SciELO

Reaction of acyclic enaminones with methoxymethylene meldrum's acid: synthetic and structural implications

The reaction of acyclic enaminones with methoxymethylene Meldrum's acid afforded N-adduct and/or C-adduct of enaminones in moderate to good yields. The regiochemistry of this reaction depends on the N ...
Nature

Switching Sides: Regiochemistry and Functionalization Dictate the Photoswitching Properties of Imines

The Nature Index 2024 Research Leaders — previously known as Annual Tables — reveal the leading institutions and countries/territories in the natural and health sciences, according to their output in ...
Scientific Research Publishing

B. J. Shorthill and T. E. Glass, “Naphthalene Based Calixarenes: Unusual Regiochemistry of a Friedel-Crafts Alkylation,” Organic Letters, Vol. 3, No. 4, 2001, pp. 577-579 ...

ABSTRACT: A number of doubly-fused [1,2] naphthodifurans have been synthesized from the corresponding diallyl-dihydroxy naphthalene precursors involving N-iodosuccinimide in acetonitrile and also by ...
C&EN

Cooperativity of Regiochemistry Control Strategies in Reductive Couplings of Propargyl Alcohols and Aldehydes

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C&EN

Regiochemistry in cycloadditions of diazomethane to thioformaldehyde and thioketones

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