Recent advances in tandem selenocyclization and tellurocyclization with alkenes and alkynes
K Sun, X Wang, C Li, H Wang, L Li - Organic Chemistry Frontiers, 2020 - pubs.rsc.org
Seleno-containing heterocycles exist widely in pharmaceutical molecules and the skeletons
of natural products. The addition of organoselenium to alkenes and alkynes via …
of natural products. The addition of organoselenium to alkenes and alkynes via …
Synthesis of Seleno‐Heterocycles via Electrophilic/Radical Cyclization of Alkyne Containing Heteroatoms
AD Sonawane, RA Sonawane… - Advanced Synthesis …, 2020 - Wiley Online Library
Abstract containing heterocyclic scaffolds by virtue of their interesting reactivities and a
broad range of applications in the medicinal and materials chemistry. This review involves …
broad range of applications in the medicinal and materials chemistry. This review involves …
Diorganyl diselenides: a powerful tool for the construction of selenium containing scaffolds
AD Sonawane, RA Sonawane, M Ninomiya… - Dalton …, 2021 - pubs.rsc.org
Organoselenium compounds find versatile applications in organic synthesis, materials
synthesis, and ligand chemistry. Organoselenium heterocycles are widely studied agents …
synthesis, and ligand chemistry. Organoselenium heterocycles are widely studied agents …
Recent Developments in Selenylation of Alkynes
Y Xu, D Huang, J Wu, X Wu - Advanced Synthesis & Catalysis, 2024 - Wiley Online Library
Alkynes are simple yet important organic feedstocks. The selenylation of alkynes is able to
produce complex selenium‐containing compounds in a facile way. Although there are some …
produce complex selenium‐containing compounds in a facile way. Although there are some …
Iodine pentoxide-mediated oxidative selenation and seleno/thiocyanation of electron-rich arenes
YH Wang, YQ Zhang, CF Zhou, YQ Jiang… - Organic & …, 2022 - pubs.rsc.org
A simple and efficient method for the regioselective selenation of electron-rich arenes by
employing non-metal inorganic iodine pentoxide (I2O5) as a reaction promoter under …
employing non-metal inorganic iodine pentoxide (I2O5) as a reaction promoter under …
Stereoselective Reduction of Alkynes: Synthesis of 4-Organoselenyl Quinolines
G Lutz, JTK Jung, DF Back… - The Journal of Organic …, 2022 - ACS Publications
This study describes the reaction of 2-amino arylalkynyl ketones with organoselenolates to
form (Z)-vinyl selenides, which lead to 4-organoselenyl quinolines via an intramolecular …
form (Z)-vinyl selenides, which lead to 4-organoselenyl quinolines via an intramolecular …
Transition Metal‐Free Synthesis of Carbo‐and Heterocycles via Reaction of Alkynes with Organylchalcogenides
This manuscript intends to overview the most recent advances in the synthesis of carbo‐and
heterocycles through reactions of alkynes with organyl chalcogenides (S, Se, Te) under …
heterocycles through reactions of alkynes with organyl chalcogenides (S, Se, Te) under …
Synthesis and photophysical properties of selenopheno [2, 3-b] quinoxaline and selenopheno [2, 3-b] pyrazine heteroacenes
AD Sonawane, A Shimozuma, T Udagawa… - Organic & …, 2020 - pubs.rsc.org
In this paper, we report the novel synthesis of three different heterocycles, namely 2-
arylselenopheno [2, 3-b] quinoxaline, 3-(aryl/alkylselanyl)-2-arylselenopheno [2, 3-b] …
arylselenopheno [2, 3-b] quinoxaline, 3-(aryl/alkylselanyl)-2-arylselenopheno [2, 3-b] …
Palladium-Catalyzed Cascade 5-endo-dig Cyclization of Ynamides to Form 4-Alkynyloxazolones
TAC Goulart, DF Back, S Moura E. Silva… - The Journal of Organic …, 2022 - ACS Publications
The selective synthesis of 4-alkynyloxazolones and their further applications as substrates to
electrophile-promoted nucleophilic cyclization have been developed. The reaction of …
electrophile-promoted nucleophilic cyclization have been developed. The reaction of …
Exploration of Synthetic Potential of Quinoline‐3‐Carbaldehydes
Quinoline is one of the most important nitrogen containing heterocycles, being widespread
in nature and present in a broad variety of pharmacologically active compounds …
in nature and present in a broad variety of pharmacologically active compounds …