Results 131 to 140 of about 5,840 (188)
Direct Organocatalytic Chemoselective Synthesis of Pharmaceutically Active 1,2,3-Triazoles and 4,5'-Bitriazoles. [PDF]
Gorachand B +2 more
europepmc +1 more source
Synthetic Strategies to Access Fluorinated Azoles. [PDF]
El-Gaber MKA +4 more
europepmc +1 more source
Radical-Mediated Trifunctionalization Reactions. [PDF]
Zhang Q, Ma X, Zhi S, Zhang W.
europepmc +1 more source
Easy ROMP of Quinine Derivatives Toward Novel Chiral Polymers That Discriminate Mandelic Acid Enantiomers. [PDF]
Majchrzak M +4 more
europepmc +1 more source
Enantioselective Preparation of (<i>N</i>,<i>O</i>)-, (<i>N</i>,<i>N</i>)- and (<i>N</i>,<i>S</i>)-Spiroketal Moieties. [PDF]
Sow M, Fauran E, Commeiras L.
europepmc +1 more source
Electrochemical cyclization of alkynes to construct five-membered nitrogen-heterocyclic rings. [PDF]
Peng L +10 more
europepmc +1 more source
Lewis acid-mediated transformations of 5-acyl-N-fluoroalkyl-1,2,3-triazoles to cyclopentenones, indenones, or oxazoles. [PDF]
Janecký L, Beier P.
europepmc +1 more source
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Angewandte Chemie International Edition in English, 1975
AbstractThis review is designed to demonstrate the versatility of vinyl azides in organic reactions. The reactive azide function is susceptible to thermolysis, photolysis, cycloadditions, and attack by nucleophiles and electrophiles. The neighboring double bond accentuates the reactivity of the azide function and provides additional intramolecular ...
openaire +3 more sources
AbstractThis review is designed to demonstrate the versatility of vinyl azides in organic reactions. The reactive azide function is susceptible to thermolysis, photolysis, cycloadditions, and attack by nucleophiles and electrophiles. The neighboring double bond accentuates the reactivity of the azide function and provides additional intramolecular ...
openaire +3 more sources

