✦ LIBER ✦

Use of the excluded protecting group (EPG) method for peptide synthesis

✍ Scribed by Head, D.B. ;Dong, J.Z. ;Burton, J.A.

Book ID: 110893863
Publisher: John Wiley and Sons
Year: 2005
Tongue: English
Weight: 175 KB
Volume: 65
Category: Article
ISSN: 1397-002X
DOI: 10.1111/j.1399-3011.2005.00243.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Use of the vinyloxycarbonyl group for am

Use of the vinyloxycarbonyl group for amino protection in peptide synthesis

✍ R.A. Olofson; Y.Stephen Yamamoto; David J. Wancowicz 📂 Article 📅 1977 🏛 Elsevier Science 🌐 French ⚖ 252 KB

In this communication we introduce a promising masking agent --the vinyloxycarbonyl or VOC group --for the protection of amino functions in peptide chemistry. Amino acids are easily converted to their N-VOC derivatives (l\_) in dilute aqueous base using the known vinyl chloroformate' in dioxane as t

Acetol: a useful new protecting group fo

Acetol: a useful new protecting group for peptide synthesis

✍ Bijoy Kundu 📂 Article 📅 1992 🏛 Elsevier Science 🌐 French ⚖ 152 KB

Acetol can be conveniently used as a reagent for the protection of carboxylic acids in peptide synthesis. It has been found to be inert and stable to hydrogenolytic and acidolytic conditions normally used in peptide synthesis. Deblocking has been selectively achieved under mild conditions using Bu4N

Protecting Groups for the Enzymatic Pept

Protecting Groups for the Enzymatic Peptide Synthesis

✍ A. FLÖRSHEIMER; A. SCHWARZ; D. STEINKE; M. KITTELMANN; G. HERRMANN; M. R. KULA; 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 178 KB

An Amino-Protecting Group for Use in Pep

An Amino-Protecting Group for Use in Peptide Synthesis Which Can Be Introduced Electrochemically

✍ Dr. Mohamed Hassen Khalifa; Prof. Dr. Günther Jung; Prof. Dr. Anton Rieker 📂 Article 📅 1980 🏛 John Wiley and Sons 🌐 English ⚖ 263 KB

The t-butoxy group, a novel hydroxyl-pro

The t-butoxy group, a novel hydroxyl-protecting group for use in peptide synthesis with hydroxy-amino acids

✍ H. C. Beyerman; J. S. Bontekoe 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 378 KB

## Abstract We have found a novel way of protecting the hydroxyl function in hydroxy‐L‐amino acids, making use of the t‐butoxy group, which is readily split by acids, but not by bases. This group is introduced by acid‐catalysed addition of isobutene to N‐acylated hydroxy‐L‐amino acids. The blockin

Use of polar picolyl protecting groups i

Use of polar picolyl protecting groups in peptide synthesis

✍ Rizo, Josep; Albericio, Fernando; Romero, Guillermo; Garcia-Echeverria, Carlos; 📂 Article 📅 1988 🏛 American Chemical Society 🌐 English ⚖ 592 KB