Publication

Total asymmetric synthesis of a new 9,12-anhydroerythronolide aglycone

Pierre Vogel
2002
Journal Articles

Abstract

Two novel, potentially antimicrobial erythronolide aglycon analogs ((-)-9 and (-)-30, respectively), which incorporate a large number of contiguous stereogenic centers, have been prepared by multistep synthesis from simple chirons. The chemistry presented demonstrates the power of the so-called 'naked sugars of the second acneration' approach. As for the sporeamicins, our macrolides are 9,12-anhydroerythronotides, yet presenting a higher degree of complexity due to additional functional groups.

Official source

https://infoscience.epfl.ch/entities/publication/ab6b1d22-0d21-4360-8b5f-fbe9f4a87310

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Pierre Vogel
2002
Journal Articles

Abstract

Official source

https://infoscience.epfl.ch/entities/publication/ab6b1d22-0d21-4360-8b5f-fbe9f4a87310

About this result

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Total asymmetric synthesis of a new 9,12-anhydroerythronolide aglycone

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