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SYNTHESIS OF (±)-COSTUNOLIDE, AN ANTITUMOR GERMACRANOLIDE, FROM E,E-FARNESOL BY USE OF A LOW-VALENT CHROMIUM REAGENT
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Stereospecific synthesis of 2,7-dimethyl-trans,trans-2,6-octadiene-1,8-dial, a tail-to-tail all-trans bifunctional isoprenoid synthetic unit. Convenient synthesis of squalene
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The Total Synthesis of Dihydrocostunolide
inferredcites →https://doi.org/10.1021/jo00430a010openalex-snapshot
Total synthesis of (+)-costunolide
inferredcites →https://doi.org/10.1021/jo01273a004openalex-snapshot
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A rapid, mild procedure for the preparation of alkyl chlorides and bromides
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Highly Selective Carbon-Carbon Bond Forming Reactions Mediated by Chromium(II) Reagents
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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ChemInform Abstract: Synthesis of (±)‐Costunolide (I), an Antitumor Germacranolide, from E,E‐Farnesol by Use of a Low‐Valent Chromium Reagent.
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1,4-asymmetric induction in the Nozaki-Hiyama reaction
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