Synthesis of spiroindolenines through a one-pot multistep process mediated by visible light

• Francesco Gambuti,
• Jacopo Pizzorno,
• Chiara Lambruschini,
• Renata Riva and
• Lisa Moni

Beilstein J. Org. Chem. 2024, 20, 2722–2731, doi:10.3762/bjoc.20.230

• Scheme 6. Based on the results reported by Zeitler [28], several mechanisms are involved in the oxidation of N-Ph-THIQ. The most probable involves the photoexcitation of the EDA (Electron Donor-Acceptor) complex promoting an electron transfer from N-Ph-THIQ to BrCCl3 to afford the amine radical cation

Generation of alkyl and acyl radicals by visible-light photoredox catalysis: direct activation of C–O bonds in organic transformations

• Mithu Roy,
• Bitan Sardar,
• Itu Mallick and
• Dipankar Srimani

Beilstein J. Org. Chem. 2024, 20, 1348–1375, doi:10.3762/bjoc.20.119

• radical cation. Then, the photogenerated thiocarbamate radical anion forms the alkyl radical by homolytic cleavage of the C–O bond. Next, the H-atom abstraction from iPr2NEt or the from the corresponding radical cation furnishes the desired product. In 2019, Aggarwal and co-workers [44] described a method

• catalyst is first excited and then transfers one electron to the thiocarbamate moiety to form a thiocarbamate radical anion, with change in oxidation state from III to IV. Next, the sacrificial electron donor Hünig base successfully converts [Ir(IV)] to [Ir(III)], with concurrent formation of an amine

Visible-light-mediated copper photocatalysis for organic syntheses

• Yajing Zhang,
• Qian Wang,
• Zongsheng Yan,
• Donglai Ma and
• Yuguang Zheng

Beilstein J. Org. Chem. 2021, 17, 2520–2542, doi:10.3762/bjoc.17.169

• ] discovered the photoinduced, copper-catalyzed cyanofluoroalkylation of alkenes and fluoroalkyl iodides 12. The reaction was initiated by the reduction of CuII with tertiary amines, which formed CuICN and an amine radical cation [55]. Under irradiation by ultraviolet light, CuICN was excited and transformed

Heterogeneous photocatalysis in flow chemical reactors

• Christopher G. Thomson,
• Ai-Lan Lee and
• Filipe Vilela

Beilstein J. Org. Chem. 2020, 16, 1495–1549, doi:10.3762/bjoc.16.125

Photocatalysis with organic dyes: facile access to reactive intermediates for synthesis

• Stephanie G. E. Amos,
• Marion Garreau,
• Luca Buzzetti and
• Jerome Waser

Beilstein J. Org. Chem. 2020, 16, 1163–1187, doi:10.3762/bjoc.16.103

• -opening driving force. N-Aryltetrahydroquinolines 34.1 have been intensively studied as a privileged scaffold for N-centred radical cation formations [138]. After iminium formation, formed by subsequent HAT on the amine radical cation, various nucleophiles can add, resulting in diverse functionalizations

Photocatalytic formation of carbon–sulfur bonds

• Alexander Wimmer and
• Burkhard König

Beilstein J. Org. Chem. 2018, 14, 54–83, doi:10.3762/bjoc.14.4

•  28) [63]. The reaction mechanism is different from the previous examples. The photoexcited state of Eosin Y can be quenched reductively by tertiary amines to form an Eosin Y radical anion and an amine radical cation. Molecular oxygen regenerates Eosin Y and is reduced to its superoxide radical anion

Eosin Y-catalyzed visible-light-mediated aerobic oxidative cyclization of N,N-dimethylanilines with maleimides

• Zhongwei Liang,
• Song Xu,
• Wenyan Tian and
• Ronghua Zhang

Beilstein J. Org. Chem. 2015, 11, 425–430, doi:10.3762/bjoc.11.48

• undergo an oxidative or reductive quenching cycle [48][49][50]. In this mechanism, a single electron transfer (SET) from 1 to 3EY* generates the amine radical cation 4, and at the same time, 3EY* is reduced to the EY•−. In the presence of oxygen, the photoredox catalytic cycle of EY is finished via a SET

