The stereoselective synthesis of carbohydrates and related bioactive compounds containing
a polyhydroxylated chain embedded in their structural framework remains a topic of great …

The identification of a series of compounds that specifically inhibit efflux by the MexAB-OprM
pump system in Pseudomonas aeruginosa is described. Synthesis and in vitro structure …

γ-Siloxyallyltributylstannanes were selectively obtained as E or Z isomers from β-
tributylstannylacrolein upon reaction with lithium or magnesium alkylcyanocuprates. The …

A two-step synthesis of C-septanosides from pyranoses is reported. Vinyl addition to tetra-O-
benzyl d-glucose, d-galactose, and d-mannose gave the corresponding allylic alcohols …

Abstract Optically active (3R, 4R)‐3, 4‐diacetoxypyrrolidine‐2, 5‐dione was prepared from l‐
tartaric acid by ring closure of the ammonium salt of (2R, 3R)‐2, 3‐diacetoxy‐3 …

An efficient, divergent, and straightforward access to novel C-glycosides has been
developed, namely, α-hydroxy carboxamide and carboxylic acid derivatives, via a green and …

Decontamination of polluted soils using plants is based on the ability of plant species
(including transgenic plants) to enhance bioavailability of pollutants in the rhizosphere and …

Synthesis of a complex disaccharide precursor of phosphonate analogues of the antibiotic
moenomycin A12 - ScienceDirect Skip to main contentSkip to article Elsevier logo Journals & …

Gawro nski and Gawro nska summarized 150 years of tartaric acid history in their
monograph titled “Tartaric and Malic Acids in Synthesis”. 1 This is a fascinating story of a …

Abstract (DE) SUMMARY The moenomycin-type compounds are known to inhibit selectively
the enzyme penicillin binding protein 1b (PBP 1b) that catalyses the transglycosylation …