Abstract
The title macrosphelides were synthesized by using two-step conversion of furans into γ-oxo-α,β- unsaturated carboxylic acids as a key step. In the case of macrosphelide H, AcCH2 group at C(3) was constructed from CH2=CHCH2 by Wacker oxidation under modified conditions.
Keywords: macrosphelide, asymmetric synthesis, wacker oxidation, furan, furan oxidation
Letters in Organic Chemistry
Title: Total Syntheses of Macrosphelides C, F, G and H
Volume: 1 Issue: 4
Author(s): Yuichi Kobayashi, Yong-Gang Wang and Hukum P. Acharya
Affiliation:
Keywords: macrosphelide, asymmetric synthesis, wacker oxidation, furan, furan oxidation
Abstract: The title macrosphelides were synthesized by using two-step conversion of furans into γ-oxo-α,β- unsaturated carboxylic acids as a key step. In the case of macrosphelide H, AcCH2 group at C(3) was constructed from CH2=CHCH2 by Wacker oxidation under modified conditions.
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Cite this article as:
Kobayashi Yuichi, Wang Yong-Gang and Acharya P. Hukum, Total Syntheses of Macrosphelides C, F, G and H, Letters in Organic Chemistry 2004; 1 (4) . https://dx.doi.org/10.2174/1570178043400424
DOI https://dx.doi.org/10.2174/1570178043400424 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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