Three rings in one step: A quick approach to IKD-8344
A highly efficient enantioselective total synthesis of the natural antibiotic IKD-8344 is achieved through a convergent route. This route features an otherwise impossible concurrent formation of the THF rings from a linear polyketide precursor through intramolecular O alkylations of mesylates in competition with normally rather facile β elimination and/or α racemization reactions (see scheme, Ms=methanesulfonyl). Copyright
Zou, Yang,Wu, Yikang
p. 4968 - 4971
(2012/06/30)
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