Results 1 to 10 of about 14,677 (287)

4,5-Dihydro-2H-pyridazin-3-ones as a Platform for the Construction of Chiral 4,4-Disubstituted-dihydropyridazin-3-ones [PDF]

open access: yesMolecules
4,5-Dihydro-2H-pyridazin-3-ones (DHPDOs) are important synthetic as well as naturally occurring heterocycles. We herein report the synthesis of various 4-monofunctionalized 4,5-dihydro-2H-pyridazin-3-ones and their use as starting materials to access 4,4-
Paul Joël Henry   +4 more
doaj   +2 more sources

Site- and enantioselective B−H functionalization of carboranes [PDF]

open access: yesNature Communications
Functionalization of carboranes, icosahedral boron−carbon molecular clusters, is of great interest as they have wide applications in medicinal and materials chemistry.
Kyungsup Lee   +9 more
doaj   +2 more sources

Stereospecific Construction of Quaternary Carbon Stereocenters from Quaternary Carbon Stereocenters

open access: yesJournal of the American Chemical Society, 2022
Organoaluminum species promote a smooth nucleophilic substitution at the quaternary carbon stereocenter of stereodefined polysubstituted cyclopropyl methyl phosphate with a complete inversion of configuration, even when more reactive functional groups are present. The regio- and diastereoselectivity of the substitution is attributed to the existence of
Patel, Kaushalendra   +2 more
openaire   +2 more sources

Regio- and enantioselective umpolung gem-difluoroallylation of hydrazones via palladium catalysis enabled by N-heterocyclic carbene ligand

open access: yesNature Communications, 2021
Installation of difluoroalkyl groups while also imparting stereochemical information is mostly only possible with organocatalytic methods that activate carbonyls.
Shuai Huang   +11 more
doaj   +1 more source

A concise access to bridged [2,2,1] bicyclic lactones with a quaternary stereocenter via stereospecific hydroformylation

open access: yesNature Communications, 2021
Enantiomeric bridged [2,2,1] bicyclic lactone skeletons and their ring-opening products are important scaffolds widely occurring in both pharmaceutics and biology active compounds.
Shuailong Li   +5 more
doaj   +1 more source

Structural basis of the stereoselective formation of the spirooxindole ring in the biosynthesis of citrinadins

open access: yesNature Communications, 2021
Prenylated indole alkaloids contain spirooxindole rings with a 3R or 3S carbon stereocenter, which determines their bioactivities, but the biocatalytic mechanism controlling the 3R- or 3S-spirooxindole formation was unclear.
Zhiwen Liu   +12 more
doaj   +1 more source

Nickel-Catalyzed Removal of Alkene Protecting Group of Phenols, Alcohols via Chain Walking Process

open access: yesMolecules, 2020
An efficient nickel-catalyzed removal of alkene protection group under mild condition with high functional group tolerance through chain walking process has been established.
Chenkai Meng   +4 more
doaj   +1 more source

The Design, Synthesis, and Evaluation of Diaminopimelic Acid Derivatives as Potential dapF Inhibitors Preventing Lysine Biosynthesis for Antibacterial Activity

open access: yesAntibiotics, 2022
We created thiazole and oxazole analogues of diaminopimelic acid (DAP) by replacing its carboxyl groups and substituting sulphur for the central carbon atom.
Mohd Sayeed Shaikh   +15 more
doaj   +1 more source

Asymmetric Construction of All-Carbon Quaternary Stereocenters by Chiral-Auxiliary-Mediated Claisen Rearrangement and Total Synthesis of (+)-Bakuchiol

open access: yesMolecules, 2012
An asymmetric Claisen rearrangement using Oppolzer’s camphorsultam was developed. Under thermal conditions, a geraniol-derived substrate underwent the rearrangement with good stereoselectivity. The absolute configuration of the newly formed all-
Kin-ichi Tadano   +4 more
doaj   +1 more source

Pd-catalyzed enantioselective intramolecular Heck reaction to access disubstituted dihydroisoquinolinone with a terminal olefin

open access: yesGreen Synthesis and Catalysis, 2021
A first palladium-catalyzed asymmetric intramolecular Heck reaction for the construction 3,4-dihydro-1-(2H)-isoquinolinone containing the quaternary carbon chiral center has been developed.
Sanliang Li   +3 more
doaj   +1 more source

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