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http://hub.abes.fr/acs/periodical/joceah/1977/volume_42/issue_23/101021jo00443a040/authorship/4
http://hub.abes.fr/acs/periodical/bichaw/1991/volume_30/issue_43/101021bi00107a020/authorship/8
http://hub.abes.fr/acs/periodical/jacsat/1978/volume_100/issue_5/101021ja00473a038/authorship/5
http://hub.abes.fr/acs/periodical/bichaw/2006/volume_45/issue_11/101021bi052388m/authorship/5
http://hub.abes.fr/acs/periodical/bichaw/2002/volume_41/issue_50/101021bi026590q/authorship/5
http://hub.abes.fr/acs/periodical/bichaw/2003/volume_42/issue_29/101021bi034426c/authorship/6
http://hub.abes.fr/acs/periodical/bichaw/2004/volume_43/issue_51/101021bi048040t/authorship/5
http://hub.abes.fr/acs/periodical/bichaw/2006/volume_45/issue_40/101021bi060662m/authorship/8
http://hub.abes.fr/acs/periodical/joceah/1987/volume_52/issue_22/101021jo00231a027/authorship/5
http://hub.abes.fr/acs/periodical/jmcmar/1984/volume_27/issue_9/101021jm00375a027/authorship/4
http://hub.abes.fr/acs/periodical/joceah/1988/volume_53/issue_14/101021jo00249a006/authorship/4
http://hub.abes.fr/acs/periodical/joceah/1985/volume_50/issue_17/101021jo00217a029/authorship/3
http://hub.abes.fr/acs/periodical/joceah/1989/volume_54/issue_2/101021jo00263a048/authorship/3
http://hub.abes.fr/acs/periodical/joceah/1983/volume_48/issue_10/101021jo00158a033/authorship/3
http://hub.abes.fr/acs/periodical/joceah/1982/volume_47/issue_12/101021jo00133a004/authorship/3
http://hub.abes.fr/acs/periodical/bichaw/1980/volume_19/issue_13/101021bi00554a036/authorship/5
http://hub.abes.fr/acs/periodical/jacsat/1981/volume_103/issue_2/101021ja00392a034/authorship/3
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On the mechanism of the conversion of dethiobiotin to biotin in E. coli. Studies with deuterated precursors using tandem mass spectroscopic (MS-MS) techniques
L-Threo- and L-erythro-3-fluoroglutamic acids. Synthesis by fluorodehydroxylation and enzymic resolution
Facile synthesis of optically pure (2R,3R)- and (2R,3S)-3-fluoroglutamic acids using glutamate dehydrogenase
Vitamin K dependent carboxylation: synthesis and biological properties of tetrazolyl analogs of pentapeptidic substrates
Transformation of methionine into S-tert-butylhomocysteine. Application to a methionine-containing peptide: substance P
A new modified amino acid. 2-Amino-3-mercapto-3-phenylpropionic acid (3-mercaptophenylalanine). Synthesis of derivatives, separation of stereoisomers, and assignment of absolute configuration
A total synthesis of biotin based on the stereoselective alkylation of sulfoxides
Iron−Sulfur Clusters of Biotin Synthase In Vivo: A Mössbauer Study
Fate of the (2Fe-2S)2+ Cluster of Escherichia coli Biotin Synthase during Reaction:A Mössbauer Characterization
Further Investigation on the Turnover of Escherichia coli Biotin Synthase withDethiobiotin and 9-Mercaptodethiobiotin as Substrates
Escherichia coli Biotin Synthase Produces Selenobiotin. Further Evidence of theInvolvement of the [2Fe-2S]2+ Cluster in the Sulfur Insertion Step
Biotin Synthase Mechanism: Mutagenesis of the YNHNLD Conserved Motif,
Mechanism of the antibiotic action of .alpha.-dehydrobiotin
Vitamin K dependent carboxylation: determination of the stereochemical course using a 4-fluoroglutamyl-containing substrate
A reinvestigation of the mechanism of Pseudomonas testosteroni .DELTA.5-3-ketosteroid isomerase
Selective cleavage of the allyl and (allyloxy)carbonyl groups through palladium-catalyzed hydrostannolysis with tributyltin hydride. Application to the selective protection-deprotection of amino acid derivatives and in peptide synthesis
Deuterium or tritium labeling by ionic hydrogenation. A convenient route to specifically labeled dethiobiotin
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