Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Josiane Thierry"'
Publikováno v:
Orbital: The Electronic Journal of Chemistry, Vol 4, Iss 1, Pp 3-4 (2012)
α-Alloenduracididine, 3-(2-amino-4,5-dihydro-1Himidazole-4-yl)-2-aminopropionic acid)1 and its diastereoisomer, enduracididine 2, are two nonproteinogenic amino acids isolated in 1968 from Streptomyces fungicidicus as part of a cyclopeptide the endu
Externí odkaz:
https://doaj.org/article/cd8ff76abf2b4ca882a985adb4e76fa5
Autor:
Robert H. Dodd, Edmilson José Maria, Diego Rangel Cardoso Silva, Rosa M. Suárez Ordóñez, Kevin Cariou, Josiane Thierry
Publikováno v:
SYNLETT
SYNLETT, Georg Thieme Verlag, 2017, 28 (07), pp.815-818. ⟨10.1055/s-0036-1589935⟩
SYNLETT, Georg Thieme Verlag, 2017, 28 (07), pp.815-818. ⟨10.1055/s-0036-1589935⟩
International audience; A straightforward and efficient preparation of 5-membered cyclic guanidines bearing an ester, a hydroxymethyl or a Weinreb amide functional group at C-4 is described from L-serine. The novel synthetic route provides cyclic gua
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfa55823365272848d54d2ec3dca7535
https://hal.archives-ouvertes.fr/hal-02307213/file/RevisedSynlett2017_KC.pdf
https://hal.archives-ouvertes.fr/hal-02307213/file/RevisedSynlett2017_KC.pdf
Publikováno v:
ChemInform. 45
A one-step, 3-component vinylogous Mannich reaction of trimethylsilyloxyfuran or N-protected tert-butyldimethylsilyloxypyrrole with a variety of nitrogen-containing heterocycles in the presence of diverse electrophiles is described. The reaction prod
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2014, 79 (12), pp.5673-83. ⟨10.1021/jo500827j⟩
Journal of Organic Chemistry, American Chemical Society, 2014, 79 (12), pp.5673-83. ⟨10.1021/jo500827j⟩
International audience; A one-step, 3-component vinylogous Mannich reaction of trimethylsilyloxyfuran or N-protected tert-butyldimethylsilyloxypyrrole with a variety of nitrogen-containing heterocycles in the presence of diverse electrophiles is desc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ba7a3684664cfa6c1b358e0f1881df6
https://hal.archives-ouvertes.fr/hal-01022920
https://hal.archives-ouvertes.fr/hal-01022920
Autor:
Catherine Grillon, Joanna Wdzieczak-Bakala, Pierre Potier, Josiane Thierry, Andrew Riches, Sandrine Gaudron
Publikováno v:
Journal of Peptide Science
Journal of Peptide Science, Wiley, 2001, 7 (5), pp.284-293. ⟨10.1002/psc.322⟩
Journal of Peptide Science, Wiley, 2001, 7 (5), pp.284-293. ⟨10.1002/psc.322⟩
International audience; The tetrapeptide N‐Acetyl‐Ser‐Asp‐Lys‐Pro (AcSDKP), an inhibitor of haematopoietic stem cell proliferation, reduces in vivo and in vitro the damage to the stem cell compartment resulting from treatment with chemother
Autor:
Andrew Riches, Joanna Wdzieczak-Bakala, John Eugenes Chisi, Josiane Thierry, Cecile V. Briscoe
Publikováno v:
STEM CELLS. 17:339-344
Drugs used mainly for the treatment of hypertension, such as angiotensin I-converting enzyme (ACE) inhibitors, can cause pancytopenia. The underlying cause of this side effect remains unknown. In the present study, long-term bone marrow cultures (LTB
Publikováno v:
Tetrahedron Letters. 40:7083-7086
A simple synthesis of various 6-amino-2-substituted hexanoic acids has been developed starting from lysine via the triflate of 6-amino-2-hydroxy hexanoic acid. The same reactions have also been successfully applied starting from the lysyl-proline seq
Publikováno v:
Tetrahedron Letters. 39:1557-1560
2-Phenylisopropyl and t-butyl trichloroacetamidates 1 and 2 are useful reagents for the esterification of N-protected aminoacids under mild neutral conditions. In the case of hydroxyl-containing amino acids, dialkylation occurs but no selectivity cou
Publikováno v:
Tetrahedron Letters. 34:323-326
The esters of Fmoc aminoacids derived from 2-phenylisopropanol have been prepared by using 2-phenylisopropyltrichloroacetimidate 1. They prevent diketopiperazine formation during amino deprotection of dipeptides and can be cleaved in the presence of
Autor:
Braja G. Hazra, Deepak B. Salunke, Vandana S. Pore, Robert H. Dodd, Josiane Thierry, Sudhir N. Bavikar
Publikováno v:
ChemInform. 41
Succinimide esters are subjected to the reaction with azides under conditions A) to give the desired amides within a short time in good yields.