About
Contact & Profiles
A5092875812
Research Areas
- Photochemistry and Electron Transfer Studies
- Chemical Reaction Mechanisms
- Catalytic C–H Functionalization Methods
- Organic Chemistry Cycloaddition Reactions
- Porphyrin and Phthalocyanine Chemistry
- Synthesis and Properties of Aromatic Compounds
- Axial and Atropisomeric Chirality Synthesis
- Chemical synthesis and alkaloids
- Photochromic and Fluorescence Chemistry
- Radical Photochemical Reactions
- Sulfur-Based Synthesis Techniques
N.D. Zelinsky Institute of Organic Chemistry
2023-2024
10.1016/j.dyepig.2024.112032
article
EN
Dyes and Pigments
2024-03-02
Abstract A multifaceted study on the effect of various factors efficiency photocyclization naphthofuran O‐acyl oximes was performed. It showed that without any additives or in presence electron acceptors, reaction occurs by a radical pathway and with low chemoselectivity, while DABCO promotes intramolecular cyclization to give naphthofuroquinolines (NFQs) 34–87% yields. The iminyl formed under UV irradiation due single transfer (SET) N−O bond cleavage undergoes selective homolytic aromatic...
10.1002/adsc.202300833
article
EN
Advanced Synthesis & Catalysis
2023-09-16
10.1134/s0018143923090175
article
EN
High Energy Chemistry
2023-12-01
10.2139/ssrn.4930476
preprint
EN
2024-01-01
The [1,2]-aryl shift reaction was used to synthesize naphtho[2,1-
10.1039/d4ob01223b
article
EN
Organic & Biomolecular Chemistry
2024-01-01
10.1016/j.jphotochem.2024.116106
article
EN
Journal of Photochemistry and Photobiology A Chemistry
2024-10-20
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