✦ LIBER ✦

The synthesis of (6R)-[6-2H]- and (6S)-[6-2H]5-enolpyruvylshikimate-3-phosphate

✍ Scribed by Shankar Balasubramanian; Chris Abell

Book ID: 111714396
Publisher: Elsevier Science
Year: 1991
Tongue: French
Weight: 286 KB
Volume: 32
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)92131-2

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The enantiospecific synthesis of [5-2H]-

The enantiospecific synthesis of [5-2H]-epi-shikimic acid and of (6R) [6-2H]-, (6S) [6-2H]- and [6-2H2] shikimic acid

✍ Lolita O. Zamir; Cong-Danh Nguyen; Shu Wen Li; Anastasia Nikolakakis; Françoise 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 French ⚖ 607 KB

## Abstract The enantioselective synthesis of [5‐^2^H]‐5‐epi‐shikimic acid starting from commercially available L‐shikimic acid has been accomplished in this work. The introduction of the stable isotope was facilitated by an enzymic reduction of a ketone. An interesting stereospecific enolisation w

Inhibition of chorismate synthase by (6R

Inhibition of chorismate synthase by (6R)- and (6S)-6-fluoro-5-enolpyruvylshikimate 3-phosphate

✍ Balasubramanian, Shankar; Davies, Gareth M.; Coggins, John R.; Abell, Chris 📂 Article 📅 1991 🏛 American Chemical Society 🌐 English ⚖ 280 KB

Synthesis of [6″-3H]-, (6″-2H)- and (2-2

Synthesis of [6″-3H]-, (6″-2H)- and (2-2H)-maltotriose

✍ Bernd Sauerbrei; Jutta Niggemann; Stefan Gröger; Sungsook Lee; Heinz G. Floss 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 698 KB

To prepare labeled precursors for biosynthetic studies, methods for the specific introduction of tritium and deuterium into the reducing and the terminal glucose unit of maltotriose were developed. Thus [6"-3H]- and (6"-2H)-maltotriose (17) and (18) were prepared via selective methoxytritylation, de

The synthesis of 6,6,6-2H3-2E-hexenal

✍ Simon Fielder; Daryl D. Rowan 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 French ⚖ 285 KB 👁 1 views

## Abstract 6,6,6‐^2^H~3~‐2E‐Hexenal, leaf‐aldehyde, has been synthesized in 45% yield and 99.3% purity by reaction of 3,3,3‐^2^H~3~‐__n__‐propyl magnesium bromide with an ethereal solution of 3‐trimethylsiloxy‐2‐propenal (3) prepared __in situ__. This new one pot procedure alleviates the need to i

Synthesis of [6-2H] and [6-3H]fecapentae

Synthesis of [6-2H] and [6-3H]fecapentaene-12

✍ Mohamad Z. Kassaee; David G. I. Kingston 📂 Article 📅 1987 🏛 John Wiley and Sons 🌐 French ⚖ 230 KB 👁 1 views

Stereospecific synthesis of (6R)- and (6

Stereospecific synthesis of (6R)- and (6S)-[6-2H1]-D-glucoses

✍ Katsumi Kakinuma 📂 Article 📅 1977 🏛 Elsevier Science 🌐 French ⚖ 233 KB

Although carbohydrate metabolisms have been well studied and importance of carbohydrates as precursors of various natural products is widely understood, little attention has been paid from the stereochemical viewpoints for the fates of a prochiral hydroxymethyl group of &glucose or other carbohydrat