Polycyclic framework synthesis of anominine and tubingensin A indole diterpenoids
Decalin
Methylene
Methyl Ketone
DOI:
10.1039/b718280e
Publication Date:
2008-01-18T11:00:15Z
AUTHORS (3)
ABSTRACT
A highly congested decalin embodying an α-methylene ketone is synthesized in 11 steps from the Wieland–Miescher and efficiently converted to polycyclic frameworks of anominine tubingensin A, which constitutes first approach skeleton these indole diterpenoids.
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