✦ LIBER ✦

A highly diastereoselective synthesis of 4-alkyl threo glutamic acids

✍ Scribed by Zi-Qiang Gu; David P. Hesson

Publisher: Elsevier Science
Year: 1995
Tongue: English
Weight: 229 KB
Volume: 6
Category: Article
ISSN: 0957-4166
DOI: 10.1016/0957-4166(95)00274-s

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A highly diastereoselective synthesis of

A highly diastereoselective synthesis of trans-3,4-(difluoromethano)glutamic acid

✍ Akira Shibuya; Masahito Kurishita; Chizuru Ago; Takeo Taguchi 📂 Article 📅 1996 🏛 Elsevier Science 🌐 French ⚖ 515 KB

Diastereoselective Synthesis of Highly S

Diastereoselective Synthesis of Highly Substituted Tetrahydropyran-4-ones.

✍ Paul A. Clarke; William H. C. Martin 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 180 KB 👁 2 views

A New Diastereoselective Synthesis of an

A New Diastereoselective Synthesis of anti-α-Alkyl α-Hydroxy β-Amino Acids

✍ Giuliana Cardillo; Alessandra Tolomelli; Claudia Tomasini 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 215 KB 👁 1 views

Alkylation / Oxazolines / anti-α-Alkyl α-hydroxy β-amino acids / Lithium dianion / Penicillin G acylase As part of an ongoing project concerning the synthesis of conditions, affording in quantitative yield the corresponding hydroxy amides. The starting (R)-3-amino-3-phenyl-enantiomerically pure α-hy

ChemInform Abstract: Stereoselective Syn

ChemInform Abstract: Stereoselective Synthesis of Protected threo-β-Hydroxy-L-glutamic Acid Using a Chiral Aziridine.

✍ Chan Sun Park; Hawn Geun Choi; Hyunjoo Lee; Won Koo Lee; Hyun-Joon Ha 📂 Article 📅 2001 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

A new access to alkyl-α-ketoglutaric aci

A new access to alkyl-α-ketoglutaric acids, precursors of glutamic acid analogues by enzymatic transamination. Application to the synthesis of (2S,4R)-4-propyl-glutamic acid

✍ Virgil Helaine; Joël Rossi; Jean Bolte 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 256 KB

4-Alkyl-2-alkylidene-glutaric acids are easily obtained by a Claisen-Johnson rearrangement, providing a short access to 4-alkyl-ot-ketoglutaric acids. These compounds are substrates of the glutamic oxalacetic transaminase (GOT), allowing the enzymatic synthesis of biologically important analogues of

General Synthesis of optically active 4-

General Synthesis of optically active 4-alkyl (or alkenyl)-γ-lactones from glutamic acid enantiomers

✍ Uzi Ravid; Robert M. Silverstein 📂 Article 📅 1977 🏛 Elsevier Science 🌐 French ⚖ 193 KB