Title of article
Synthesis of [18-C-6]-β3-(L)-DOPA, first β-amino acid with a crown-ether receptor side-chain
Author/Authors
Gaucher، نويسنده , , Anne and Barbeau، نويسنده , , Olivier and Hamchaoui، نويسنده , , Wahib and Vandromme، نويسنده , , Lucie and Wright، نويسنده , , Karen and Wakselman، نويسنده , , Michel and Mazaleyrat، نويسنده , , Jean-Paul، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2002
Pages
4
From page
8241
To page
8244
Abstract
Terminally protected Boc-β3-(L)-DOPA-OMe has been synthesized from (L)-DOPA by the Arndt–Eistert homologation procedure. Then, a first crown-ether derivative, Boc-[18-C-6]-β3-(L)-DOPA-OMe, has been obtained by bis-O-alkylation of the catechol function with cyclization, using Cs2CO3 as base and pentaethyleneglycol ditosylate as alkylating agent, in DMF at 60°C.
Keywords
?-Amino acids , ?-Peptides , ?3-(L)-DOPA , Crown-ethers
Journal title
Tetrahedron Letters
Serial Year
2002
Journal title
Tetrahedron Letters
Record number
1658955
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