210 research outputs found
ELECTROCHEMICAL DATA FOR EVALUATION OF PRACTICALLY IMPORTANT PROPERTIES OF ORGANIC AND ORGANOMETALLIC COMPOUNDS
The research was supported by the Ministry of Science and Higher Education of the Russian Federation at FRC Kazan Scientific Center (grant No. 075-15-2022-1128)
Excited State Energy Distribution and Redistribution and Chemical Reactivity; Mechanistic and Exploratory Organic Photochemistry <i>J. Am. Chem. </i><i>Soc.</i> <b>2000</b>, <i>122</i>, 952−953.
Excited State Energy Distribution and Redistribution and Chemical Reactivity; Mechanistic and Exploratory Organic Photochemistry<sup>1,2</sup>
Excited State Energy Distribution and Redistribution and Chemical Reactivity; Mechanistic and Exploratory Organic Photochemistry<sup>1,2</sup>
Excited State Energy Distribution and Redistribution
and Chemical Reactivity; Mechanistic and
Exploratory Organic Photochemistry1,2</sup
Photocyclization of Alkenes and Arenes: Penetrating Through Aromatic Armor with the Help of Excited State Antiaromaticity
This review focuses on photocyclization reactions involving alkenes and arenes. Photochemistry opens up synthetic opportunities difficult for thermal methods, using light as a versatile tool to convert stable ground-state molecules into their reactive excited counterparts. This difference can be particularly striking for aromatic molecules, which, according to Baird’s rule, transform from highly stable entities into their antiaromatic “evil twins”. We highlight classical reactions, such as the photocyclization of stilbenes, to show how alkenes and aromatic rings can undergo intramolecular cyclizations to form complex structures. When possible, we explain how antiaromaticity develops in excited states and how this can expand synthetic possibilities. The review also examines how factors such as oxidants, substituents, and reaction conditions influence product selectivity, providing useful insights for improving reaction outcomes and demonstrating how photochemical methods can drive the development of new synthetic strategies
Antiaromaticity Gain Activates Tropone and Nonbenzenoid Aromatics as Normal-Electron-Demand Diels–Alder Dienes
An Unexpected Rearrangement That Disassembles Alkyne Moiety Through Formal Nitrogen Atom Insertion between Two Acetylenic Carbons and Related Cascade Transformations: New Approach to<i>Sampangine</i>Derivatives and Polycyclic Aromatic Amides
An Unexpected Rearrangement That Disassembles Alkyne Moiety Through Formal Nitrogen Atom Insertion between Two Acetylenic Carbons and Related Cascade Transformations: New Approach to Sampangine
Revisiting the Case of an Intramolecular Hydrogen Bond Network Forming Four- and Five-Membered Rings in dGlucose
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