A Highly Effective Diels-Alder Approach to cis-Clerodane Natural Products: First Total Synthesis of Solidago Alcohol
ABSTRACT The first total synthesis of solidago alcohol (8) has been achieved in racemic form. The synthetic endeavor takes advantage of a facile and highly face-selective Diels-Alder cycloaddition reaction of cross-conjugated β-keto ester 3, readily accessible from 3-ethoxy-2-cyclohexenone, and TRAN...
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Veröffentlicht in: | Synthesis (Stuttgart) 2004-02, Vol.2004 (2), p.271-275 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | ABSTRACT
The first total synthesis of solidago alcohol (8) has been achieved in racemic form. The synthetic endeavor takes advantage of a facile and highly face-selective Diels-Alder cycloaddition reaction of cross-conjugated β-keto ester 3, readily accessible from 3-ethoxy-2-cyclohexenone, and TRANS-piperylene. |
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ISSN: | 0039-7881 1437-210X |
DOI: | 10.1055/s-2004-815916 |