Results 101 to 110 of about 23,273 (217)

Catalytic enantioselective synthesis of quaternary carbon stereocentres. [PDF]

, 2014
Quaternary carbon stereocentres-carbon atoms to which four distinct carbon substituents are attached-are common features of molecules found in nature. However, before recent advances in chemical catalysis, there were few methods of constructing single ...
Overman, Larry E, Quasdorf, Kyle W
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Ruthenium-catalyzed azide alkyne cycloaddition reaction: scope, mechanism and applications [PDF]

, 2016
The ruthenium-catalyzed azide alkyne cycloaddition (RuAAC) affords 1,5-disubstituted 1,2,3-triazoles in one step and complements the more established copper-catalyzed reaction providing the 1,4-isomer.
Akimova G., Akimova G., Akimova G., Anna Said Stålsmeden, Bader R. F. W., Chandrasekaran S., Das R., Fan W.-Q., Fokin V. V., Gruchlik A., Huisgen R., Johan R. Johansson, Keicher T., Levin J. I., Murahashi S.-I., Neumajer G., Nina Kann, Palaniraja J., Parsons J. G., Schilling C., Tamás Beke-Somfai, Trabocchi A., Yubo J., Zhou Y. B.   +23 more
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Coinage Metal Complexes as Chiral Catalysts for 1,3-Dipolar Cycloadditions [PDF]

, 2014
In this account, we describe the experience of our research group in the implementation of chiral coinage metal complexes into the efficient enantioselective 1,3-DC of azomethine ylides derived from α-amino acids and azlactones with different ...
Nájera, Carmen, Sansano, Jose M.
core   +2 more sources

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

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

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

Enantioselective Total Synthesis of (—)-Acetylaranotin, a Dihydrooxepine Epidithiodiketopiperazine [PDF]

, 2012
The first total synthesis of the dihydrooxepine-containing epidithiodiketopiperazine (ETP) (−)-acetylaranotin (1) is reported. The key steps of the synthesis include an enantioselective azomethine ylide (1,3)-dipolar cycloaddition reaction to set the ...
Codelli, Julian A., Puchlopek, Angela L. A., Reisman, Sarah E.   +2 more
core   +1 more source

Synthesis of new triazole-based trifluoromethyl scaffolds

Beilstein Journal of Organic Chemistry, 2008
Trifluoromethyl propargylamines react with various azide derivatives to afford 1,4-disubstituted 1,2,3-triazoles through a Huisgen 1,3-dipolar cycloaddition. The reaction is catalyzed by a Cu(I) species in acetonitrile, and the corresponding products are
Michela Martinelli, Thierry Milcent, Sandrine Ongeri, Benoit Crousse   +3 more
doaj   +1 more source

Catalytic asymmetric synthesis of highly substituted pyrrolizidines [PDF]

, 2012
A catalytic asymmetric double (1,3)-dipolar cycloaddition reaction has been developed. Using a chiral silver catalyst, enantioenriched pyrrolizidines can be prepared in one flask from inexpensive, commercially available starting materials.
Codelli, Julian A., Lim, Andrew D., Reisman, Sarah E.   +2 more
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