Author:
Cambie RC,Coddington JM,Rutledge PS,Taylor CM,Woodgate PD
Abstract
2-Oxomanoyl oxide (6) has been converted into 2-oxo-13,14,15,16-tetranorlabd-8(17)-en-12-al (2), an oxygenated analogue of the ambergris odorant, γ-bicyclohomofarnesal (1). The acetoxy acid (10), a key intermediate in the sequence, has been synthesized by an improved route in 75% overall yield from (6).
Cited by
12 articles.
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