Synfacts, Journal Year: 2022, Volume and Issue: 18(10), P. 1072 - 1072
Published: Sept. 20, 2022
Key words hydroxyalkylation - alcohols nucleosides purines
Language: Английский
Synfacts, Journal Year: 2022, Volume and Issue: 18(10), P. 1072 - 1072
Published: Sept. 20, 2022
Key words hydroxyalkylation - alcohols nucleosides purines
Language: Английский
Science China Chemistry, Journal Year: 2023, Volume and Issue: 66(8), P. 2309 - 2316
Published: July 24, 2023
Language: Английский
Citations
40Chinese Chemical Letters, Journal Year: 2022, Volume and Issue: 34(5), P. 108045 - 108045
Published: Dec. 8, 2022
Language: Английский
Citations
33Chinese Chemical Letters, Journal Year: 2023, Volume and Issue: 35(2), P. 109058 - 109058
Published: Sept. 10, 2023
Language: Английский
Citations
15Chemical Communications, Journal Year: 2024, Volume and Issue: 60(26), P. 3579 - 3582
Published: Jan. 1, 2024
This work reports a one-pot asymmetric synthesis of spirocyclopropyl propionaldehydes/propanols via β,γ-bifunctionalization propanols through the synergistic effect secondary amine catalyst and an oxidant.
Language: Английский
Citations
3Journal of the American Chemical Society, Journal Year: 2024, Volume and Issue: 146(31), P. 21428 - 21441
Published: July 25, 2024
A Minisci-type borylation of unprotected adenosine, adenine nucleotide, and adenosine analogues was successfully achieved through photocatalysis or thermal activation. Despite the challenges posed by presence two potential reactive sites (C
Language: Английский
Citations
3European Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 27(17)
Published: March 11, 2024
Abstract Molecules containing ether skeletons are widely present in drugs, natural products, functional materials, and life science. Direct C(sp 3 )−H bond functionalization is considered a powerful strategy for the construction of novel derivatives. Photo‐/electro‐chemical technology relatively green sustainable synthesis method, which opens up broad application prospect field direct bonds. In recent years, photo‐/electro‐mediated alkylation, arylation, alkynylation, esterification, mercaptoylation, sulfidation, amination ethers have been extensively studied. this review, research progress compounds from 2014 to 2023 systematically reviewed, scope, limitations, mechanisms some reactions discussed.
Language: Английский
Citations
2Chemical Communications, Journal Year: 2023, Volume and Issue: 59(26), P. 3910 - 3913
Published: Jan. 1, 2023
A protocol for visible-light-induced C-H acylation selectively at the C6 position of purine nucleosides with aldehydes under photocatalyst-free conditions was established herein. This allows green, mild, and efficient functionalization various a broad range alkyl aryl aldehydes.
Language: Английский
Citations
6Organic & Biomolecular Chemistry, Journal Year: 2023, Volume and Issue: 21(43), P. 8744 - 8748
Published: Jan. 1, 2023
A halotrimethylsilane facilitated cycloketonization of γ -hydroxyl ynones is detailed for one-step synthesis polysubstituted 3(2 H )-furanone products.
Language: Английский
Citations
6Organic Chemistry Frontiers, Journal Year: 2023, Volume and Issue: 10(13), P. 3313 - 3320
Published: Jan. 1, 2023
A novel light induced 8-endo sulfonyl cyclization to medium-sized benzo[ b ]azocines is developed. DFT calculations rationalize the rate-determining step and chemoselectivity observed in this transformation.
Language: Английский
Citations
5Organic Letters, Journal Year: 2023, Volume and Issue: 25(48), P. 8716 - 8721
Published: Nov. 22, 2023
2-Azidoimines are versatile precursors to value-added vicinal unsymmetrical diamines, which among the most common motifs in biologically active compounds. Herein, we report their operationally simple synthesis through a highly regioselective intermolecular azidoamination of olefins under metal-free conditions. The approach proceeded azide and iminyl, two differentiated N-centered radicals. synthetic potential protocols was further established via condensation/amination sequential cascade chemoselective, orthogonal transformations access primary diamines.
Language: Английский
Citations
5