We describe a templating/covalent capture strategy that enables photochemical formation of 8 cyclobutanes in one noncovalent assembly. This process was characterized by experiment and quantum mechanical/molecular mechanics (ONIOM) calculations. Thus, KI and 16 units of 5'-cinnamate guanosine form a G-quadruplex where C=C π bonds in neighboring G -quartets are separated by 3.3 Å, enabling [2+2] photocycloaddition in solution. This reaction is high-yielding (>90 %), regio- and diastereoselective. Since all components are in dynamic equilibrium this photocycloaddition is catalytic in K .
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http://dx.doi.org/10.1002/anie.201811202 | DOI Listing |
Chem Asian J
December 2024
IIT Bhilai: Indian Institute of Technology Bhilai, Chemistry, INDIA.
Investigating solid-state photoreactivity, driven by crystal packing, has been a major enduring research theme in Crystal Engineering. Trans-3-styryl pyridine (3-StPy), an unsymmetric olefin, is photo-stable. However, when converted to a series of salts, they exhibited solid-state photoreactivity under UV irradiation.
View Article and Find Full Text PDFChem Commun (Camb)
December 2024
School of Chemistry, University College Dublin, Science Centre South, Dublin 4, Ireland.
We report a continuous flow approach generating bicyclic cyclobutanes from unactivated alkenes in a metal-free manner that is inspired by the Kochi-Salomon reaction. A filtered Hg-lamp in combination with a simple flow set-up and acetone as UV light-absorbing co-solvent are crucial for this method thus showcasing attractive features for further exploitations.
View Article and Find Full Text PDFChem Sci
January 2025
Department of Chemistry, Indian Institute of Science Education and Research (IISER) Bhopal Academic Building - 2, Bhopal By-pass Road, Bhauri Bhopal-462066 India
Herein, we unveiled a regio- and diastereoselective synthesis of cyclobutylated phenothiazines, a unique class of structural congeners of phenothiazines visible-light-irradiated intermolecular [2 + 2]-cycloaddition reaction, from readily available naphthoquinones, 2-aminothiophenols, and styrenes, either in a two-step or three-component coupling process. By varying substitutions in all three coupling partners, a library of cyclobutylated phenothiazines, including late-stage derivatization with five commercial drugs, has been realized with up to 97% isolated yield. In contrast to the reported pathways, the developed [2 + 2]-photocycloaddition seems to proceed a 'photoinduced-electron-transfer' (PET) mechanism, which is well corroborated with the experimental observations, Rehm-Weller equation, and computation studies.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
U-M: University of Michigan, Department of Chemistry, 930 North University, 48109, Ann Arbor, UNITED STATES OF AMERICA.
Oxetanes are valuable motifs in medicinal chemistry applications, with demonstrated potential to serve as bioisosteres for an array of functional groups. Through the visible-light-mediated photoredox hydrodecarboxylation of 2-aryl oxetane 2-carboxylic acids this work enables access to the products of a [2+2]-photocycloaddition between alkenes and aryl aldehydes without the challenges associated with a traditional UV-light-mediated Paternò-Büchi reaction. Investigation into the hydrodecarboxylation mechanism reveals substrate-dependent modes of initiation under the conditions reported herein.
View Article and Find Full Text PDFOrg Lett
December 2024
Jiangsu Key Laboratory of Bioactive Natural Product Research and State Key Laboratory of Natural Medicines, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing 210009, People's Republic of China.
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