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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

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✦ 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.


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