A Novel Strategy Towards the Asymmetric Synthesis of Orthogonally Funtionalised 2-N-Benzyl-N-α-methylbenzylamino- 5-carboxymethyl-cyclopentane-1-carboxylic acid.

A Novel Strategy Towards the Asymmetric Synthesis of Orthogonally Funtionalised 2-N-Benzyl-N-α-methylbenzylamino- 5-carboxymethyl-cyclopentane-1-carboxylic acid.

The asymmetric synthesis of the orthogonally funtionalised compounds tert-butyl 2-N-benzyl-N-α-methylbenzylamino-5-methoxycarbonylmethylcyclopentane- 1-carboxylate and methyl 2-N-benzyl-N-α-methylbenzylamino-5–carboxymethylcyclo- pentane-1-carboxylate by a domino reaction of tert-butyl me...

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Bibliographic Details
Main Authors: Julio G. Urones, Mercedes García, David Díez, Mohamed M. El Hammoumi, Narciso M. Garrido
Format: Article
Language:English
Published: MDPI AG 2004-04-01
Series:Molecules
Subjects:
Asymmetric synthesis
chiral lithium amide
β-amino acids
domino reaction
β-aminocyclopentane carboxilate
aminodiester orthogonal protection.
Online Access:http://www.mdpi.com/1420-3049/9/5/373/

Internet

http://www.mdpi.com/1420-3049/9/5/373/

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