Synthesis of bis-armed amino acid derivatives via the alkylation of ethyl isocyanoacetate and the Suzuki-Miyaura cross-coupling reaction.

Abstract:

:Two synthetic routes to bis-armed-alpha-amino acid derivatives are described. The first route involves alkylation of dibromo derivatives with ethyl isocyanoacetate under phase-transfer catalysis (PTC) conditions. The second route uses a palladium-mediated Suzuki-Miyaura cross-coupling reaction between a DL-4-boronophenylalanine derivative and aromatic diiodo (or dibromo) compounds.

journal_name

Amino Acids

journal_title

Amino acids

authors

Kotha S,Shah VR,Halder S,Vinodkumar R,Lahiri K

doi

10.1007/s00726-006-0402-2

subject

Has Abstract

pub_date

2007-01-01 00:00:00

pages

387-94

issue

3

eissn

0939-4451

issn

1438-2199

journal_volume

32

pub_type

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