Synthesis of new .beta.-lactams

C - Chemistry – Metallurgy – 07 – D

Patent

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Details

C07D 305/14 (2006.01) A61K 31/335 (2006.01) C07C 217/58 (2006.01) C07D 205/08 (2006.01)

Patent

CA 2256865

The object of the present invention is the development of new chiral auxiliaries for improved .beta.-lactam formation that control both the diastereoselectivity of .beta.-lactam formation and which can be removed without destruction of the sensitive azetidinone ring, providing valuable intermediates for coupling to the C-13 hydroxyl group of anti-tumour taxanes, such as paclitaxel. Further, the object of the present invention is enantiomerically pure (S)-(-)-1-(p-methoxy-fenyl)propyl-1- amine.

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