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Stereoselective Synthesis of (E)-Tagetone

✍ Scribed by Kunz, Joachim ;Breitmaier, Eberhard

Publisher: John Wiley and Sons
Year: 1995
Tongue: English
Weight: 147 KB
Volume: 1995
Category: Article
ISSN: 0947-3440
DOI: 10.1002/jlac.1995199504102

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✦ Synopsis

Tagetes glundulifera I (E)-Tagetone I 1,3-Dithiane I Oxopropylenation / Wittig alkylenation (E)-Tagetone (8) was prepared in four steps by successive alkylation of 1,3-dithiane (1) by 1-iodo-2-methylpropane ( 2 ) and by 3-ethoxy-2-methylacrolein (3), followed by treatment

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