Synthetic study of leptosperol A

Author:

Kawamoto YuichiroORCID,Yomura Shin-ichiro,Kobayashi Toyoharu,Ito Hisanaka

Publisher

Elsevier BV

Reference12 articles.

1. Leptosperols A and B, Two Cinnamoylphloroglucinol–Sesquiterpenoid Hybrids from Leptospermum scoparium: Structural Elucidation and Biomimetic Synthesis

2. Total Synthesis of Leptosperol B through Stereocontrolled Intramolecular 1,4-Addition to Construct the Octahydronaphthalene Framework

3. Note on the Preparation of 1,2-Diketones from Acetylenes

4. See Supplementary Material in Detail.

5. Considering that the Z-olefin in 15 was generated as a result of anti-elimination, it is predicted that the stereochemistry of the secondary alcohol at the upper side would be S-configuration: see Supplementary Material in detail. Although it is unknown which is thermodynamically more stable, E or Z olefin on the upper side, we attempted photoisomerization (Z→E) on compound 15, which resulted in decomposition.

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