Results 11 to 20 of about 12,937,378 (338)

Total Synthesis of Sordaricin [PDF]

open access: yesThe Journal of Organic Chemistry, 2003
An enantioconvergent total synthesis of sordaricin (3), the diterpene aglycon of an important class of antifungal compounds, is described. Two approaches were explored, the first of which utilized a possible biogenetic intramolecular [4 + 2] cycloaddition to form the complete carbon skeleton of the target molecule as a single regioisomer 30.
Mander, Lewis, Thomson, Regan
openaire   +9 more sources

Novel Strategies in C-H Oxidations for Natural Product Diversification—A Remote Functionalization Application Summary

open access: yesFrontiers in Chemistry, 2021
Selectively activating the distal inactive C-H bond for functionalization is one of the on-going challenge in organic synthetic chemistry. In recent years, benefiting from the development of selective synthesis methods, novel methodologies not only make ...
Huang Junrong   +11 more
doaj   +1 more source

Total Synthesis of Aeruginazole A [PDF]

open access: yesOrganic Letters, 2011
The first total synthesis of Aeruginazole A, prepared via a convergent strategy that involved both solid-phase peptide synthesis and solution phase chemistry and that enabled conservation of the stereochemistry of the intermediates, is reported.
Bruno, Paolo   +4 more
openaire   +5 more sources

Total Synthesis of (+)-Isatisine A [PDF]

open access: yesThe Journal of Organic Chemistry, 2010
The asymmetric total synthesis of (+)-isatisine A has been accomplished commencing with a Lewis acid-catalyzed cyclization of homochiral (S)-vinylcyclopropane diester and N-tosylindole-2-carboxaldehyde to construct the tetrahydrofuran ring. A palladium-catalyzed oxidative decarboxylation was utilized to obtain the dihydrofuran required for the ...
Avedis Karadeolian, Michael A. Kerr
openaire   +5 more sources

Total Synthesis of (+)‐Cornexistin [PDF]

open access: yesAngewandte Chemie, 2020
AbstractHerein, we describe the first total synthesis of (+)‐cornexistin as well as its 8‐epi‐isomer starting from malic acid. The robust and scalable route features a Nozaki–Hiyama–Kishi reaction, an auxiliary‐controlled syn‐Evans‐aldol reaction, and a highly efficient intramolecular alkylation to form the nine‐membered carbocycle. The delicate maleic
Christian Steinborn   +3 more
openaire   +4 more sources

Total Synthesis of Polysaccharides by Automated Glycan Assembly

open access: yesJournal of the American Chemical Society, 2020
Polysaccharides are the most abundant biopolymers on earth that serve various structural and modulatory functions. Pure, completely defined linear and branched polysaccharides are essential to understand carbohydrate structure and function ...
Abragam A. S. Joseph   +2 more
semanticscholar   +1 more source

Synthesis of the Enantiomers of Thioridazine

open access: yesSynOpen, 2020
Thioridazine, a well-known antipsychotic drug, has shown promising effects on several bacterial strains (including Mycobacterium tuberculosis and methicillin-resistant Staphylococcus aureus).
Simen Antonsen   +7 more
doaj   +1 more source

Total Synthesis of (−)-Isoavenaciolide [PDF]

open access: yesThe Journal of Organic Chemistry, 2013
An enantioselective approach to (-)-isoavenaciolide was achieved starting from 1-undecyn-3-ol. The synthesis relied upon the preparation of a chiral 4-silyloxy-2-alkenylborane by hydroboration of a protected 2,3-allenol and subsequent stereoselective addition to 2-thiophenecarboxaldehyde.
Santos, David   +5 more
openaire   +3 more sources

Total Syntheses of Mycolactone A/B and its Analogues for the Exploration of the Biology of Buruli Ulcer

open access: yesCHIMIA, 2017
Buruli ulcer, classified as a neglected tropical disease by the World Health Organization, is caused by a mycobacterium which secretes a macrolidic exotoxin called mycolactone A/B.
Sarah Saint-Auret   +6 more
doaj   +1 more source

Enantioselective Total Synthesis of (+)-Cassiol [PDF]

open access: yes, 2009
An enantioselective total synthesis of (+)-cassiol is reported. The complex derived from Pd-2(pmdba)(3) and enantiopure t-BuPHOX ligand catalyzes enantioconvergent decarboxylative alkylation to generate the quaternary carbon stereocenter at an early ...
Mohr, Justin T.   +2 more
core   +2 more sources

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