The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: unknown
Published: Nov. 12, 2024
A visible-light-promoted protocol for azaspirocyclic synthesis from
Language: Английский
The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: unknown
Published: Nov. 12, 2024
A visible-light-promoted protocol for azaspirocyclic synthesis from
Language: Английский
The Journal of Organic Chemistry, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 14, 2025
Visible-light-driven metal- and photocatalyst-free cascade 1,4-HAT dearomative spirocyclization of N-benzylacrylamides are described for sustainable synthesis a variety pharmaceutically important γ-ketoamides 2-Azaspiro[4.5]decanes in one pot good to excellent yields. Readily accessible nontoxic materials, expensive Ir or Ru mild conditions, functional group tolerance, operational simplicity, scalability enhance the practical value this protocol. Mechanistic studies reveal that acyl radicals generated from α-oxocarboxylic acids trigger rare spirocyclization. The synthetic potential environmentally benign method is further showcased by late-stage functionalization drug molecules, amino acid, peptides.
Language: Английский
Citations
0Tetrahedron Letters, Journal Year: 2025, Volume and Issue: unknown, P. 155629 - 155629
Published: May 1, 2025
Language: Английский
Citations
0Colloids and Surfaces B Biointerfaces, Journal Year: 2023, Volume and Issue: 234, P. 113720 - 113720
Published: Dec. 21, 2023
Language: Английский
Citations
8Organic & Biomolecular Chemistry, Journal Year: 2024, Volume and Issue: 22(30), P. 6141 - 6148
Published: Jan. 1, 2024
Construction of seleno azaspiro[4.5]decadienones using an electrochemical approach is achieved via domino selenylation/ ipso -annulation.
Language: Английский
Citations
2European Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 27(31)
Published: June 6, 2024
Abstract An efficient method for the conversion of biphenyl acrylamides to dibenzoazepinones with −SCF 3 incorporation is described. This operationally simple radical cascade reaction employs CAN as an oxidant and exhibits good functional group tolerance. Substrates featuring −OCH , −CH −Br or −Cl at para ‐position aromatic ring a preference ipso ‐cyclization due intervention DMSO in reaction. Density theory (DFT) calculations provide valuable insights into reaction's energetics product selectivity.
Language: Английский
Citations
1Organic Chemistry Frontiers, Journal Year: 2024, Volume and Issue: 11(23), P. 6850 - 6917
Published: Jan. 1, 2024
In this review, we summarize the latest developments and applications of Mn(OAc) 3 in organic synthesis over past decade, focusing on efforts to achieve milder reaction conditions while expanding scope possibilities.
Language: Английский
Citations
0The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: unknown
Published: Nov. 12, 2024
A visible-light-promoted protocol for azaspirocyclic synthesis from
Language: Английский
Citations
0