Evolution of a cycloaddition-rearrangement approach to the squalestatins: a quarter-century odyssey
The highs, lows, and diversions of a journey leading to two syntheses of 6,7-dideoxysqualestatin H5 is described. Both syntheses relied on highly diastereoselective n -alkylations of a tartrate acetonide enolate and subsequent oxidation-hydrolysis to provide an asymmetric entry to β-hydrox...
Main Authors: | Almohseni, HAA, Hodgson, DM |
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格式: | Journal article |
语言: | English |
出版: |
Thieme Publishing
2020
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