Abstract
A concise synthesis of litseaones A and B, which were isolated from the stem barks of Litsea rubescens and L. pedunculata, is described in this study. Litseaone A was synthesized in just three steps from a known phloroglucinol derivative. The direct conversion of litseaone A into litseaone B was also achieved.
Original language | English |
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Pages (from-to) | 810-812 |
Number of pages | 3 |
Journal | Bioscience, Biotechnology and Biochemistry |
Volume | 83 |
Issue number | 5 |
DOIs | |
Publication status | Published - 2019 Jan 1 |
Externally published | Yes |
Keywords
- Cytotoxic
- Litseaones A and B
- Protecting-group-free
- Synthesis
ASJC Scopus subject areas
- Biotechnology
- Analytical Chemistry
- Biochemistry
- Applied Microbiology and Biotechnology
- Molecular Biology
- Organic Chemistry