Hochschulschrift
Funktionalisierte Vinyloxirane durch reduktive Allylierung von Estern : stereoselektive Synthesen von Lamoxiren und Sphingoidbasen
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Maße
-
21 cm
- Umfang
-
III, 202 S.
- Sprache
-
Deutsch
- Anmerkungen
-
Ill., graph. Darst.
Bonn, Univ., Diss., 1999 (Nicht für den Austausch)
- Schlagwort
-
Lamoxiren
Asymmetrische Synthese
Vinyloxirane
Funktionelle Gruppe
Asymmetrische Synthese
- Urheber
- Inhaltsverzeichnis
- Rechteinformation
-
Bei diesem Objekt liegt nur das Inhaltsverzeichnis digital vor. Der Zugriff darauf ist unbeschränkt möglich.
- Letzte Aktualisierung
-
11.06.2025, 14:17 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Objekttyp
- Hochschulschrift
Beteiligte
Ähnliche Objekte (12)
Photosensitizers Enable the Formation of Biphenyls with UV‐LEDs and Sunlight
Novel Biocatalysts from Specialized Metabolism
Novel Biocatalysts from Specialized Metabolism
Loss of Single‐Domain Function in a Modular Assembly Line Alters the Size and Shape of a Complex Polyketide
Thiotemplated Biosynthesis of Bacterial Polyyne Fatty Acids by a Designated Desaturase Triad
A Photochemical Macrocyclization Route to Asymmetric Strained (3.2) Paracyclophanes
A Type III Polyketide Synthase Specific for Sporulating Negativicutes is Responsible for Alkylpyrone Biosynthesis
Bacterial Isothiocyanate Biosynthesis by Rhodanese‐Catalyzed Sulfur Transfer onto Isonitriles
An Enzymatic Prodrug‐like Route to Thio and Selenoamides
Novel Biocatalysts from Specialized Metabolism
An Enzymatic Prodrug‐like Route to Thio and Selenoamides
Genome mining for ribosomally synthesized and post-translationally modified peptides (RiPPs) in anaerobic bacteria
Photosensitizers Enable the Formation of Biphenyls with UV‐LEDs and Sunlight
Novel Biocatalysts from Specialized Metabolism
Novel Biocatalysts from Specialized Metabolism
Loss of Single‐Domain Function in a Modular Assembly Line Alters the Size and Shape of a Complex Polyketide
Thiotemplated Biosynthesis of Bacterial Polyyne Fatty Acids by a Designated Desaturase Triad
A Photochemical Macrocyclization Route to Asymmetric Strained (3.2) Paracyclophanes
A Type III Polyketide Synthase Specific for Sporulating Negativicutes is Responsible for Alkylpyrone Biosynthesis
Bacterial Isothiocyanate Biosynthesis by Rhodanese‐Catalyzed Sulfur Transfer onto Isonitriles
An Enzymatic Prodrug‐like Route to Thio and Selenoamides
Novel Biocatalysts from Specialized Metabolism
An Enzymatic Prodrug‐like Route to Thio and Selenoamides
Genome mining for ribosomally synthesized and post-translationally modified peptides (RiPPs) in anaerobic bacteria
Photosensitizers Enable the Formation of Biphenyls with UV‐LEDs and Sunlight
Novel Biocatalysts from Specialized Metabolism
Novel Biocatalysts from Specialized Metabolism
Loss of Single‐Domain Function in a Modular Assembly Line Alters the Size and Shape of a Complex Polyketide
Thiotemplated Biosynthesis of Bacterial Polyyne Fatty Acids by a Designated Desaturase Triad
A Photochemical Macrocyclization Route to Asymmetric Strained (3.2) Paracyclophanes
A Type III Polyketide Synthase Specific for Sporulating Negativicutes is Responsible for Alkylpyrone Biosynthesis
Bacterial Isothiocyanate Biosynthesis by Rhodanese‐Catalyzed Sulfur Transfer onto Isonitriles
An Enzymatic Prodrug‐like Route to Thio and Selenoamides
Novel Biocatalysts from Specialized Metabolism
An Enzymatic Prodrug‐like Route to Thio and Selenoamides