Dibromo-2-pyrone underwent facile Diels-Alder [4+2] cycloadditions with cycloalkenyl silyl ethers to provide a series of tricyclolactones, with good to excellent chemical yields and stereoselectivity. The resulting cycloadducts could be readily converted into the corresponding bicarbocycles upon sel
β-Silyl Styrene As a Dienophile in the Cycloaddition with 3,5-Dibromo-2-pyrone for the Total Synthesis of (±)-Pancratistatin
✍ Scribed by Kang, Ho-Ung; Cho, Hyun-Kyu; Cho, Cheon-Gyu; Jung, Yong-Geun
- Book ID
- 115452708
- Publisher
- American Chemical Society
- Year
- 2011
- Tongue
- English
- Weight
- 756 KB
- Volume
- 13
- Category
- Article
- ISSN
- 1523-7060
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