✦ LIBER ✦

Using the same organocatalyst for asymmetric synthesis of both enantiomers of glutamic acid-derived Ni(II) complexes via 1,4-additions of achiral glycine and dehydroalanine Schiff base Ni(II) complexes

✍ Scribed by Belokon, Yuri N.; Gugkaeva, Zalina T.; Hakobyan, Karine V.; Maleev, Victor I.; Moskalenko, Margarita A.; Khrustalev, Victor N.; Saghyan, Ashot S.; Tsaloev, Alan T.; Babievsky, Kiryl K.

Book ID: 113052043
Publisher: Springer
Year: 2011
Tongue: English
Weight: 470 KB
Volume: 43
Category: Article
ISSN: 0939-4451
DOI: 10.1007/s00726-011-1076-y

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Asymmetric Synthesis of L-[β-11C]-3,4-Di

Asymmetric Synthesis of L-[β-11C]-3,4-Dihydroxyphenylalanine via the Chiral Ni(II) Complex of the Schiff Base Derived from (S)-o-N-(N'-Benzylprolyl)aminobenzophenone and Glycine (Ni-BPB-Gly)

✍ O. F. Kuznetsova; I. K. Mosevich; M. V. Korsakov; O. S. Fedorova; R. N. Krasikov 📂 Article 📅 2002 🏛 Springer 🌐 English ⚖ 67 KB

Asymmetric synthesis of α-amino acids vi

Asymmetric synthesis of α-amino acids via homologation of Ni(II) complexes of glycine Schiff bases. Part 2: Aldol, Mannich addition reactions, deracemization and (S) to (R) interconversion of α-amino acids

✍ Sorochinsky, Alexander E.; AceÃ±a, JosÃ© Luis; Moriwaki, Hiroki; Sato, Tatsunori 📂 Article 📅 2013 🏛 Springer 🌐 English ⚖ 995 KB

Why is monoalkylation versus bis-alkylat

Why is monoalkylation versus bis-alkylation of the Ni(II) complex of the Schiff base of (S)-N-(2-benzoylphenyl)-1-benzylpyrrolidine-2-carboxamide and glycine so selective? MP2 modelling and topological QTAIM analysis of chiral metallocomplex synthons of α-amino acids used for the preparation of radiopharmaceuticals for positron emission tomography

✍ Alexander Popkov; Martin Breza 📂 Article 📅 2010 🏛 Springer 🌐 English ⚖ 324 KB