✦ LIBER ✦

A procedure for the facile syntheis of amino-acid N-carboxyanhydrides

✍ Scribed by William D. Fuller; Michael S. Verlander; Murray Goodman

Publisher: Wiley (John Wiley & Sons)
Year: 1976
Tongue: English
Weight: 186 KB
Volume: 15
Category: Article
ISSN: 0006-3525
DOI: 10.1002/bip.1976.360150922

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The initial reaction in strong-base cata

The initial reaction in strong-base catalyzed polymerizations of α-amino acid N-carboxyanhydrides

✍ Murray Goodman; Uriel Arnon 📂 Article 📅 1963 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 209 KB

A Facile, Generally Applicable Synthesis

A Facile, Generally Applicable Synthesis of N-Acetyldehydro-α-amino Acids

✍ Prof. Dr. Franz Effenberger; Thomas Beisswenger 📂 Article 📅 1982 🏛 John Wiley and Sons 🌐 English ⚖ 121 KB 👁 1 views

A New Procedure for the Determination of

A New Procedure for the Determination of the Acidity of Very Strong Acids

✍ F. Klages; K. Bott; P. Hegenberg 📂 Article 📅 1962 🏛 John Wiley and Sons 🌐 English ⚖ 276 KB 👁 2 views

A novel derivatization method with 5-bro

A novel derivatization method with 5-bromonicotinic acid N-hydroxysuccinimide for determination of the amino acid sequences of peptides

✍ Masaru Miyagi; Masayuki Nakao; Takashi Nakazawa; Ikunoshin Kato; Susumu Tsunasaw 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 180 KB 👁 1 views

We have developed a novel method that effectively identifies the N-terminal product ions produced in the tandem mass spectrometry (MS/MS) analysis of peptides done in conjunction with the specific derivatization of the N-terminal amino group using 5-bromonicotinic acid N-hydroxysuccinimide ester (Br

2-(N-Fmoc)-3-(N-Boc-N-methoxy)-diaminopr

2-(N-Fmoc)-3-(N-Boc-N-methoxy)-diaminopropanoic acid, an amino acid for the synthesis of mimics of O-linked glycopeptides

✍ Michael R. Carrasco; Ryan T. Brown; Vu H. Doan; Sean M. Kandel; Franklin C. Lee 📂 Article 📅 2006 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 254 KB

## Abstract Amino acids with __N__‐alkylaminooxy side chains have proven effective for the rapid synthesis of neoglycopeptides. Chemoselective reaction of reducing sugars with peptides containing these amino acids provides glycoconjugates that are structurally similar to their natural counterparts.

The utilization of alanine, glutamic aci

The utilization of alanine, glutamic acid, and serine as amino acid substrates for glycine N-acyltransferase

✍ Francois H. van der Westhuizen; Petrus J. Pretorius; Elardus Erasmus 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 256 KB

The conjugation of benzoyl-CoA with the aliphatic and acidic amino acids by glycine N-acyltransferase, as well as the amides of the latter group, was investigated. Bovine and human liver benzoylamino acid conjugation were investigated using electrospray ionization tandem mass spectrometry (ESI-MS-MS