Synthesis of N-protected serine ethers as precursors of new photoactivatable amino acids cleavable by hydrogenolysis

DOI: 10.1016/0040-4039(94)88465-X

Source and publish data:

Tetrahedron Letters p. 9199 - 9202 (1994)

Update date:2022-07-29

Topics:

Authors:

Dugave, Christophe

Kessler, Pascal

Colas, Christophe

Hirth, Christian

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Article abstract of DOI:10.1016/0040-4039(94)88465-X

Fmoc-(L)-serine ethers bearing either 2-(2'-methoxyethoxymerhyl ether)-5-terbutyloxycarbonylaminobenzyl (ortho) or 5-(2'-methoxyethoxymethy] ether)-2-terbutyloxycarbonylaminobenzyl (metal moieties were synthesized. Spectral characteristics of the corresponding photoactivatable 4-diazocyclohexa-2,5-dienones were determined.

Full text of DOI:10.1016/0040-4039(94)88465-X

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