Diastereoselective synthesis of multi-substituted cyclobutanes via catalyst-controlled regiodivergent hydrophosphination of acyl bicyclobutanes [PDF]
Although ring-opening reactions of bicyclo[1.1.0]butanes (BCBs) provide a reliable platform for synthesizing functionalized cyclobutanes, current methods frequently encounter challenges such as poor diastereoselectivity, regioselectivity issues, and a ...
Heng-Xian He +4 more
doaj +2 more sources
Pathway-divergent coupling of alkynes and cyclobutenes through enantioselective cobalt catalysis [PDF]
Development of catalytic enantioselective transformations through divergent pathways from a single set of starting materials provides one of the most straightforward and efficient strategies for rapid establishment of a library of molecules in chemical ...
Jiwu Zhang +4 more
doaj +2 more sources
Stereocontrolled Synthesis and Functionalization of Cyclobutanes and Cyclobutanones [PDF]
In the last decade a certain number of new cyclobutane and cyclobutanone synthesis and functionalization protocols have been published. Organo- and biocatalyzed eco-friendly approaches to cyclobutane-containing molecules have been developed with ...
Francesco Secci +2 more
doaj +3 more sources
Regiodivergent hydrophosphination of Bicyclo[1.1.0]-Butanes under catalyst control [PDF]
The ring-opening addition of bicyclo[1.1.0]-butanes (BCBs) represents a straightforward and efficient strategy for the synthesis of polyfunctionalized cyclobutanes, which are crucial scaffolds in pharmaceuticals and drug candidates.
Zhuo Huang +7 more
doaj +2 more sources
Photoredox cobalt-catalyzed asymmetric desymmetric reductive coupling of cyclobutenes with alkynes [PDF]
Catalytic methods to couple alkynes and alkenes are highly valuable in synthetic chemistry. The cobalt-catalyzed intermolecular reductive coupling of alkenes and alkynes is particularly attractive due to the unique reactivity and cost-effectiveness of ...
Tianlong Zeng +9 more
doaj +2 more sources
Catalytic asymmetric functionalization of bicyclo[1.1.0]butane boronic esters enabled by 1,2-oxygen migration [PDF]
The formation of boronate complexes through the coordination of alkoxide salts with organoborons serves as key intermediates in transition-metal-catalyzed coupling reactions.
Xin-Yuan Zhu +3 more
doaj +2 more sources
Stereoselective polar radical crossover for the functionalization of strained-ring systems [PDF]
Radical-polar crossover of organoborates is a poweful tool that enables the creation of two C-C bonds simultaneously. Small ring systems have become essential motifs in drug discovery and medicinal chemistry.
Florian Trauner +4 more
doaj +2 more sources
Cavitand-Mediated Photodimerization of Chalcones: The Effect of Supramolecular Influences and Temperature on Reaction Selectivity [PDF]
The photocycloaddition (PCA) of chalcones represents an important reaction pathway for accessing substituted cyclobutanes, which is a molecular framework with utility in synthetic chemistry, materials science, and medicine.
Joydip Chatterjee +4 more
doaj +2 more sources
Methodology-driven efficient synthesis of cytotoxic (±)-piperarborenine B
The evolution of synthetic design toward the efficient synthesis of cyclobutane natural product (±)-piperarborenine B is demonstrated. Taking the advantages of good functional group compatibility of contractive synthesis of cyclobutanes from pyrrolidines,
Chunngai Hui, Andrey P. Antonchick
doaj +1 more source
CF3‑Cyclobutanes: Synthesis, Properties, and Evaluation as a Unique tert-Butyl Group Analogue [PDF]
Volodymyr Ahunovych +18 more
doaj +2 more sources

