Letters in Peptide Science
1573-496X
0929-5666
Cơ quản chủ quản: N/A
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Các bài báo tiêu biểu
Design of a synthetic adhesion protein by grafting RGD tailed cyclic peptides on bovine serum albumin
Tập 5 Số 2-3 - Trang 87-91 - 1998
Simple and efficient synthesis of chiral amino alcohols with an amino acid-based skeleton
Tập 10 - Trang 79-82 - 2003
Sodium bis(2-methoxyethoxy)aluminum hydride, NaAlH2(OCH2CH2OCH3)2, commercially
known as Vitride® or Red-Al®, enables rapid synthesis of pure optically active
N-protected amino alcohols and peptide alcohols in very high yields. The method
is very simple and attractive, as it does not require an additional step of
N-protected amino acid derivatization and proceeds without the loss of
enantiomeric h...
Synthesis of peptides employing Fmoc-/Boc-/Z-amino acid fluorides and activated commercial zinc dust
Tập 7 - Trang 41-46 - 2000
The coupling of urethane protected amino acidfluorides is accomplished in the
presence ofactivated, commercial zinc dust to synthesize severaldi- and
tripeptides.The coupling was fast and racemization free. The yieldas well as
purity of the peptides was satisfactory.The method was extended for the
incorporation ofsterically hindered α,α-dialkylaminoacids and N-methylamino
acids as well.
Synthesis and matrix assisted laser desorption/ionization time of flight (MALDI-TOF) mass spectrometry study of phosphopeptide
Tập 10 Số 1 - Trang 57-62 - 2003
Facile removal of the N-indole-mesitylenesulfonyl protecting group using HF cleavage conditions
Tập 1 - Trang 163-170 - 1995
Nitrogen indole protection of the β-methyltryptophan side-chain residue is
important for avoiding undesired side reactions during peptide synthesis. Of
great importance is the choice of a side-chain protecting group for orthogonal
peptide synthesis and its stability under a variety of chemical conditions
required for synthesis of the four isomers of this unusual amino acid. We report
here the succ...