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(E)-beta-Borylstyrene in the Diels-Alder Reaction with 3,5-Dibromo-2-pyrone for the Syntheses of (+/-)-1-epi-Pancratistatin and (+/-)- Pancratistatin

Authors
Cho, Hyun-KyuLim, Hwa-YeonCho, Cheon-Gyu
Issue Date
Nov-2013
Publisher
AMER CHEMICAL SOC
Citation
ORGANIC LETTERS, v.15, no.22, pp.5806 - 5809
Indexed
SCIE
SCOPUS
Journal Title
ORGANIC LETTERS
Volume
15
Number
22
Start Page
5806
End Page
5809
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/143659
DOI
10.1021/ol4028623
ISSN
1523-7060
Abstract
New synthetic routes to (+/-)-1-epi-pancratistatin and (+/-)-pancratistatin were devised using (E)-beta-borylstyrene as a dienophile for the key Diels-Alder reaction with 3,5-dibromo-2-pyrone. The boronate in the cycloadduct was oxidized to provide the pivotal C1-hydroxyl group of the titled compounds.
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