Résultats de la recherche

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Selected Methodologies Convenient for the Synthesis of N,5-Diaryloxazole-2-amine Pharmacophore
Enantioselective Access to Key Intermediates for Salvinorin A and Analogues
First Total Synthesis of Pamamycin-621D
Ynamide Click chemistry in development of triazole VEGFR2 TK modulators
Mild deprotection of PMB ethers using tert-butyl bromide
Diastereoselective synthesis of the C14-C29 fragment of amphidinol 3
Isolation, structural determination, and synthetic approaches toward amphidinol 3
Access towards enantiopure α,α-difluoromethyl alcohols by means of sulfoxides as traceless chiral auxiliaries
Access to Wieland–Miescher Diketone-Derived Building Blocks by Stereoselective Construction of the C-9 Quaternary Carbon Center Using the Mukaiyama Aldol Reaction
FeCl3.6H2O/acetaldehyde, a versatile system for the deprotection of ketals and acetals via a transacetalization process
Novel CLK1 inhibitors based on N-aryloxazol-2-amine skeleton - A possible way to dual VEGFR2 TK/CLK ligands
Diastereoselective synthesis of the C17-C30 fragment of amphidinol 3
Quinoides and VEGFR2 TKIs influence the fate of hepatocellular carcinoma and its cancer stem cells
Convergent total synthesis of (±) myricanol, a cyclic natural diarylheptanoid
Synthesis, biological evaluation and molecular modeling studies on novel quinonoid inhibitors of CDC25 phosphatases

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