Журнал органической химии, Journal Year: 2024, Volume and Issue: 60(2-3)
Published: Dec. 27, 2024
Language: Английский
Журнал органической химии, Journal Year: 2024, Volume and Issue: 60(2-3)
Published: Dec. 27, 2024
Language: Английский
Russian Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 60(8), P. 1361 - 1584
Published: Aug. 1, 2024
Language: Английский
Citations
6The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 89(7), P. 4496 - 4502
Published: March 20, 2024
Acyl ketenes react with polar unsaturated functional groups to give unique heterocyclic rings, yet reactions unpolarized have not been reported. Herein, we describe two effective ring-forming between acetyl ketene and electron-deficient alkynes. The first reaction involves in situ tethering nucleophile-containing 1,3-diynones, which promotes sequential intramolecular 1,6/1,4-additions generate 2-methylene-2H-pyrans various yields (24–91%). other a zwitterionic intermediate generated from DABCO, undergoes Michael addition terminal alkynyl ketones 3-acyl-4-pyrones (11–79%).
Language: Английский
Citations
4ChemistrySelect, Journal Year: 2025, Volume and Issue: 10(21)
Published: May 30, 2025
Abstract Pyrans are a class of six‐membered heterocyclic rings containing five carbon atoms and one oxygen atom. They non‐aromatic in nature, bearing two double bonds the ring. The bond position distinguishes pyran isomers, namely, 2 H ‐pyran 4 ‐pyran. When saturated sp 3 is located next to an atom, it known as ‐pyran, when at 4‐position with respect In 1962, by thermal breakdown 2‐acetoxy‐3,4‐dihydro‐2 ‐pyrans were produced for first time, their characteristics explored. Numerous synthetic methods have been disclosed over time owing broad applications diverse fields, mainly drug design, pharmaceuticals, material science. this review, we highlight recent advancements toward substituted 4‐pyranone, 2‐pyranones, focusing on reports published from 2019 till date, which play important roles both organic synthesis types functional molecules.
Language: Английский
Citations
0Progress in heterocyclic chemistry, Journal Year: 2024, Volume and Issue: unknown, P. 421 - 484
Published: Jan. 1, 2024
Language: Английский
Citations
0The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: unknown
Published: Nov. 20, 2024
We report herein a concise route for the total synthesis of rapicone. The key strategy to form ynone intermediate involves an Fe(III)/TEMPO-catalyzed aerobic oxidation 1,3-dihydroisobenzofuran moiety. This ether simultaneous installation keto aldehyde allowed effective formation required intermediate. rapicone is substantiated by unique formal [4 + 2] cycloaddition acyl ketene with alkynone and completed in 7 steps 9.4% overall yield.
Language: Английский
Citations
0Журнал органической химии, Journal Year: 2024, Volume and Issue: 60(2-3)
Published: Dec. 27, 2024
Language: Английский
Citations
0