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New strategy for the synthesis of the taxane diterpenes formation of the A-ring and introduction of the C-1 hydroxyl group

, : New strategy for the synthesis of the taxane diterpenes formation of the A-ring and introduction of the C-1 hydroxyl group. Tetrahedron Letters 36(30): 5331-5334

The A-ring of the taxanes is conveniently made from an ester-sulfone condensation, and is compatible with the 1-hydroxyl group, thus completing the synthesis of the ABC-rings.


DOI: 10.1016/0040-4039(95)01084-u

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