Results 101 to 110 of about 16,669 (224)

Synthesis of oxetane/azetidine containing spirocycles via the 1,3-dipolar cycloaddition reaction [PDF]

, 2016
Silver catalyzed 1,3-dipolar cycloaddition reactions between methyl 2-(oxetane/azetidine-3 ylidene) acetate as dipolarophiles and imines derived from –amino acid methyl esters, 2-aminomethyl pyridine and 2-aminomethyl pyrazine afforded oxetane/azetidine ...
Proud, M, Jones, B, Sridharan, V
core   +1 more source

Alkylation and 1,3-Dipolar Cycloaddition of 6-Styryl-4,5-dihydro-2H-pyridazin-3-one: Synthesis of Novel N-Substituted Pyridazinones and Triazolo[4,3-b]pyridazinones

Journal of Chemistry, 2013
Some new N-substituted pyridazinones and triazolo[4,3-b]pyridazinones were synthesized, respectively, by simple alkylation and 1,3-dipolar cycloaddition of pyridazin-3-one with nitrile imines.
Souad Mojahidi, Hanan Sekkak, El Mostapha Rakib, Maria G. P. M. S. Neves, Maria A. F. Faustino, José A. S. Cavaleiro, Hafid Zouihri   +6 more
doaj   +1 more source

Crystal structure of (2R*,3aR*)-2-phenylsulfonyl-2,3,3a,4,5,6-hexahydropyrrolo[1,2-b]isoxazole

Acta Crystallographica Section E: Crystallographic Communications, 2017
The title compound, C12H15NO3S, was prepared by 1,3-dipolar cycloaddition of 3,4-dihydro-2H-pyrrole 1-oxide and phenyl vinyl sulfone. In the molecule, both fused five-membered rings display a twisted conformation.
Yaiza Hernández, Isidro Marcos, Narciso M. Garrido, Francisca Sanz, David Diez   +4 more
doaj   +1 more source

Synthesis and Characterization of some New Mesoionic 1,3-Thiazolium-5-thiolates via Cyclodehydration and in situ 1,3-Dipolar Cycloaddition/Cycloreversion

Molecules, 2002
The title compounds were synthesized from C-aryl-N-methylglycines by Naroylation followed by a cyclodehydration to form the corresponding 1,3-oxazolium-5-olates.
Maria Joaquina Vieira, Aderson de Farias Dias, Alfredo Mayall Simas, Joseph Miller, Petrônio Filgueiras de Athayde Filho, Bruno Freitas Lira   +5 more
doaj   +1 more source

CUCURBITURIL-INDUCED 1,3-DIPOLAR CYCLOADDITION.

, 1986
CUCURBITURIL-INDUCED 1,3-DIPOLAR ...
MITA. ADHYA (7978196)
core  

Chemical Structure Data File For K. Zong's Thesis, "The 1,3-dipolar cycloaddition of nitrile oxides to vinylboronic esters and asymmetric approaches."

, 2020
This Structure Data File (SDfile) is associated with the thesis: Zong, K. "The 1,3-dipolar cycloaddition of nitrile oxides to vinylboronic esters and asymmetric approaches." and http://library.ua.edu/vwebv/holdingsInfo?bibId=851312 It is distributed by ...
Scalfani, Vincent F.
core  

Diethyl 4-acetyl-5-(2-nitrophenyl)pyrrolidine-2,2-dicarboxylate

Acta Crystallographica Section E, 2010
The title compound, C18H22N2O7, was synthesized by the 1,3-dipolar cycloaddition reaction of but-3-en-2-one, diethyl 2-aminomalonate and 2-nitrobenzaldehyde. In the molecule, the pyrrolidine ring possesses an envelope conformation.
Long He
doaj   +1 more source

One-flask synthesis of 1,3,5-trisubstituted 1,2,4- triazoles from nitriles and hydrazonoyl chlorides via 1,3-dipolar cycloaddition

, 2014
[[abstract]]A new “one-flask” synthesis of 3,5-disubstituted 1,2,4-triazoles has successfully been developed to synthesize a series of 3,5-disubstituted 1,2,4-triazoles.
Wang, Li-Ya;Wang, Li-Ya;蔡建鈞;Tsai, Henry J;Lin, Hui-Yi;Lin, Hui-Yi;Ka, Kimiyoshi;Kaneko, Kimiyoshi;Che, Fen-Ying;Cheng, Fen-Ying;Sh, Hsin-Siao;Shih, Hsin-Siao;Won, Fung Fuh;Wong, Fung Fuh;Hu, Jiann-Jyh;Huang, Jiann-Jyh
core  

Highly Regioselective 1,3-Dipolar Cycloaddition of Nitrilimines and Thioaurones Towards Spiro-2-Pyrazolines: Synthesis, Characterization, and Mechanistic Study

Reactions
In this paper, we report a highly regioselective 1,3-dipolar cycloaddition (1,3-DC) reaction of nitrilimines with thioaurone derivatives that afforded the hitherto unreported spiropyrazolines. Spectroscopic and spectrometric data were utilized to confirm
Mohamed Bakhouch, Bouchra Es-Sounni, Ayoub Ouaddi, Khaoula Oudghiri, Mohammed Chalkha, Lahoucine Bahsis, Taoufiq Benali, Mohamed Bourass, Rabiaa Fdil, Mohamed Akhazzane, Mohamed El Yazidi   +10 more
doaj   +1 more source

Synthesis of highly functionalized β-aminocyclopentanecarboxylate stereoisomers by reductive ring opening reaction of isoxazolines

Beilstein Journal of Organic Chemistry, 2012
A rapid and simple procedure was devised for the synthesis of multifunctionalized cyclic β-amino esters and γ-amino alcohols via the 1,3-dipolar cycloaddition of nitrile oxides to β-aminocyclopentenecarboxylates.
Melinda Nonn, Loránd Kiss, Reijo Sillanpää, Ferenc Fülöp   +3 more
doaj   +1 more source