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Journal Abstract Search
281 related items for PubMed ID: 7346386
1. Synthesis of 2-(trimethylsilyl)ethyloxycarbonylamino acids and their use in peptide chemistry. Wünsch B, Moroder L, Keller O. Hoppe Seylers Z Physiol Chem; 1981 Sep; 362(9):1289-92. PubMed ID: 7346386 [Abstract] [Full Text] [Related]
2. Caged phospho-amino acid building blocks for solid-phase peptide synthesis. Rothman DM, Vazquez ME, Vogel EM, Imperiali B. J Org Chem; 2003 Aug 22; 68(17):6795-8. PubMed ID: 12919051 [Abstract] [Full Text] [Related]
3. Are PhAcOZ and Nsc suitable N alpha-protecting groups for protease-catalysed peptide synthesis? Braun K, Kuhl P. Pharmazie; 2002 May 22; 57(5):310-2. PubMed ID: 12061253 [Abstract] [Full Text] [Related]
15. Synthesis of nucleopeptides by employing an enzyme-labile urethane protecting group. Jeyaraj DA, Prinz H, Waldman H. Chemistry; 2002 Apr 15; 8(8):1879-87. PubMed ID: 12007098 [Abstract] [Full Text] [Related]
16. Synthesis and properties of oligonucleotides having a chemically stable 2-(trimethylsilyl)benzoyl group. Yamada K, Taguchi H, Ohkubo A, Seio K, Sekine M. Nucleic Acids Symp Ser (Oxf); 2008 Apr 15; (52):301-2. PubMed ID: 18776373 [Abstract] [Full Text] [Related]
17. Convenient synthesis of N-methylamino acids compatible with Fmoc solid-phase peptide synthesis. Biron E, Kessler H. J Org Chem; 2005 Jun 24; 70(13):5183-9. PubMed ID: 15960522 [Abstract] [Full Text] [Related]
18. [Side reactions in peptide synthesis. V. O-sulfonation of serine and threonine during removal of pmc- and mtr-protecting groups from arginine residues in fmoc-solid phase synthesis]. Jaeger E, Remmer HA, Jung G, Metzger J, Oberthür W, Rücknagel KP, Schäfer W, Sonnenbichler J, Zetl I. Biol Chem Hoppe Seyler; 1993 May 24; 374(5):349-62. PubMed ID: 8338636 [Abstract] [Full Text] [Related]