Visible light mediated intermolecular [3 + 2] annulation of cyclopropylanilines with alkynes

• Theresa H. Nguyen,
• Soumitra Maity and
• Nan Zheng

Beilstein J. Org. Chem. 2014, 10, 975–980, doi:10.3762/bjoc.10.96

• % from 21. Mechanistically, the annulation with alkynes probably proceeds through a pathway similar to the one we proposed for the annulation with alkenes (Scheme 2) [29]. The photoexcited Ru(bpz)32+ oxidizes cyclopropylaniline 24 to the corresponding amine radical cation 25, which triggers the

• radical cation 29. Finally, Ru(bpz)31+ reduces amine radical cation 29 to the annulation product 30 while regenerating Ru(bpz)32+. The proposed mechanism accounts for lower reactivity of alkynes towards intermolecular addition of nucleophilic carbon-centered radicals as well as their regiochemistry in the

• cyclopropyl ring opening to generate distonic radical cation 26. The primary carbon radical of 26 adds to the terminal carbon of alkyne 27 to afford vinyl radical 28. Intramolecular addition of the vinyl radical to the iminium ion of distonic radical cation 28 closes the five membered ring and furnishes amine

The chemistry of amine radical cations produced by visible light photoredox catalysis

• Jie Hu,
• Jiang Wang,
• Theresa H. Nguyen and
• Nan Zheng

Beilstein J. Org. Chem. 2013, 9, 1977–2001, doi:10.3762/bjoc.9.234

• are emerging as a powerful tool in amine synthesis. This article reviews synthetic applications of amine radical cations produced by visible light photocatalysis. Keywords: α-amino radical; amine radical cation; catalysis; distonic ion; free radical; iminium ion; photoredox; visible light

• identification of the optimal solvent requires experimentation. Once formed, amine radical cation 2 has been shown to have four modes of reactivity. The first mode is the back electron transfer reaction, which involves amine radical cation 2 giving back one electron to M(n−1). This is a major side reaction

• /or irreversible downstream reactions of 2. The second mode involves hydrogen atom abstraction from 2 to produce iminium ion 4, when a good hydrogen atom acceptor is present in the reaction. The use of amine radical cation 2 as the source of a hydrogen radical has been applied to a number of visible

Spectroscopic characterization of photoaccumulated radical anions: a litmus test to evaluate the efficiency of photoinduced electron transfer (PET) processes

• Maurizio Fagnoni,
• Stefano Protti,
• Davide Ravelli and
• Angelo Albini

Beilstein J. Org. Chem. 2013, 9, 800–808, doi:10.3762/bjoc.9.91

• OXA due to conformational factors, in particular the steric bulk of the methyl groups. The more efficiently formed radicals scoop away traces of oxygen still present under these conditions. Likewise, in accordance with the role of amine radical cation deprotonation, is the fact that, of the two

Electron and hydrogen self-exchange of free radicals of sterically hindered tertiary aliphatic amines investigated by photo-CIDNP

• Martin Goez,
• Isabell Frisch and
• Ingo Sartorius

Beilstein J. Org. Chem. 2013, 9, 437–446, doi:10.3762/bjoc.9.46

• polarization thus constrains the amine-derived radical to have a lower g value than the sensitizer-derived radical. For the sensitizer XA this in only possible in the case of the neutral radical pairs because the g value of the amine radical cation (2.0037 [46]) is higher than the g values of the sensitizer

EPR and pulsed ENDOR study of intermediates from reactions of aromatic azides with group 13 metal trichlorides

• Giorgio Bencivenni,
• Riccardo Cesari,
• Daniele Nanni,
• Hassane El Mkami and
• John C. Walton

Beilstein J. Org. Chem. 2010, 6, 713–725, doi:10.3762/bjoc.6.84

• and forms the 4-aminodiaryl amine radical cation after loss of HX and (ii) formation of the aniline radical ArNH•, which couples with ArNH3+, ArNH2 or ArNH2+•. A plausible mechanism for formation of the dimer and trimer radical cations we observed is shown in Scheme 5 for the case of 2-methoxyaniline