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
Link To Document :
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