
Tetrahedron Letters p. 8501 - 8504 (1993)
Update date:2022-08-03
Topics:
Ojika, Makoto
Kigoshi, Hideo
Ishigaki, Takeshi
Yamada, Kiyoyuki
By a series of reactions aplyronine A (1) an antitumor substance of marine origin was transformed into six fragments, and their structures were characterized by spectroscopic methods.Relative stereochemistry of four contiguous chiral centers (C29-C32) in 1 was established and that of three contiguous chiral centers (C23-C25) in 1 was deduced on the basis of the 1H NMR spectral analysis of the fragment 8 and the derived acetonide 9, respectively.
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