SYNTHESIS OF N-PROTECTED SERINE ETHERS AS PRECURSORS OF NEW PHOTOACTIVATABLE AMINO-ACIDS CLEAVABLE BY HYDROGENOLYSIS

Authors
DUGAVE C KESSLER P COLAS C HIRTH C
Citation
C. Dugave et al., SYNTHESIS OF N-PROTECTED SERINE ETHERS AS PRECURSORS OF NEW PHOTOACTIVATABLE AMINO-ACIDS CLEAVABLE BY HYDROGENOLYSIS, Tetrahedron letters, 35(49), 1994, pp. 9199-9202
Citations number
13
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
35
Issue
49
Year of publication
1994
Pages
9199 - 9202
Database
ISI
SICI code
0040-4039(1994)35:49<9199:SONSEA>2.0.ZU;2-R
Abstract
Fmoc-(L)-serine ethers bearing either 2-(2'-methoxyethoxymethyl ether) -5-terbutyloxycarbonylaminobenzyl (ortho) or 5-(2'-methoxyethoxymethyl ether)-2-terbutyloxycarbonylaminobenzyl (metal moieties were synthesi zed. Spectral characteristics of the corresponding photoactivatable 4- diazocyclohexa-2,5-dienones were determined.