✦ LIBER ✦

THE ACTION OF SOME α-METHYL AND OTHER AMINO ACIDS ON CEREBRAL CATECHOLAMINES

✍ Scribed by T. L. Sourkes; G. F. Murphy; Beatriz Chavez; Marie Zielinska

Book ID: 111164621
Publisher: John Wiley and Sons
Year: 1961
Tongue: English
Weight: 343 KB
Volume: 8
Category: Article
ISSN: 0022-3042
DOI: 10.1111/j.1471-4159.1961.tb13532.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Action of some Water-soluble Poly-α-Amin

Action of some Water-soluble Poly-α-Amino-Acids on Bacteria

✍ KATCHALSKI, E.; BICHOVSKI-SLOMNITZKI, L.; VOLCANI, B. E. 📂 Article 📅 1952 🏛 Nature Publishing Group 🌐 English ⚖ 231 KB

On the pharmacology of α-methylated cate

On the pharmacology of α-methylated catecholamines and the mechanism of the antihypertensive action of α-methyldopa

✍ Peter Holtz; Dieter Palm 📂 Article 📅 1967 🏛 Elsevier Science 🌐 English ⚖ 375 KB

THE ACTION OF PERIODIC ACID ON α-AMINO A

THE ACTION OF PERIODIC ACID ON α-AMINO ALCOHOLS

✍ Nicolet, Ben H.; Shinn, Leo A. 📂 Article 📅 1939 🏛 American Chemical Society 🌐 English ⚖ 117 KB

Highly Practical Methodology for the Syn

Highly Practical Methodology for the Synthesis of d- and l-α-Amino Acids, N-Protected α-Amino Acids, and N-Methyl-α-amino Acids

✍ Myers, Andrew G.; Gleason, James L.; Yoon, Taeyoung; Kung, Daniel W. 📂 Article 📅 1997 🏛 American Chemical Society 🌐 English ⚖ 602 KB

The action of nitrous acid on some amino

The action of nitrous acid on some amino-methylpyrimidines

✍ D.T. Hurst 📂 Article 📅 1970 🏛 Elsevier Science 🌐 French ⚖ 88 KB

Synthesis of enantiopure (αMe)Dip and ot

Synthesis of enantiopure (αMe)Dip and other α-methylated β-branched amino acid derivatives

✍ Alberto Avenoza; Jesús H. Busto; Carlos Cativiela; Jesús M. Peregrina; David Suc 📂 Article 📅 2003 🏛 Elsevier Science 🌐 English ⚖ 290 KB

This report describes the synthesis of the two enantiomerically pure a-methylated b-branched phenylalanine derivatives, (S)-and (R)-a-methyl-b,b-diphenylalanine-(aMe)Dip-starting from the chiral building blocks (R)-and (S)-N-Boc-N,O-isopropylidene-a-methylserine methyl esters, respectively. The key