✦ LIBER ✦

Peptide synthesis via oxidation of N-acylamino acid phenylhydrazides. III. Dialanylinsulin and (bisphenylalanyl)insulin

✍ Scribed by Milne, H. Bayard; Carpenter, Frederick H.

Book ID: 127141373
Publisher: American Chemical Society
Year: 1968
Tongue: English
Weight: 581 KB
Volume: 33
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo01276a038

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Peptide synthesis via oxidation of N-acy

Peptide synthesis via oxidation of N-acyl-.alpha.-amino acid phenylhydrazides. II. Benzyloxycarbonyl peptide phenylhydrazides

✍ Milne, H. Bayard; Most, Clark F. 📂 Article 📅 1968 🏛 American Chemical Society 🌐 English ⚖ 944 KB

Peptide Synthesis via Oxidation of N-Ace

Peptide Synthesis via Oxidation of N-Acetyl-α-amino Acid Phenylhydrazides 1

✍ Milne, H. Bayard; Kilday, Warren 📂 Article 📅 1965 🏛 American Chemical Society 🌐 English ⚖ 419 KB

N- acylamino acids and peptides III. The

N- acylamino acids and peptides III. The synthesis of N- (feruloyl-2-14C)-glycine-2-3H

✍ H. De Pooter; I. Pé; C. F. Van Sumere 📂 Article 📅 1974 🏛 John Wiley and Sons 🌐 French ⚖ 264 KB

## Abstract N‐(Feruloyl‐2‐^14^C)‐glycine‐2‐^3^H (IX) was obtained with an acceptable yield (43%) starting from O‐methoxycarbonyl‐ferulic acid‐2‐^14^C (IV) and glycine‐2‐^3^H ethyl ester (VI). The latter two compounds were first condensed into N‐(O‐methoxycarbonyl‐feruloyl‐2‐^14^C)‐glycine ‐2‐^3^H e