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- W2008234297 abstract "Aspartimide prone sequence containing protected peptides are successfully synthesized in solid phase by using the bifunctional linker N-[(9-hydroxymethyl)-2-fluorenyl] succinamic acid (HMFS) in combination with morpholine as the cleavage reagent. Access to high purity peptide synthons opens a straightforward way to the synthesis of large proteins by convergent strategies." @default.
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- W2008234297 date "2000-10-01" @default.
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- W2008234297 title "Synthesis of aspartimide-free protected peptides on base-labile functionalized resins" @default.
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