
Journal of Organic Chemistry p. 5826 - 5834 (1991)
Update date:2022-07-30
Topics:
Fisher, Matthew J.
Myers, Cheryl D.
Joglar, Jesus
Chen, Shu-Hui
Danishefsky, Samuel J.
A program directed toward a total synthesis of rapamycin is described.This paper reports the synthesis of enoate 36, a fragment that would correspond to carbons 28-49 of rapamycin.The two building blocks required to reach 36 were allylic alcohol 5 and aci
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Doi:10.1134/S1070363211120127
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