Page last updated: 2024-08-21

oxazoles and siphonazole

oxazoles has been researched along with siphonazole in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's5 (83.33)29.6817
2010's1 (16.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Eguereva, E; Erol, O; Kehraus, S; Köck, M; König, GM; Krick, A; Nett, M; Neu, E1
Linder, J; Moody, CJ1
Blake, AJ; Linder, J; Moody, CJ1
Ciufolini, MA; Zhang, J1
Chen, J; Ciufolini, MA; Polishchuk, EA; Zhang, J1
Barra, L; Dickschat, JS; Dorrestein, PC; Höver, T; Kaiser, M; Mir Mohseni, M; Schäberle, TF1

Other Studies

6 other study(ies) available for oxazoles and siphonazole

ArticleYear
Siphonazole, an unusual metabolite from Herpetosiphon sp.
    Angewandte Chemie (International ed. in English), 2006, Jun-02, Volume: 45, Issue:23

    Topics: Chloroflexi; Molecular Structure; Oxazoles

2006
The total synthesis of siphonazole, a structurally unusual bis-oxazole natural product.
    Chemical communications (Cambridge, England), 2007, Apr-21, Issue:15

    Topics: Biological Products; Hydrocarbons; Methane; Oxazoles; Rhodium

2007
Total synthesis of siphonazole and its O-methyl derivative, structurally unusual bis-oxazole natural products.
    Organic & biomolecular chemistry, 2008, Nov-07, Volume: 6, Issue:21

    Topics: Biological Products; Oxazoles

2008
Total synthesis of siphonazoles by the use of a conjunctive oxazole building block.
    Organic letters, 2009, Jun-04, Volume: 11, Issue:11

    Topics: Biological Products; Candida albicans; Catalysis; Escherichia coli; Methicillin-Resistant Staphylococcus aureus; Microbial Sensitivity Tests; Molecular Structure; Oxazoles

2009
Development of an oxazole conjunctive reagent and application to the total synthesis of siphonazoles.
    The Journal of organic chemistry, 2009, Dec-04, Volume: 74, Issue:23

    Topics: Biological Products; Indicators and Reagents; Methods; Oxazoles

2009
Discovery of a Mosaic-Like Biosynthetic Assembly Line with a Decarboxylative Off-Loading Mechanism through a Combination of Genome Mining and Imaging.
    Angewandte Chemie (International ed. in English), 2016, 10-17, Volume: 55, Issue:43

    Topics: Antimalarials; Biological Products; Chloroflexi; Data Mining; Decarboxylation; Mass Spectrometry; Multigene Family; Oxazoles

2016