Results 11 to 20 of about 2,936 (205)
Stereoselective synthesis of cyclobutanes by contraction of pyrrolidines [PDF]
Here we report a contractive synthesis of multisubstituted cyclobutanes containing multiple stereocenters from readily accessible pyrrolidines using iodonitrene chemistry.
Brieger, L +7 more
core +2 more sources
Preparation of cyclobutanes with four different substituents is rare and often arduous. Here a cocrystallisation strategy enables the intermolecular [2+2] cross-photoreaction of non-symmetrical stilbene derivatives to obtain chiral tetrasubstituted ...
Michael A. Sinnwell +4 more
doaj +1 more source
The Synthesis of Functionalized Dimethylphosphinoyl Cyclopropanes and Cyclobutanes
A simple preparative approach to a series of functionalized dimethylphosphinoyl-containing cyclopropanes and cyclobutanes has been developed; it is based on cyclocondensation of dimethylphosphinoyl acetonitrile with 1,2- and 1,3-dibromoalkanes. Synthetic
Anastasiia M. Aleksandrova +2 more
doaj +1 more source
Skeletal contraction: A novel strategy to access multisubstituted cyclobutane
The polysubstituted and spirocyclic cyclobutanes were efficiently constructed by the utilization of a novel skeletal contraction strategy which only took one-step synthesis from the readily accessible pyrrolidines.
Chunfa Xu +2 more
doaj +1 more source
The stereoselective synthesis of cyclobutanes that possess an array of stereocenters in a contiguous fashion has attracted the wide interest of the synthetic community.
Roger Monreal-Corona (14818063) +3 more
core +2 more sources
Radical cation Diels–Alder reactions of arylidene cycloalkanes
TiO2 photoelectrochemical and electrochemical radical cation Diels–Alder reactions of arylidene cycloalkanes are described, leading to the construction of spiro ring systems.
Kaii Nakayama +2 more
doaj +1 more source
NMR and Computational Studies on the Reactions of Enamines with Nitroalkenes That May Pass through Cyclobutanes [PDF]
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,
Alejandro Castro-Alvarez +5 more
doaj +3 more sources
Light-induced [2 + 2] cycloaddition is the most efficient way to generate cyclobutanes, while suffering from limitations of specific selectivity.
Jing-Si Wang +8 more
doaj +1 more source
Contemporary synthesis of bioactive cyclobutane natural products
Many cyclobutane natural products have intriguing biological properties that arise from their fascinating chemical structures. Cyclobutane natural products feature a cyclobutane scaffold as the core or as a part of the spirocyclic or fused cyclic core ...
Chunngai Hui +3 more
doaj +1 more source
While polyborylated alkenes are being recognized for their elevated status as highly valuable reagents in modern organic synthesis, allowing efficient access to a diverse array of transformations, including the formation of C–C and C–heteroatom bonds ...
Nicole, Hanania +2 more
core +1 more source

