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- W2800938819 endingPage "7134" @default.
- W2800938819 startingPage "7121" @default.
- W2800938819 abstract "A strategy enabled by C–H and alkene amination technologies for synthesizing the aminocyclitol natural product, pactamycin, is disclosed. This work features two disparate approaches for assembling the five-membered ring core of the target, the first of which utilizes acyl anion catalysis and a second involving β-ketoester aerobic hydroxylation. Installation of the C3–N bond, one of three contiguous nitrogen centers, is made possible through Rh-catalyzed allylic C–H amination of a sulfamate ester. Subsequent efforts are presented to introduce the C1,C2 cis-diamino moiety en route to pactamycin, including carbamate-mediated alkene aziridination. In the course of these studies, assembly of the core of C2-epi-pactamycate, which bears the carbon skeleton and all of the requisite nitrogen and oxygen functional groups found in the natural product, has been achieved." @default.
- W2800938819 created "2018-05-17" @default.
- W2800938819 creator A5004644684 @default.
- W2800938819 creator A5047215672 @default.
- W2800938819 creator A5051474045 @default.
- W2800938819 creator A5066790886 @default.
- W2800938819 date "2018-04-30" @default.
- W2800938819 modified "2023-10-15" @default.
- W2800938819 title "Synthetic Studies Toward Pactamycin Highlighting Oxidative C–H and Alkene Amination Technologies" @default.
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