Design of New Photoactivatable Amino Acids: Stereoselective Synthesis of N-Protected Phenylalanine Derivatives as Precursors of p-Diazocyclohexadienone-Containing Peptides

DOI: 10.1021/jo00108a023

Source and publish data:

Journal of Organic Chemistry p. 601 - 607 (1995)

Update date:2022-07-29

Topics:: Authors:

Dugave, C.

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Article abstract of DOI:10.1021/jo00108a023

4-Diazocyclohexa-2,5-dienone-based amino acids m-Dip and o-Dip were designed for building up photoactivatable peptides.Their stable precursors L-3-<3-(benzyloxy)-6-nitrophenyl>alanine (L-m-Nip(Bn)) and L-3-<2-(benzyloxy)-5-nitrophenyl>alanine (L-o-Nip(Bn)

Full text of DOI:10.1021/jo00108a023

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Design of New Photoactivatable Amino Acids: Stereoselective Synthesis of N-Protected Phenylalanine Derivatives as Precursors of p-Diazocyclohexadienone-Containing Peptides

DOI: 10.1021/jo00108a023

Source and publish data:

Authors:

Article abstract of DOI:10.1021/jo00108a023

Full text of DOI:10.1021/jo00108a023

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