Electrochemical Activation of Bicyclo[1.1.0]butanes. [PDF]
Maddigan-Wyatt JT, Knyazev DA, Werz DB.
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Photochemical Fluoroalkylations with Fluorinated Gases Facilitated by a Robust Metal-Organic Framework. [PDF]
He J +9 more
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Enantioselective synthesis of 1,2-disubstituted thiocyclobutanes <i>via</i> Michael addition. [PDF]
Robert EGL, Waser J.
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Author Correction: Organocatalytic enantioselective [2π + 2σ] cycloaddition reactions of bicyclo[1.1.0]butanes with α,β-unsaturated aldehydes. [PDF]
Geng YX +6 more
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The addition of aldehyde enamines to nitroalkenes affords cyclobutanes in all solvents, with all of the pyrrolidine and proline derivatives tested by us and with all of the substrates we have examined. Depending on the temperature, concentration of water,
Castro Álvarez, Alejandro +5 more
core
Difunctionalization of bicyclo[1.1.0]butanes enabled by merging C-C cleavage and ruthenium-catalysed remote C-H activation. [PDF]
Chen S +4 more
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Diastereoselective 1,3-nitrooxygenation of bicyclo[1.1.0]butanes. [PDF]
Maity A +3 more
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Weight loss at a cost: A case of sibutramine-induced psychotic disorder. [PDF]
Raj K, Au TY, Jacob S, Kour J.
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A General Approach for Strained Ring Functionalization via Nucleophilic Catalysis. [PDF]
Wang P +7 more
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Lewis Acid-Catalyzed Divergent (4+3)/(4+2) Annulations of o-Quinone Methides with Bicyclo[1.1.0]butanes Lead to sp3-Rich Oxabicyclic Frameworks. [PDF]
Mondal S +4 more
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