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The Wieland-MiescherKetone: A Journey from Organocatalysis to Natural Product Synthesis

Ben Bradshaw, +1 more
- 01 Feb 2012 - 
- Vol. 2012, Iss: 03, pp 337-356
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This article is published in Synlett.The article was published on 2012-02-01. It has received 78 citations till now. The article focuses on the topics: Wieland–Miescher ketone.

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Catalytic Enantioselective Desymmetrization Reactions to All-Carbon Quaternary Stereocenters.

TL;DR: The advances in the construction of all-carbon quaternary stereocenters via catalytic enantioselective desymmetrization of prochiral and meso-compounds are summarized and synthetic opportunities still available are outlined.
Journal ArticleDOI

Recent efforts directed to the development of more sustainable asymmetric organocatalysis

TL;DR: This feature article reviews some of the remarkable advancements that have made it possible to develop even more sustainable asymmetric organocatalyzed methodologies.
Journal ArticleDOI

Total Syntheses of Anominine and Tubingensin A

TL;DR: A divergent strategy for the total syntheses of the indole terpenoid anominine and its natural congener tubingensin A has been developed and features a radical deoxygenation followed by an efficient side-chain installation.
Journal ArticleDOI

Asymmetric Supramolecular Catalysis: A Bio-Inspired Tool for the High Asymmetric Induction in the Enamine-Based Michael Reactions

TL;DR: Enantiomerically pure, druglike hexahydroxanthenes with three contiguous stereocenters were synthesized through supramolecular catalysis by D-proline and quinine-NH-thiourea followed by reductive etherification from simple precursors under mild conditions.
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