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- W1964162200 abstract "A mild resin-immobilization strategy employing a readily prepared trityl bromide resin for anchoring building blocks via a phenol group has been developed. With Nα-Fmoc-Tyr-OPfp as a starter building block, it was possible to prepare asymmetrically substituted hybrids of spider- and wasp-type polyamine toxins using solid-phase peptide synthesis conditions." @default.
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- W1964162200 date "2005-04-01" @default.
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- W1964162200 title "Side-Chain-Anchored <i>N</i><sup>α</sup>-Fmoc-Tyr-OPfp for Bidirectional Solid-Phase Synthesis" @default.
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- W1964162200 doi "https://doi.org/10.1021/ol050305o" @default.
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