Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Rudolf Beißwenger"'
Autor:
Cäcilia Maichle-Mössmer, Anton Rieker, Rudolf Beißwenger, Medhat El-Mobayed, Gerald Reischl, Klaus Regier
Publikováno v:
Zeitschrift für Naturforschung B. 53:765-773
Bivalent oxidation of 3,5-di-tert-butyl-hydroquinone monoesters leads to phenoxenium ions, which can transfer an acyl group to nucleophiles. Based on this principle, dipeptides, glyco-amino acids and N-sulfonyl-amino acids were synthesized from hydro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8a40d823a05af788e3b0b72d2dca964
https://doi.org/10.1515/znb-1998-0717
https://doi.org/10.1515/znb-1998-0717
Publikováno v:
ChemInform. 22
Sterically hindered phenols are anodically oxidized to the corresponding phenoxenium ions which react with O- and N-nucleophiles to give cyclohexadienyl-protected nucleophiles. 4-Acyloxy substituted phenoxenium ions can transfer the acyl group to nuc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1886a3280190796622e2165e5f838e8
https://doi.org/10.1002/chin.199121268
https://doi.org/10.1002/chin.199121268
Autor:
Anton Rieker, Rudolf Beisswenger, Klaus Regier, G. Reischl, Medhat El-Mobayed, C. Maichle‐Moessmer
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e22cd43947a20c2c61e86e8426bbd0fd
https://doi.org/10.1002/chin.199846223
https://doi.org/10.1002/chin.199846223
Publikováno v:
Tetrahedron. 47:645-654
Sterically hindered phenols are anodically oxidized to the corresponding phenoxenium ions which react with O- and N-nucleophiles to give cyclohexadienyl-protected nucleophiles. 4-Acyloxy substituted phenoxenium ions can transfer the acyl group to nuc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db9b7f6f423474a5034c4f671352e799
https://doi.org/10.1016/s0040-4020(01)87054-x
https://doi.org/10.1016/s0040-4020(01)87054-x
Publikováno v:
Peptide Chemistry 1992 ISBN: 9789401046480
Peptide Chemistry 1992
Peptide Chemistry 1992
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1fcb0293edff3e5520e75ef66679f163
https://doi.org/10.1007/978-94-011-1474-5_19
https://doi.org/10.1007/978-94-011-1474-5_19
Publikováno v:
Liebigs Annalen der Chemie. 1989:337-343
The molecular and crystal structures of the terminally blocked tripeptides methyl α-[(acetyl-α-aminoisobutanoyl-α-aminoisobutanoyl)amino]isobutanoate trihydrate [Ac-(Aib)3-OMe ⋅ 3 H2O, (1)] and methyl α-[(acetyl-α-aminoisobutanoyl-α-aminoisob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::198ac82774b6ecf8cceaaaa0d1443977
https://doi.org/10.1002/jlac.198919890159
https://doi.org/10.1002/jlac.198919890159