## Abstract Starting from simple aromatic aldehydes and acetylfuran, (__E__)‐1‐(furan‐2‐yl)‐3‐arylprop‐2‐en‐1‐ones (**2**) were synthesized in high yields. Cyclopropanation of the CC bond with trimethylsulfoxonium iodide (Me~3~SO^+^I^−^) furnished (furan‐2‐yl)(2‐arylcyclopropyl)methanones **3** in
Enantioselective synthesis of 2-(3′-alkyl-2′-carboxy cyclopropyl)glycines
✍ Scribed by Angel Mazón; Concepción Pedregal; William Prowse
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 476 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
✦ Synopsis
New conformationally restricted glutamate analogues 2-(3'-alkyl-2'-carboxycyclopropyl)glycines (la-e and 2a-e) were enantioselectively prepared by the addition-elimination reaction of the chiral lithium bislactim ether anion of 3 to racemic 4-alkyl-4-bromobut-2-enoates.
📜 SIMILAR VOLUMES
A route to 1,2,3-trisubstituted cyclopropanes has been developed. The relative stereochemistry at the three cyclopropane centers is established by nucleophilic attack on the pentadienyl ligand on the face opposite to iron and subsequent oxidatively induced reductive elimination with retention of con
A novel enantioselective synthesis of (2S,2%R,3%R)-2-(2%,3%-dicarboxycyclopropyl)glycine (DCG-IV), a potent group II mGluRs agonist is described.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.