Novel Non-PEG Derived Polyethers as Solid Supports. 2. Solid-Phase Synthesis Studies
Author(s) -
Gabriel Cavalli,
Andrew G. Shooter,
David A. Pears,
Donald A. Wellings,
Saeed Gulzar,
Joachim H. G. Steinke
Publication year - 2007
Publication title -
journal of combinatorial chemistry
Language(s) - English
Resource type - Journals
eISSN - 1520-4774
pISSN - 1520-4766
DOI - 10.1021/cc7000887
Subject(s) - solvent , solid phase synthesis , chemistry , peg ratio , reagent , amphiphile , compatibility (geochemistry) , polymer , copolymer , organic chemistry , polymer chemistry , materials science , peptide , biochemistry , finance , economics , composite material
Novel non-PEG derived polyether resins, coined SLURPS (Superior Liquid Uptake Resins for Polymer-supported Synthesis), were studied for their performance in solid-phase synthesis. Novel amino functional resins, SLURPS-NH2, were prepared with a loading of up to 8.5 mmol/g and employed successfully in the solid-phase synthesis of Leu-Enkephalin. The peptide was obtained with the same purity when compared to its synthesis with commercial standard poly(dimethyl acrylamide) resins. Furthermore we show loading and cleavage of aromatic carboxylic acids in excellent yield. The advantageous solvent compatibility of our support was demonstrated through the biphasic dihydroxylation of alkenes with OsO4 in t-BuOH/water mixtures producing bound 1,2-diols and synthesis and removal of a bound oxime using ethanol/water mixtures both in excellent yields. Reactions were easily monitored by gel-phase NMR and FTIR. These results show that SLURPS are very well suited for organic transformations using highly polar solvent mixtures and reagents and at much higher loading levels than standard amphiphilic resins of similar solvent compatibility.
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