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pro vyhledávání: '"Katja Schultz"'
This study aims to investigate the wave boundary layer and the turbulentairflow above wind waves on slick-free and slick-covered water surfaces. To realizethis, we carried out laboratory measurements of the airflow in a wind-wavetank, where we deploy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b7ff1871cafe2d5edd933966b68ba1c
https://doi.org/10.5194/egusphere-egu22-7495
https://doi.org/10.5194/egusphere-egu22-7495
Publikováno v:
Flavour and Fragrance Journal. 14:185-190
In continuation of our search for new or uncommon compounds in diverse natural scents we investigated the flower volatiles of Cyclanthus bipartitus Poit., a species of the neotropic family Cyclanthaceae. The structure of the main constituent, represe
Autor:
Katja Schultz, Philip Kraft
Publikováno v:
Journal of Essential Oil Research. 9:509-514
The macrolide fraction of Angelica root oil was analyzed and quantified by GC (coinjection) and GC/MS. ω-Alkanolides C13 (50.0%, [1]), C14 (0.5%, [5]), C15 (42.0%, [2]), C16 (trace, [6]), and C17 (3–5%, [4]) as well as 12-methyl-13-tridecanolide (
Publikováno v:
Chirality. 9:523-528
Autor:
Manfred Hesse, Katja Schultz
Publikováno v:
Tetrahedron. 52:14189-14198
An asymmetric synthesis of the spermidine alkaloid (+)-isocyclocelabenzine (1a) is reported using (3S)-3-amino-3-phenylpropanoic acid as the chiral building block. The 1,2,3,4-tetrahydro-isoquinolin-1-one fragment 9 was synthesized by a modified Bisc
Autor:
Katja Schultz, Manfred Hesse
Publikováno v:
Helvetica Chimica Acta. 79:1295-1304
An asymmetric synthesis of the spermidine alkaloid (+)-cyclocelabenzine (1a) and its (−)-(13S)-epimer 1b is described using optically active (+)-(3S)-3-amino-3-phenylpropionic acid as the chiral building block. The isoquinolin-1-one fragment 15 was
Autor:
Katja Schultz, Manfred Hesse
Publikováno v:
ChemInform. 28
An asymmetric synthesis of the spermidine alkaloid (+)-isocyclocelabenzine (1a) is reported using (3S)-3-amino-3-phenylpropanoic acid as the chiral building block. The 1,2,3,4-tetrahydro-isoquinolin-1-one fragment 9 was synthesized by a modified Bisc
Publikováno v:
ChemInform. 29