𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of (−)-3(R)-amino-4(R),5(R)-dihydroxy-1-cyclohexene-1-carboxylic acid: The 3(R)-amino analogue of (−)-shikimic acid

✍ Scribed by Roger Brettle; Richard Cross; Martyn Frederickson; Edwin Haslam; Gareth M. Davies

Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
220 KB
Volume
6
Category
Article
ISSN
0960-894X

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of (4R*,5R*)-4-acetylamino-5-d
Synthesis of (4R*,5R*)-4-acetylamino-5-diethylcarbamoylcyclohex-1-ene-1-carboxylic acid and (3R*,4R*)-4-acetylamino-3-diethylcarbamoylcyclohex-1-ene-1-carboxylic acid: new inhibitors of influenza virus sialidases
✍ Sean A Kerrigan; Paul W Smith; Richard J Stoodley 📂 Article 📅 2001 🏛 Elsevier Science 🌐 French ⚖ 81 KB

4R\*,5R\*)-4-Acetylamino-5-diethylcarbamoylcyclohex-1-ene-1-carboxylic acid and (3R\*,4R\*)-4-acetylamino-3-diethylcarbamoylcyclohex-1-ene-1-carboxylic acid have been synthesised using a Diels-Alder tactic; both compounds are selective inhibitors of influenza A sialidase, the latter compound being p

Synthesis of (2S,3R)-3-amino-2-hydroxyde
Synthesis of (2S,3R)-3-amino-2-hydroxydecanoic acid and (3R,4R)-3-amino-4-hydroxyazepane from D-isoascorbic acid
✍ Arounarith Tuch; Michèle Sanière; Yves Le Merrer; Jean-Claude Depezay 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 528 KB

Taking advantage of the high functionality of an enantiopure protected syn-2R-amino-l,3,4-triol derivative, easily available on a multigram scale from Disoascorbic acid, several biologically active compounds have been synthesized such as the (2S,3R)-3-amino-2-hydroxydecanoic acid (AHDA), the N-termi