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Barany George
Barany G.
Barany Michael J.
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Michael J.
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http://hub.abes.fr/acs/periodical/joceah/1988/volume_53/issue_22/101021jo00257a009/authorship/2
http://hub.abes.fr/acs/periodical/joceah/2004/volume_69/issue_14/101021jo049830b/authorship/2
http://hub.abes.fr/acs/periodical/joceah/2004/volume_69/issue_12/101021jo049839d/authorship/2
http://hub.abes.fr/acs/periodical/bichaw/2000/volume_39/issue_27/101021bi992927l/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/2005/volume_127/issue_2/101021ja0455446/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/2005/volume_127/issue_2/101021ja0455446/authorship/4
http://hub.abes.fr/acs/periodical/joceah/1990/volume_55/issue_12/101021jo00299a011/authorship/7
http://hub.abes.fr/acs/periodical/jacsat/1985/volume_107/issue_17/101021ja00303a019/authorship/1
http://hub.abes.fr/acs/periodical/bichaw/1993/volume_32/issue_16/101021bi00067a027/authorship/4
http://hub.abes.fr/acs/periodical/joceah/1992/volume_57/issue_11/101021jo00037a013/authorship/4
http://hub.abes.fr/acs/periodical/ancham/1978/volume_50/issue_1/101021ac50023a035/authorship/3
http://hub.abes.fr/springer/periodical/10989/1996/volume_2/issue_5/B943381935BB5DE1E053120B220A297A/authorship/3
http://hub.abes.fr/acs/periodical/joceah/1993/volume_58/issue_18/101021jo00070a041/authorship/5
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Reductive amination with tritylamine as an ammonia equivalent: efficient preparation of the 5-(4-(9-fluorenylmethyloxycarbonyl)aminomethyl-3,5-dimethoxyphenoxy)valeric acid (PAL) handle for peptide synthesis
A new fluoridolyzable anchoring linkage for orthogonal solid-phase peptide synthesis: design, preparation, and application of the N-(3 or 4)-[[4-(hydroxymethyl)phenoxy]-tert-butylphenylsilyl]phenyl pentanedioic acid monoamide (Pbs) handle
Preparation and application of the 5-(4-(9-fluorenylmethyloxycarbonyl)aminomethyl-3,5-dimethoxyphenoxy)-valeric acid (PAL) handle for the solid-phase synthesis of C-terminal peptide amides under mild conditions
S-2,4,6-trimethoxybenzyl (Tmob): a novel cysteine protecting group for the N.alpha.-(9-fluorenylmethoxycarbonyl) (Fmoc) strategy of peptide synthesis
Test for racemization in model peptide synthesis by direct chromatographic separation of diastereomers of the tetrapeptide leucylalanylglycylvaline
Three-dimensional orthogonal protection scheme for solid-phase peptide synthesis under mild conditions
4-(9-Fluorenylmethyloxycarbonyl)phenylhydrazine (FmPH): ANew Chromophoric Reagent for Quantitative Monitoring ofSolid-Phase Aldehydes1-3
Synthesis and Characterization of a β-Hairpin Peptide That Represents a ‘CoreModule' of Bovine Pancreatic Trypsin Inhibitor (BPTI),
On-Resin Native Chemical Ligation for Cyclic Peptide Synthesis1,2
Acid-labile handles for Fmoc solid-phase synthesis of peptide N-alkylamides
Efficient Synthesis of 1,2,4-Dithiazolidine-3,5-diones [Dithiasuccinoyl-Amines]from Bis(chlorocarbonyl)disulfane Plus Bis(trimethylsilyl)amines
Synthesis of phosphotyrosine-containing peptides and their use as substrates for protein tyrosine phosphatases
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