✦ LIBER ✦

Quantum-chemical modeling of the mechanism for reaction of arenesulfonyl chlorides with α-amino acids

✍ Scribed by L. B. Kochetova; T. P. Kustova; N. V. Kalinina; N. R. Ishkulova; V. V. Lutsyuk

Publisher: Springer
Year: 2011
Tongue: English
Weight: 120 KB
Volume: 47
Category: Article
ISSN: 0040-5760
DOI: 10.1007/s11237-011-9186-x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Chemical and spectroscopical evidence fo

Chemical and spectroscopical evidence for an electron-transfer mechanism in the reaction of arenesulfonyl chlorides with anions

✍ Asensio, Gregorio ;González Núñez, Elena ;Rodrigo, Maria José ;Varea, Teresa 📂 Article 📅 1989 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 273 KB 👁 2 views

Quantum mechanical calculations of amino

Quantum mechanical calculations of amino pyrazole derivatives as corrosion inhibitors for zinc, copper and α-brass in acid chloride solution

✍ A. G. Gad Allah; H. Moustafa 📂 Article 📅 1992 🏛 Springer 🌐 English ⚖ 406 KB

Enantiomer selection in the reaction of

Enantiomer selection in the reaction of N-methyl-α-amino acid N-carboxyanhydride and 3-methyl-5-substituted hydantoin: A model reaction for the stereoselective polymerization of α-amino acid N-carboxyanhydride

✍ Yutaka Hashimoto; Yukio Imanishi 📂 Article 📅 1980 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 677 KB

## Abstract The addition reaction to __N__‐methyl‐(__S__)‐alanine or __N__‐methyl‐(__S__)‐phenylalanine __N__‐car‐boxyanhydride (NCA) of 3‐methyl‐5‐substituted hydantoin (HDT) catalyzed by a tertiary amine was investigated as a model reaction for the propagation reaction of NCA according to the act

Reaction ofN-Acyl-α-triphenylphosphonio-

Reaction ofN-Acyl-α-triphenylphosphonio-α-amino Acid Esters with Organic Bases: Mechanism of the Base-Catalyzed Nucleophilic Substitution of the Triphenylphosphonium Group

✍ Roman Mazurkiewicz; Mirosława Grymel 📂 Article 📅 2002 🏛 Springer Vienna 🌐 English ⚖ 97 KB

Ionic and radical mechanisms in the copp

Ionic and radical mechanisms in the copper-cuprous chloride catalysed reaction of grignards with acid chlorides. Synthesis of α-diketones and hindered di-(sec-alkyl) ketones.

✍ Jacques-Emile Dubois; Michel Boussu 📂 Article 📅 1970 🏛 Elsevier Science 🌐 French ⚖ 181 KB

Investigation of the formation of Streck

Investigation of the formation of Strecker aldehydes from the reaction of Amadori rearrangement products with α-amino acids in low moisture model systems

✍ D. R. Cremer; M. Vollenbroeker; Karl Eichner 📂 Article 📅 2000 🏛 Springer 🌐 English ⚖ 85 KB