In this paper we describe an efficient method for the synthesis of new heterocyclic systems: furo[2,3-]-2,7-naphthyridines , as well as a new method for the preparation of 1,3-diamino-2,7-naphthyridines . For the first time, a Smiles rearrangement was carried out in the 2,7-naphthyridine series, thus gaining the opportunity to synthesize 1-amino-3-oxo-2,7-naphthyridines , which are the starting compounds for obtaining furo[2,3-]-2,7-naphthyridines. The cyclization of alkoxyacetamides proceeds via two different processes: the expected formation of furo[2,3-]-2,7-naphthyridines and the 'unexpected' formation of 1,3-diamino-2,7-naphthyridines ( a Smiles type rearrangement).

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9179986PMC
http://dx.doi.org/10.3390/ijms23115904DOI Listing

Publication Analysis

Top Keywords

smiles rearrangement
8
synthesis 1-amino-3-oxo-27-naphthyridines
4
1-amino-3-oxo-27-naphthyridines smiles
4
rearrangement approach
4
approach field
4
field chemistry
4
chemistry heterocyclic
4
heterocyclic compounds
4
compounds paper
4
paper describe
4

Similar Publications

Succinyldiamide derivatives are important structural motifs in various natural products, pharmaceuticals, and functional materials. Herein, a novel, mild, and environmentally friendly method was developed for synthesizing functionalized succinyldiamides each containing a quaternary carbon center. This strategy was designed to involve photocatalytic decarboxylation of readily available oxalic monoamide using a non-precious metal photocatalyst, 4CzIPN, followed by a free-radical addition/Smiles rearrangement cascade reaction of -aryl--(arylsulfonyl)acrylamides.

View Article and Find Full Text PDF

Photoredox Radical Truce-Smiles Rearrangement of Sulfinyl Acrylamides with Bromodifluoroacetamides.

Org Lett

December 2024

Key Laboratory of Environmentally Friendly Chemistry and Application of Ministry of Education, College of Chemistry, Xiangtan University, Xiangtan, Hunan 411105, China.

We herein report a photochemical Truce-Smiles rearrangement reaction of -sulfinyl acrylamides with bromodifluoroacetamides resulting in the synthesis of a series of aryl difluoroglutaramides in moderate to good yields. The asymmetric synthesis using chiral sulfinamides produced quaternary carboncentered glutaramide products with a modest enantioselectivity. This protocol effectively complements previous Truce-Smiles rearrangement methods involving -sulfonyl acrylamides.

View Article and Find Full Text PDF

Cysteine (Cys) plays a critical role in various biological processes, including protein synthesis, cellular signaling, and antioxidant defense. However, precise detection of Cys in biological systems remains challenging due to interference from similar thiols such as homocysteine (Hcy) and glutathione (GSH). In this study, we report the synthesis and bioimaging of a novel ratio-type fluorescent probe based on the benzoBODIPY fluorophore, designed for the ratiometric detection of Cys.

View Article and Find Full Text PDF

Photocyclization of 8-aryloxy-3-phenylbenzo[][1,2,4]triazines leads to π-delocalized helicene radicals 1[n] ( = 5, 6, 7) containing the ring-fused 1,4-dihydro[1,2,4]triazin-4-yl as a spin source. Single crystal XRD revealed that the photocyclization to 1[n] involves a Smiles rearrangement. Radicals 1[n] were investigated by spectroscopic, electrochemical and DFT methods, while racemic helicene 1[7] was resolved and ECD spectra were recorded.

View Article and Find Full Text PDF

Iron-Catalyzed SO-Retaining Smiles Rearrangement through Decarboxylation.

Org Lett

December 2024

Institute of Green Chemistry and Molecular Engineering, GBRCE for Functional Molecular Engineering, Lehn Institute of Functional Materials, School of Chemistry, Sun Yat-sen University, Guangzhou 510006, PR China.

Radical Smiles rearrangements have emerged as powerful methodologies for constructing carbon-carbon bonds through intramolecular radical addition and fragmentation under milder conditions, with SO released as a byproduct. However, SO-retaining Smiles rearrangements, which can yield valuable alkyl sulfone derivatives, have been scarcely explored. In this study, we present an unprecedented iron-catalyzed SO-retaining Smiles rearrangement initiated by the decarboxylation of aliphatic carboxylic acids.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!