Results 101 to 110 of about 62,639 (299)

Mapping the Reactivity of the C═C Bond of Cyclic Enol Ether Derivatives of Sugars: Nucleophilicity Parameters of Glycals

open access: yesAngewandte Chemie International Edition, EarlyView.
Endo or Exo? The first quantitative kinetic mapping of the nucleophilic reactivity of endo‐ and exo‐glycal compounds highlighted that endo‐glycals are typically 102 times less reactive than their corresponding parent cyclic enol ethers while exo‐glycals are 103 more nucleophilic. This experimental and computational structure–reactivity study highlights
Sophie Rodrigues   +7 more
wiley   +1 more source

Aziridine-Metathesis based Approaches to Alkaloid Synthesis [PDF]

open access: yes, 2009
The aim of the project is to synthesise (-)-morphine utilising aziridine and metathesischemistry. The thesis is divided into three chapters.Chapter 1 provides brief reviews on the subjects of total synthesis of morphine; ringrearrangementmetathesis (RRM)
Lu, Pengfei, Lu, Pengfei
core  

A regioselectivity switch in Pd-catalyzed hydroallylation of alkynes. [PDF]

open access: yes, 2019
By exploiting the reactivity of a vinyl-Pd species, we control the regioselectivity in hydroallylation of alkynes under Pd-hydride catalysis. A monophosphine ligand and carboxylic acid combination promotes 1,5-dienes through a pathway involving ...
Chen, Qing-An   +5 more
core  

SYNTHESIS, STRUCTURE AND BIOLOGICAL ACTIVITY OF N(4)-ALLYL-3-THIOSEMICARBAZONES AND THEIR COORDINATION COMPOUNDS WITH SOME 3D METALS

open access: yesStudia Universitatis Moldaviae: Stiinte reale si ale naturii, 2016
The paper presents a review of different N(4)-allyl-3-thiosemicarbazones and their coordination compounds described in literature. N(4)-allyl-3-thiosemicarbazide can form corresponding thiosemicarbazones with aliphatic, aromatic and heteroaromatic ...
Vasilii GRAUR
doaj  

Antibacterial properties of surface-active synthesized 1-allyl-3-methylimidazolium based ionic liquids: experimental, molecular docking and DFT calculations

open access: yesResults in Chemistry
Ionic liquids are continuously being synthesized and metathesized with their properties being evaluated, particularly the degradation of these compounds for possible industrial applications.
Vuyolwethu Tokoyi   +6 more
doaj   +1 more source

A Dithio Vinylthio C2 Synthon Enabling Crystalline and Luminescent Sulfur‐Decorated Polymers

open access: yesAngewandte Chemie International Edition, EarlyView.
Transforming CaC2 into a modular C2 building block enables the synthesis of α,ω‐bis(vinylthio) monomer and its conversion into crystalline, sequence‐defined sulfur‐decorated polymers. Their dense thioether clustering induces nonconventional luminescence and provides structure–function control in a more‐sustainable polymer platform.
Bercis Pektas   +4 more
wiley   +1 more source

Auxin-sensitive Aux/IAA proteins mediate drought tolerance in Arabidopsis by regulating glucosinolate levels. [PDF]

open access: yes, 2019
A detailed understanding of abiotic stress tolerance in plants is essential to provide food security in the face of increasingly harsh climatic conditions. Glucosinolates (GLSs) are secondary metabolites found in the Brassicaceae that protect plants from
Ecker, Joseph R   +7 more
core  

A New Monoterpene Isolated from Essential Oil

open access: yesNatural Product Communications, 2017
A new monoterpene 2-allyl-1,4-dihydroxy-5-methylbenzene 1 has been isolated from the essential oil of Nigella sativa seeds along with five known compounds including thymoquinone, carvacrol, dihydrothymoquinone, terpinen-4-ol and dithymoquinone.
Ahmed Benharref   +5 more
doaj   +1 more source

Genetic code expansion for chemosensing and chemical actuation of biological functions

open access: yesBulletin of the Korean Chemical Society, EarlyView.
Genetic code expansion (GCE) broadens the chemical repertoire for precise control of protein function in biological systems. This review highlights GCE‐based sensing and actuating systems that operate through selective interactions between noncanonical amino acids and chemical triggers.
Jieun Bae, Dong‐Hyun Kim, Minseob Koh
wiley   +1 more source

Shedding Light on Synthetic Autocatalysis: From Conventional Closed‐Shell Chemistries to Overlooked Open‐Shell Occurrences

open access: yesChemistry – A European Journal, EarlyView.
Why add another catalyst when the product itself holds the power to catalyze its own formation? Autocatalysis in synthetic chemistry enhances reaction efficiency and uncovers novel catalytic behavior across both closed‐shell and open‐shell systems, expanding reactivity and enabling innovative design strategies.
Jaspreet Kaur, Joshua P. Barham
wiley   +1 more source

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