Abstract
Biologically interesting 9(O)-methano-Δ6-prostaglandin I1 (9(0)-methano-Δ6-PGI1), a chemi-cally stable analog of prostacyclin (PGI2), was efficiently synthesized from 1,3-cyclooctadiene with high stereo- and regiochemical control. In all three biological test systems examined, 9(O)-meth-ano-Δ6-PGI1 was found to be considerably less active than Prostaglandin E1 (PGE1). © 1983, The Pharmaceutical Society of Japan. All rights reserved.
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Iseki, K., Mase, T., Okazaki, T., Shibasaki, M., & Ikegami, S. (1983). Synthesis of. Chemical and Pharmaceutical Bulletin, 31(12), 4448–4455. https://doi.org/10.1248/cpb.31.4448
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