Chemical Studies on Ambergris
Open Access
- 1 January 1966
- journal article
- Published by Oxford University Press (OUP) in Agricultural and Biological Chemistry
- Vol. 30 (8) , 759-763
- https://doi.org/10.1271/bbb1961.30.759
Abstract
Dihydro-α-ionol (II) was converted to dihydro-α-ionyl bromide (III) and dihydro-α-ionyl tosylate (V), which afforded their Wittig reagents (IV), (VI) on heating with tri-phenylphosphine. The Wittig reaction of ambreinolal-tetrahydropyranylether (VII) with the above Wittig reagents (IV) or (VI) gave a-ambrein-tetrahydropyranylether (VIII).Keywords
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