Alkoxyallene-Based Stereodivergent Syntheses of (−)-Hyacinthacine B4 and of Putative Hyacinthacine C5 Epimers: Proposal of Hyacinthacine C5 Structure
Author:
Affiliation:
1. Department of Chemistry “Ugo Schiff”, University of Firenze, Via della Lastruccia 3-13, 50019 Sesto Fiorentino, Italy
2. Institut für Chemie und Biochemie, Freie Universität Berlin, Takustrasse 3, 14195 Berlin, Germany
Funder
Deutsche Forschungsgemeinschaft
Bayer HealthCare
Ministero dell'Istruzione, dell'Universit?? e della Ricerca
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.7b00667
Reference40 articles.
1. Iminosugars
2. Cycloadditions of Sugar-Derived Nitrones Targeting Polyhydroxylated Indolizidines
3. Polyhydroxyamino-Piperidine-Type Iminosugars and Pipecolic Acid Analogues from aD-Mannose-Derived Aldehyde
4. Synthesis and Glycosidase Inhibition Studies of 5-Methyl-Substituted Tetrahydroxyindolizidines and -pyrrolizidines Related to Natural Hyacinthacines B
5. Total Synthesis of (+)-Hyacinthacine A1, (+)-7a-epi-Hyacinthacine A1, (6R)-6-Hydroxyhyacinthacine A1 and (6S)-6-Hydroxy-7a-epi-hyacinthacine A1
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