Results 1 to 10 of about 107 (106)

Light-induced synthesis of 2H-azirines and its applications in organic chemistry

Journal of Saudi Chemical Society
2H-azirines have represented versatile building motifs in the domain of organic chemistry owing to their excellent reaction activity induced by the high strain of the three-membered ring species.
Yiwen Chu, Junfeng Deng
exaly   +3 more sources

2H-Azirines as dipolarophiles [PDF]

Tetrahedron Letters, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
Melo, Teresa M. V. D. Pinho e, Cardoso, Ana L., Gomes, Clara S. B., Gonsalves, António M. d'A. Rocha   +3 more
openaire   +2 more sources

Copper(II)-Catalyzed (3+2) Cycloaddition of 2H-Azirines to Six-Membered Cyclic Enols as a Route to Pyrrolo[3,2-c]quinolone, Chromeno[3,4-b]pyrrole, and Naphtho[1,8-ef]indole Scaffolds

Molecules, 2022
A method for the [2+3] pyrroline annulation to the six-membered non-aromatic enols using 3-aryl-2H-azirines as annulation agents is developed in the current study.
Pavel A. Sakharov, Nikolai V. Rostovskii, Alexander F. Khlebnikov, Mikhail S. Novikov   +3 more
doaj   +1 more source

Triethylamine-Promoted Oxidative Cyclodimerization of 2H-Azirine-2-carboxylates to Pyrimidine-4,6-dicarboxylates: Experimental and DFT Study

Molecules, 2023
An unprecedented oxidative cyclodimerization reaction of 2H-azirine-2-carboxylates to pyrimidine-4,6-dicarboxylates under heating with triethylamine in air is described. In this reaction, one azirine molecule undergoes formal cleavage across the C-C bond
Timofei N. Zakharov, Pavel A. Sakharov, Mikhail S. Novikov, Alexander F. Khlebnikov, Nikolai V. Rostovskii   +4 more
doaj   +1 more source

5-Chloroisoxazoles: A Versatile Starting Material for the Preparation of Amides, Anhydrides, Esters, and Thioesters of 2H-Azirine-2-carboxylic Acids

Molecules, 2022
Amides, anhydrides, esters, and thioesters of 2H-azirine-2-carboxylic acids were prepared by a rapid procedure at room temperature involving FeCl2-catalyzed isomerization of 5-chloroisoxazoles to 2H-azirine-2-carbonyl chlorides, followed by reaction with
Anastasiya V. Agafonova, Mikhail S. Novikov, Alexander F. Khlebnikov   +2 more
doaj   +1 more source

Organo-photocatalytic Synthesis of Functionalized Pyrroles from 2H-Azirines and α-Substituted Nitroalkenes

SynOpen, 2022
An efficient organo-photocatalytic method for the synthesis of tetrasubstituted pyrroles bearing a ketone, ester, alcohol, or nitro group at the 3-position has been developed.
Lalita Devi, Poornima Mishra, Ayushi Pokhriyal, Namrata Rastogi   +3 more
doaj   +1 more source

Azirine alkylation

Tetrahedron Letters, 1976
Tetrahedron Letters 17 (1976) 1413-1414. doi:10.1016/S0040-4039(00)71270-6 ; Received by publisher: 1975-12-23 ; Harvest Date: 2016-01-04 12:20:50 ; DOI:10.1016/S0040-4039(00)71270-6 ; Page Range: 1413 ...
Department of Chemistry, University of Florida Gainesville, Florida 32611 U.S.A. ( host institution ), Deyrup, James A. ( author ), Szabo, William A. ( author )   +2 more
openaire   +2 more sources

[3 + 2]-Cycloadditions of nitrile ylides after photoactivation of vinyl azides under flow conditions

Beilstein Journal of Organic Chemistry, 2013
The photodenitrogenation of vinyl azides to 2H-azirines by using a photoflow reactor is reported and compared with thermal formation of 2H-azirines. Photochemically, the ring of the 2H-azirines was opened to yield the nitrile ylides, which underwent a [3
Stephan Cludius-Brandt, Lukas Kupracz, Andreas Kirschning   +2 more
doaj   +1 more source

Azirine ligation: fast and selective protein conjugation via photoinduced azirine–alkene cycloaddition [PDF]

Chemical Communications, 2010
We report a new bioorthogonal ligation reaction between p-nitrodiphenylazirine and dimethyl fumarate. This photoinduced azirine-alkene cycloaddition provides a rapid (~2 min) and highly selective route to protein conjugation at neutral pH and room temperature in biological medium.
Reyna K V, Lim, Qing, Lin
openaire   +2 more sources

Copper(I)-catalyzed asymmetric decarboxylative Mannich reaction enabled by acidic activation of 2H-azirines

Nature Communications, 2019
Due to their poor electrophilicity, 2H-azirines do not easily react with nucleophiles. Here, the authors show an acidic activation of 2H-azirines by cyanoacetic acid coupling partners affording chiral aziridines containing vicinal tetrasubstituted and ...
Hai-Jun Zhang, Yan-Cheng Xie, Liang Yin
doaj   +1 more source