education from the budget allocations for science for years 2016–2019 within the IDEAS PLUS II project of number IdPII2015000164. Access to high performance computing resources was provided by the Interdisciplinary Centre for Mathematical and Computational Modelling in Warsaw, Poland, under grants no. G64-9 and GB77-11. The authors wish to acknowledge Allergan for their generous support of research at the Center for Translational Vision Research (CTVR) at Gavin Herbert Eye Institute, University of CA, Irvine.

FundersFunder number
Polish Ministry of Science and Higher EducationIdPII2015000164
National Institutes of HealthR24EY024864
National Eye InstituteR24EY027283
Research to Prevent Blindness
Canadian Institute for Advanced Research
Alcon Research Institute

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