Selective cleavage of the allyl and allyloxycarbonyl groups through palladium-catalyzed hydrostannolysis with tributyltin hydride. Application to the selective protection-deprotection of amino acid derivatives and in peptide synthesis

Selective cleavage of the allyl and allyloxycarbonyl groups through palladium-catalyzed hydrostannolysis with tributyltin hydride. Application to the selective protection-deprotection of amino acid derivatives and in peptide synthesis

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Veröffentlicht in:Journal of organic chemistry 1987-10, Vol.52 (22), p.4984-4993
Hauptverfasser: DANGLES, O, GUIBE, F, BALAVOINE, G, LAVIELLE, S, MARQUET, A
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Sprache:eng
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Chemistry
Exact sciences and technology
Organic chemistry
Peptides
Preparations and properties
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container_end_page 4993
container_issue 22
container_start_page 4984
container_title Journal of organic chemistry
container_volume 52
creator DANGLES, O
GUIBE, F
BALAVOINE, G
LAVIELLE, S
MARQUET, A
description
doi_str_mv 10.1021/jo00231a027
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ispartof Journal of organic chemistry, 1987-10, Vol.52 (22), p.4984-4993
issn 0022-3263
1520-6904
language eng
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source American Chemical Society Journals
subjects Chemistry
Exact sciences and technology
Organic chemistry
Peptides
Preparations and properties
title Selective cleavage of the allyl and allyloxycarbonyl groups through palladium-catalyzed hydrostannolysis with tributyltin hydride. Application to the selective protection-deprotection of amino acid derivatives and in peptide synthesis
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