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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
Mild deprotection of PMB ethers using tert-butyl bromide
Isolation, structural determination, and synthetic approaches toward amphidinol 3
Iron-catalyzed cross-coupling between C-bromo mannopyranoside derivatives and a vinyl Grignard reagent: toward the synthesis of the C31-C52 fragment of amphidinol 3
Diastereoselective synthesis of the C14-C29 fragment of amphidinol 3
Access towards enantiopure α,α-difluoromethyl alcohols by means of sulfoxides as traceless chiral auxiliaries
Ynamide Click chemistry in development of triazole VEGFR2 TK modulators
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
Access to Wieland–Miescher Diketone-Derived Building Blocks by Stereoselective Construction of the C-9 Quaternary Carbon Center Using the Mukaiyama Aldol Reaction
Diastereoselective synthesis of the C17-C30 fragment of amphidinol 3
Development of Novel Oxotriazinoindole Inhibitors of Aldose Reductase
Unintended Formation of a 26-Membered Cycle in the Course of a Novel Approach to Myricanol, a Strained [7,0]-Metacyclophane
Synthesis and use of trifluoromethylthiolated ketenimines
Quinoides and VEGFR2 TKIs influence the fate of hepatocellular carcinoma and its cancer stem cells
Design, synthesis and biological evaluation of antimicrobial diarylimine and –amine compounds targeting the interaction between the bacterial NusB and NusE proteins
Efficient asymmetric synthesis of aryl difluoromethyl sulfoxides and their use to access enantiopure α-difluoromethyl alcohols
Convergent total synthesis of (±) myricanol, a cyclic natural diarylheptanoid

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