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   <subfield code="a">Comparison of the stepwise and convergent approaches in the solid-phase synthesis of rat Tyro-atriopeptin II</subfield>
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   <subfield code="c">[Dimitrios Gatos, Stella Patrianakou, Olga Hatzi, Kleomenis Barlos]</subfield>
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   <subfield code="a">Summary: Tyro-Atriopeptin II was synthesized on a 2-chlorotrityl resin by both, the stepwise and the convergent approach. For both methods an Fmoc/tBu(Trt)-based protection scheme was used. The convergent methodology utilizes the sequential condensation of four protected peptide fragments. These were chosen so that after every condensation reaction, the amino-terminal region of the newly formed resin-bound peptide did not contain a β-turn. This ‘designed' convergent synthesis gave the target peptide in much higher yield and purity than the conventional stepby-step synthesis.</subfield>
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   <subfield code="t">Letters in Peptide Science</subfield>
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