Technological innovations in photochemistry for organic synthesis: flow chemistry, high-throughput experimentation, scale-up, and photoelectrochemistry
L Buglioni, F Raymenants, A Slattery… - Chemical …, 2021 - ACS Publications
Photoinduced chemical transformations have received in recent years a tremendous amount
of attention, providing a plethora of opportunities to synthetic organic chemists. However …
of attention, providing a plethora of opportunities to synthetic organic chemists. However …
Photons or electrons? A critical comparison of electrochemistry and photoredox catalysis for organic synthesis
NES Tay, D Lehnherr, T Rovis - Chemical reviews, 2021 - ACS Publications
Redox processes are at the heart of synthetic methods that rely on either electrochemistry or
photoredox catalysis, but how do electrochemistry and photoredox catalysis compare? Both …
photoredox catalysis, but how do electrochemistry and photoredox catalysis compare? Both …
Comparative evaluation of light‐driven catalysis: A framework for standardized reporting of data
Light‐driven homogeneous and heterogeneous catalysis require a complex interplay
between light absorption, charge separation, charge transfer, and catalytic turnover. Optical …
between light absorption, charge separation, charge transfer, and catalytic turnover. Optical …
An organophotocatalytic late-stage N–CH 3 oxidation of trialkylamines to N-formamides with O 2 in continuous flow
MJP Mandigma, J Žurauskas, CI MacGregor… - Chemical …, 2022 - pubs.rsc.org
We report an organophotocatalytic, N–CH3-selective oxidation of trialkylamines in
continuous flow. Based on the 9, 10-dicyanoanthracene (DCA) core, a new catalyst (DCAS) …
continuous flow. Based on the 9, 10-dicyanoanthracene (DCA) core, a new catalyst (DCAS) …
Photoinduced Nickel-Catalyzed Selective N-Demethylation of Trialkylamines Using C(sp2)–Bromides as HAT Reagents
N-Demethylation of trialkylamines is a useful transformation, but typically requires harsh
reaction conditions and stepwise procedures, as well as judicious protection of labile …
reaction conditions and stepwise procedures, as well as judicious protection of labile …
Morphine alkaloids: History, biology, and synthesis
C Wicks, T Hudlicky, U Rinner - The Alkaloids: Chemistry and Biology, 2021 - Elsevier
This chapter provides a short overview of the history of morphine since it's isolation by
Sertürner in 1805. The biosynthesis of the title alkaloid as well as all total and formal …
Sertürner in 1805. The biosynthesis of the title alkaloid as well as all total and formal …
Endogenous opiates and behavior: 2022
RJ Bodnar - Peptides, 2023 - Elsevier
This paper is the forty-fifth consecutive installment of the annual anthological review of
research concerning the endogenous opioid system, summarizing articles published during …
research concerning the endogenous opioid system, summarizing articles published during …
N-Dealkylation of Amines
AA Najmi, R Bischoff, HP Permentier - Molecules, 2022 - mdpi.com
N-dealkylation, the removal of an N-alkyl group from an amine, is an important chemical
transformation which provides routes for the synthesis of a wide range of pharmaceuticals …
transformation which provides routes for the synthesis of a wide range of pharmaceuticals …
Sustainable photooxidation using a subpart-per-million heavy-metal-free red-light photocatalyst
M Lancel, T Golisano, C Monnereau… - ACS Sustainable …, 2023 - ACS Publications
Photochemical activation using red or near-infrared light has recently emerged as a
potential remedy for solving fundamental issues in photochemistry such as selectivity and …
potential remedy for solving fundamental issues in photochemistry such as selectivity and …
Electrochemical N-Demethylation of 14-Hydroxy Morphinans: Sustainable Access to Opioid Antagonists
The most challenging step in the preparation of many opioid antagonists is the selective N-
demethylation of a 14-hydroxymorphinan precursor. This process is carried out on a large …
demethylation of a 14-hydroxymorphinan precursor. This process is carried out on a large …