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Cascade Michael Addition/Cycloketalization of Cyclic 1,3-Dicarbonyl Compounds: Important Role of the Tethered Alcohol of α,β-Unsaturated Carbonyl Compounds on Reaction Rate and Regioselectivity

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Highly Enantioselective Michael Addition of Cyclic 1,3‐Dicarbonyl Compounds to α,β‐Unsaturated Ketones.

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Utilisation of 1,3‐Dicarbonyl Derivatives in Multicomponent Reactions

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Organocatalytic Enantioselective Michael Addition of 4‐Hydroxycoumarin to α,β‐Unsaturated Ketones: A Simple Synthesis of Warfarin

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Recent progress in the development of coumarin derivatives as potent anti‐HIV agents

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Total synthesis of (+)-xyloketal D, a secondary metabolite from the mangrove fungus Xylaria sp.

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Ring-closure reactions. 22. Kinetics of cyclization of diethyl (.omega.-bromoalkyl)malonates in the range of 4- to 21-membered rings. Role of ring strain

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Photochemical rearrangements of .alpha.-methylene ketones

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4-Hydroxy-6-alkyl-2-pyrones as nucleophilic coupling partners in Mitsunobu reactions and oxa-Michael additions

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What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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