Results 171 to 180 of about 177,307 (324)

Engineering Polyketide Stereocenters with Ketoreductase Domain Exchanges. [PDF]

open access: yesJ Am Chem Soc
Keiser LS   +12 more
europepmc   +1 more source

Acyclic Nucleoside Phosphonates As Potential Inhibitors Of Plasmodium Falciparum Egress

open access: yesChemistry – A European Journal, EarlyView.
Exploration of the chemistry of acyclic nucleoside phosphonates allowed us to study structural diversity from the hit compound; biological evaluation and molecular docking were performed to decipher key interactions with the putative target. Abstract The emergence of drug‐resistant Plasmodium strains requires the development of novel antimalarial ...
Thomas Cheviet   +6 more
wiley   +1 more source

Author Correction: Tripterygium wilfordii cytochrome P450s catalyze the methyl shift and epoxidations in the biosynthesis of triptonide. [PDF]

open access: yesNat Commun
Kongstad KT   +7 more
europepmc   +1 more source

Synthesis and determination of absolute stereochemistry of Gosodesmine

open access: hybrid
Mir Mohd Ikhlaq   +3 more
openalex   +1 more source

Development of Synthetic Routes to 2′‐O,4′‐C‐Spirocyclopentylene‐Bridged Nucleic Acids: Thymidine, Guanosine, and Adenosine

open access: yesChemistry – A European Journal, EarlyView.
A novel synthetic route to 2′‐O,4′‐C‐spirocyclopentylene‐bridged nucleic acid (scpBNA2) monomers bearing thymine, guanine, and adenine nucleobases. The strategy integrates 2′,4′‐lactonization, transglycosylation, and intramolecular iodocyclization, thereby bypassing the 2′‐OH inversion step and providing scpBNA2 nucleoside building blocks for antisense
Riku Kumagai   +3 more
wiley   +1 more source

Stereochemistry Drives the Macromolecular Conformation and Biological Activity of Glycopolymers. [PDF]

open access: yesACS Cent Sci
Ishaq MW   +5 more
europepmc   +1 more source

Regio‐ and Stereocontrolled‐Synthesis of a Heterocycle Fragment Collection Using Palladium Catalyzed C‐H Arylation

open access: yesChemistry – A European Journal, EarlyView.
44 novel heterocycle fragments are prepared through a C–H functionalization strategy. Systematic variation of exit vectors and polar functionality provides a set of fragments that sit in attractive fragment chemical space. Abstract Saturated heterocycles are valuable fragments in drug discovery due to their polarity, 3D structure, and potential for ...
Amalia‐Sofia Piticari   +5 more
wiley   +1 more source

De Novo Design and Asymmetric Synthesis of a <i>C</i>-1/2 Benzodioxin Fused Glycoside Analogue of Lincomycin. [PDF]

open access: yesOrg Lett
Hicks I   +6 more
europepmc   +1 more source

Enantiospecific, Regioselective Cross-Coupling Reactions of Secondary Allylic Boronic Esters [PDF]

open access: yes, 2013
Aggarwal, Varinder K.   +5 more
core   +1 more source

Home - About - Disclaimer - Privacy