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National Institutes of Health
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Teubrevin G and teubrevin H: the first total syntheses of rearranged neo-clerodanes including solutions to the problems of chirality merger and furan ring assembly.
Journal of the American Chemical Society
Corpus ID: 34437685
Total syntheses of teubrevins G (2) and H (3) are described. The reported strategy relies on a highly regioselective…
Enantioselective total syntheses of Teubrevin G and Teubrevin H and studies toward the Enantioselective Total Synthesis of Vinigrol
Corpus ID: 104653121
Total syntheses o f teubrevin G and teubrevin H are described. The successflil approach to these novel diterpenoids involves a…
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