The Vinylogous Aldol and Related Addition Reactions: Ten Years of Progress | Chemical
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Iodine has been attracting much attention since its discovery in 1811. It is the weakest
oxidizer among the halogens and a poor electrophile that often needs the assistance of a …

Abstract Soft Lewis acid/Brønsted base cooperative catalysts have enabled direct catalytic
asymmetric vinylogous conjugate addition of α, β‐and β, γ‐unsaturated butyrolactones to α …

Benzylidene‐2‐aryl‐4H‐benzo [d][1, 3] oxazines have been synthesized with high
stereoselectivity and regioselectivities from 2‐alkynylbenzamides in the presence of a …

A simple and convenient one-pot multi-component reaction has been described for the
synthesis of functionalized spirolactones. This strategy demonstrated three-component …

Although catalytic asymmetric conjugate addition reactions have remarkably advanced over
the last two decades, the application of less electrophilic α, β‐unsaturated carboxylic acid …

A diastereo-and enantioselective conjugate addition reaction of γ-butenolide with chalcones
has been developed. Notably, unmodified γ-butenolide was directly employed as a …

Efficient reduction of sulfoxides with NaHSO3 catalyzed by I2 - ScienceDirect Skip to main
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Abstract Graphite oxide efficiently promotes the stereoselective Mukaiyama aldol reaction of
2-(trimethylsilyloxy) furan in solvent free conditions assuring a good level of …

The formation of chiral γ‐butenolides has been achieved with good yields (up to 90%), high
enantioselectivity (up to 91%) and diastereoselectivity (up to 9/1, anti‐selective) through an …