Results 181 to 190 of about 74,560 (387)
This paper reports on creating a novel synthetic route of kanamycins A and B using the desymmetric boron‐mediated aglycon delivery (BMAD) reaction of meso‐diol acceptor with 1,2‐anhydro donor and regio‐ and stereoselective glycosylation of diol acceptor with trichloroacetimidate donor for introduction of a set of challenging 1,2‐cis‐glycosidic linkages
Kanae Hosomi+7 more
wiley +1 more source
Strategy‐Level Prodrug Synthesis
Prodrug approaches can be expanded by increasing options for controlling site‐selective functionalization, boosting the range of linking groups, and enhancing the chemoselectivity of reactive group incorporation. This Concept describes strategy‐level prodrug synthesis, whereby these issues are addressed at an early stage of a sequence.
Paul J. Geaneotes, Paul E. Floreancig
wiley +1 more source
Studies on Carbamates. XV. The Carbamates of alpha-Aminocaproic Acid, epsilon-Aminocaproic Acid and alpha,epsilon-Diaminocaproic Acid. [PDF]
Mogens Ballund Jensen+4 more
openalex +1 more source
Highly reactive (aza)quinone methides are electrophiles generated from many stimuli‐responsive prodrugs and probes. A new linker has been designed to quench the electrophilic methide, forming a tetrahydroisoquinoline (THIQ) heterocycle in high yields, even when a competing nucleophile is present.
Veera V. Shivaji R. Edupuganti+7 more
wiley +1 more source
Cucumber (Cucumis sativa), a widely consumed vegetable, often faces issues with pests and diseases, leading to the excessive use of pesticides during its cultivation.
Evans Ntim AMEDOR+2 more
doaj
The Initiating Action of Ethyl Carbamate (Urethane) on Mouse Skin
I. Berenblum, Nechama Haran
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The serine capsid protease (CP) catalyzes a crucial process of the alphaviral replication cycle; therefore, it constitutes an interesting therapy target. Herein, the O'nyong‐nyong virus CP profile activity with a specific fluorogenic substrate is analyzed and examines the inhibitory activity of a new series of phosphonic analogs of tryptophan and ...
Karolina Torzyk‐Jurowska+5 more
wiley +1 more source
This article describes the development of improved NEU1 inhibitors based on the 2‐deoxy‐2,3‐didehydro‐N‐acetyl neuraminic acid scaffold. A series of candidate inhibitors are designed containing bioisosteres of the C5‐amide group and evaluated for activity against NEU1‐4 enzymes.
Mostafa Radwan+2 more
wiley +1 more source
Adamantane derivatives are promising candidates in the design of new materials with unique properties. In this study, we investigated the molecular structure of a series of adamantyl esters and ethers with an increasing substituent size using broadband rotational spectroscopy.
Nataša Burić+5 more
wiley +1 more source
Carbamates and related derivatives are crucial skeletons for pesticide design and pharmaceutical chemistry. Recently, a synthetic route for the production of carbamates has drawn great attention, which assembles the economical, renewable and non-toxic ...
Yanyan Gong+4 more
doaj