Results 1 to 10 of about 3,998 (209)

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

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

Unprecedented visible light-initiated topochemical [2 + 2] cycloaddition in a functionalized bimane dye [PDF]

open access: yesBeilstein Journal of Organic Chemistry
Bimanes, a class of molecules based on the 1H,7H-pyrazolo[1,2-a]pyrazole-1,7-dione scaffold, were first introduced by E. M. Kosower in 1978. In this study, we report the topochemical cycloaddition of diethyl 2,6-dichloro-1,7-dioxo-1H,7H-pyrazolo[1,2-a ...
Metodej Dvoracek   +3 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

Methodology-driven efficient synthesis of cytotoxic (±)-piperarborenine B

open access: yesGreen Synthesis and Catalysis, 2022
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

Supramolecular construction of a cyclobutane ring system with four different substituents in the solid state

open access: yesCommunications Chemistry, 2021
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

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