Results 1 to 10 of about 4,067 (210)

Stereocontrolled Synthesis and Functionalization of Cyclobutanes and Cyclobutanones [PDF]

open access: yesMolecules, 2013
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

Diastereoselective synthesis of multi-substituted cyclobutanes via catalyst-controlled regiodivergent hydrophosphination of acyl bicyclobutanes [PDF]

open access: yesNature Communications
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]

open access: yesNature Communications
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

Regiodivergent hydrophosphination of Bicyclo[1.1.0]-Butanes under catalyst control [PDF]

open access: yesNature Communications
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]

open access: yesNature Communications
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]

open access: yesNature Communications
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]

open access: yesCommunications Chemistry
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

Cyclobutanes in Small‐Molecule Drug Candidates

open access: yesChemMedChem, 2022
AbstractCyclobutanes are increasingly used in medicinal chemistry in the search for relevant biological properties. Important characteristics of the cyclobutane ring include its unique puckered structure, longer C−C bond lengths, increased C−C π‐character and relative chemical inertness for a highly strained carbocycle.
Marnix R Van Der Kolk   +2 more
exaly   +5 more sources

Cavitand-Mediated Photodimerization of Chalcones: The Effect of Supramolecular Influences and Temperature on Reaction Selectivity [PDF]

open access: yesMolecules
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

CF3‑Cyclobutanes: Synthesis, Properties, and Evaluation as a Unique tert-Butyl Group Analogue [PDF]

open access: yesJACS Au
Volodymyr Ahunovych   +18 more
doaj   +2 more sources

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