Tetrahedron Letters p. 4231 - 4232 (1994)
Update date:2022-08-16
Topics:
Sharma
Rao, S. Mahender
A stereoselective total synthesis of (11R,12S)-diHETE is described. The strategy is based on the use of a 'sugar' derived 'chiron' for the incorporation of vic-diol' stereocentres, while Wittig reactions for the assembly of requisite carbon frame work of the target molecule.
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