Results 61 to 70 of about 4,055,225 (307)

Asymmetric total synthesis of alkaloid natural products without external chiral sources [PDF]

open access: yes, 2018
The chirality of a starting material having a chiral sp3-carbon can be preserved under some circumstances in the reaction product even though the reaction proceeds at the chiral carbon as a reaction center through reactive intermediates.
Kim, Sanghee
core  

Continuous-Flow Synthesis of the Nucleobase Unit of Remdesivir

open access: yesEngineering, 2023
In this work, the nucleobase unit of the antiviral drug remdesivir, 7-bromopyrrolo[2,1-f][1,2,4]triazin-4-amine, was synthesized through five-step continuous flow.
Yongxing Guo   +5 more
doaj  

ChemInform Abstract: Chemical Asymmetric Synthesis

open access: yesChemInform, 1989
Thalidomide comes in two forms: a left-handed compound which is a powerful tranquilizer, and a right-handed version which can disrupt fetal development causing severe handicap. As a necessary consequence of synthetic methods available in the early 1960s the two forms were present in equal proportions in the manufactured drug, with catastrophic ...
Brown, J, Davies, S
openaire   +4 more sources

Heterogenisation of ketone catalysts within mesoporous supports for asymmetric epoxidation

open access: yes, 2013
The synthesis of the first mesoporous silica (150 Å) anchored carbohydrate-derived chiral ketone is described. This new heterogeneous catalyst has been shown to be effective in the asymmetric epoxidation of olefins by oxone.
Adam   +60 more
core   +1 more source

Development of fluorine-substituted NH2-biphenyl-diarylpyrimidines as highly potent non-nucleoside reverse transcriptase inhibitors: Boosting the safety and metabolic stability

open access: yesActa Pharmaceutica Sinica B, 2023
Our recent studies for nonnucleoside reverse transcriptase inhibitors identified a highly potent compound JK-4b against WT HIV-1 (EC50 = 1.0 nmol/L), but the poor metabolic stability in human liver microsomes (t1/2 = 14.6 min) and insufficient ...
Xin Jin   +9 more
doaj  

Asymmetric synthesis of gonytolide A: strategic use of an aryl halide blocking group for oxidative coupling [PDF]

open access: yes, 2018
The first synthesis of the chromanone lactone dimer gonytolide A has been achieved employing vanadium(V)-mediated oxidative coupling of the monomer gonytolide C. An o-bromine blocking group strategy was employed to favor para- para coupling and to enable
Iwata, Takayuki   +5 more
core   +1 more source

Catalytic enantioselective intramolecular hydroamination of alkenes using chiral aprotic cyclic urea ligand on manganese (II)

open access: yesNature Communications
Asymmetric catalysis for enantioselective intramolecular hydroamination of alkenes is a critical method in the construction of enantioenriched nitrogen-containing rings, often prevalent in biologically active compounds and natural products.
Bin Cui   +6 more
doaj   +1 more source

Transition metal-catalyzed branch-selective hydroformylation of olefins in organic synthesis

open access: yesGreen Synthesis and Catalysis, 2021
Hydroformylation of olefins can generate linear and branched aldehydes, and the branched aldehydes are attractive precursors for the synthesis of fine chemicals and pharmaceuticals.
Yingtang Ning   +2 more
doaj  

Catalytic Asymmetric Synthesis of Butenolides and Butyrolactones

open access: yesChemical Reviews, 2017
γ-Butenolides, γ-butyrolactones, and derivatives, especially in enantiomerically pure form, constitute the structural core of numerous natural products which display an impressive range of biological activities which are important for the development of ...
B. Mao   +2 more
semanticscholar   +1 more source

Crystal structure of 2-(8-bromo-2-phenylimidazo[1,2-α]pyridin-3-yl)-6,7-dimethyl-3-phenylquinoxaline, C29H21BrN4

open access: yesZeitschrift für Kristallographie - New Crystal Structures, 2018
C29H21BrN4, orthorhombic, Pca21 (no. 29), a = 15.6577(5) Å, b = 9.6445(3) Å, c = 31.1869(10) Å, V = 4709.6(2) Å3, Z = 8, Rgt(F) = 0.0435, wRref(F2) = 0.0779, T = 293(2) K.
Song Gui Ting, Meng Jiang Ping, Zhu Jin
doaj   +1 more source

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