Establishing Consensus Stereostructures for the Naphthoquinonopyrano-γ-lactone Natural Products (-)-Arizonin B1 and (-)-Arizonin C1 by Total Syntheses. Diastereocontrol of Oxa-Pictet-Spengler Cyclizations by Protective-Group Optimization-Reference-Cited by-同舟云学术

Establishing Consensus Stereostructures for the Naphthoquinonopyrano-γ-lactone Natural Products (-)-Arizonin B1 and (-)-Arizonin C1 by Total Syntheses. Diastereocontrol of Oxa-Pictet-Spengler Cyclizations by Protective-Group Optimization

Published:2017-05-03 Issue:17 Volume:2017 Page:2512-2539
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Neumeyer Markus¹,Brückner Reinhard¹^ORCID

Affiliation:

1. Institut für Organische Chemie; Albert-Ludwigs-Universität Freiburg; Albertstraße 21 79104 Freiburg Germany

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference148 articles.

1. Synthetic Strategies Towards Pyranonaphthoquinone Antibiotics

2. Total Synthesis of Selected Bioactive Natural Products: Illustration of Strategy and Design

3. Total syntheses of bioactive natural products from carbohydrates

4. Pyranonaphthoquinones—isolation, biological activity and synthesis

5. Total synthesis of the big four antibiotics and related antibiotics

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