Tetrahedron Letters p. 3493 - 3496 (1983)
Update date:2022-08-02
Topics:
Shibasaki
Torisawa
Ikegami
A new prostacyclin analog, 9(o)-methano-Δ6(9α)-PGI1, was synthesized by utilizing intramolecular pinacolic coupling reaction as the key step and was shown to be more potent than carbacyclin in inhibition of platelet aggregation.
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