Results 31 to 40 of about 322,084 (409)

AMIDES ISOLATED FROM THE LEAVES OF Piper tuberculatum Jacq. (Piperaceae) WITH ACETYLCHOLINESTERASE INHIBITION AND LARVICIDAL ACTIVITY AGAINST Aedes aegypti [PDF]

open access: yesQuímica Nova
Piper tuberculatum Jacq. is known to be a promising source of amides, which have shown remarkable biological activities. In this study, a phytochemical investigation of the leaves of P.
Brenda R. C. Leocadio   +10 more
doaj   +1 more source

Homoleptic Bis(trimethylsilyl)amides of Yttrium Complexes Catalyzed Hydroboration Reduction of Amides to Amines.

open access: yesOrganic Letters, 2020
Homoleptic lanthanide complex Y[N(TMS)2]3 is an efficient homogeneous catalyst for the hydroboration reduction of secondary amides and tertiary amides to corresponding amines. A series of amides containing different functional groups such as cyano, nitro,
Pengqing Ye   +7 more
semanticscholar   +1 more source

High-performance light-emitting diodes based on carbene-metal-amides [PDF]

open access: yesScience, 2016
Adding a twist for enhanced performance The efficiency of organic light-emitting diodes (OLEDs) is fundamentally governed by the ratio of emissive singlet to dark triplet excitons that are formed from spin-polarized electron and hole currents within the ...
D. Di   +11 more
semanticscholar   +1 more source

Towards energetically viable asymmetric deprotonations : selectivity at more elevated temperatures with C2-symmetric magnesium bisamides [PDF]

open access: yes, 2011
A novel chiral magnesium bisamide has enabled the development of effective asymmetric deprotonation protocols at substantially more elevated temperatures.
Aggarwal   +54 more
core   +1 more source

Progress on Cassaine-Type Diterpenoid Ester Amines and Amides ( Alkaloids)

open access: yesNatural Product Communications, 2006
The structures, spectral characteristics, and bioactivities of 39 natural cassaine-type diterpenoid ester amines and amides (Erythrophleum alkaloids) and 31 synthetic analogues are reviewed.
Jing Qu   +5 more
doaj   +1 more source

Enhancing the cellular uptake of Py–Im polyamides through next-generation aryl turns [PDF]

open access: yes, 2012
Pyrrole–imidazole (Py–Im) hairpin polyamides are a class of programmable, sequence-specific DNA binding oligomers capable of disrupting protein–DNA interactions and modulating gene expression in living cells.
Baird   +54 more
core   +2 more sources

Nitromethane as a nitrogen donor in Schmidt-type formation of amides and nitriles

open access: yesScience, 2019
Sourcing nitrogen from nitromethane Nitromethane is produced in bulk quantities for use as a solvent. Its applications as a reagent have focused mainly on the acidity of the methyl protons en route to modifying the carbon center. Liu et al. now report an
Jianzhong Liu   +8 more
semanticscholar   +1 more source

Asymmetric synthesis of γ-chloro-α,β-diamino- and β,γ-aziridino-α-aminoacylpyrrolidines and -piperidines via stereoselective Mannich-type additions of N-(diphenylmethylene)glycinamides across α-chloro-N-sulfinylimines [PDF]

open access: yes, 2012
The asymmetric synthesis of new chiral gamma-chloro-alpha,beta-diaminocarboxylamide derivatives by highly diastereoselective Mannich-type reactions of N-(diphenylmethylene) glycinamides across chiral alpha-chloro-N-p-toluenesulfinylaldimines was ...
Augustyns, Koen   +5 more
core   +3 more sources

Safety assessment of the mixture of methyl-branched and linear C14–C18 alkanamides, derived from fatty acids, for use in food contact materials [PDF]

open access: yes, 2017
Publisher ...
Barthélemy, Eric   +24 more
core   +3 more sources

Photoinduced Remote Functionalization of Amides and Amines Using Electrophilic Nitrogen Radicals

open access: yesAngewandte Chemie, 2018
The selective functionalization of C(sp3)−H bonds at distal positions to functional groups is a challenging task in synthetic chemistry. Reported here is a photoinduced radical cascade strategy for the divergent functionalization of amides and protected ...
Sara P. Morcillo   +5 more
semanticscholar   +1 more source

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