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Methods for obtaining optically active intermediates for prostaglandin synthesis [review]

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Pharmaceutical Chemistry Journal Aims and scope

Conclusion

Thus, obtaining chiral precursors of prostaglandins has been described in the literature using most of the familiar enantioselective synthesis methods. At the same time, the large number of the techniques used makes it possible to draw the conclusion that there is no single universal method for obtaining enantiomerically pure prostaglandin intermediates. Therefore the search for new approaches to obtaining optically active intermediates for prostaglandin synthesis remains timely even today.

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  1. Vitaminy Scientific-Industrial Association, Moscow

    V. L. Khristoforov & V. A. Serebryanyi

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Translated from Khimiko-farmatsevticheskii Zhurnal, Vol. 28, No. 6, pp. 36–59, June, 1994.

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Khristoforov, V.L., Serebryanyi, V.A. Methods for obtaining optically active intermediates for prostaglandin synthesis [review]. Pharm Chem J 28, 412–440 (1994). https://doi.org/10.1007/BF02285402

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