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Efficient and Simple NaBH4 Reduction of Esters at Cationic Micellar Surface

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What this work says

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

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Advanced Organic Chemistry

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Micellar solutions as reaction media

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Convenient methods for the reduction of amides, nitriles, carboxylic esters, acids and hydroboration of alkenes using NaBH4/I2system

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Diastereoselective reduction of E and Z α-alkoxyimino-β-ketoesters by sodium borohydride

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Enantioselective reduction of aryl ketones using LiBH4 and TarB-X: a chiral Lewis acid

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Chemocontrolled reduction of aromatic α-ketoesters by NaBH4: Selective synthesis of α-hydroxy esters or 1,2-diols

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Mechanistic rationale for the NaBH4 reduction of α-keto esters

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Enantioselective synthesis of β-hydroxy esters by Reformatsky reactions in chiral micelles

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Micellar enhancements of rates of SN2 reactions of halide ions: the effect of head group size

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Organic reactivity in microemulsion systems

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The water content of a micelle interior. The fjord vs. reef models

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Secondary valence force catalysis. VII. Catalysis of hydrolysis of p-nitrophenyl hexanoate by micelle-forming cationic detergents

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Organic Reactions Occurring in or on Micelles. I. Reaction Rate Studies of the Alkaline Fading of Triphenylmethane Dyes and Sulfonphthalein Indicators in the Presence of Detergent Salts1

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Reduction of esters to alcohols by means of sodium borohydride in polyethylene glycols

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The Reduction of Esters with Sodium Borohydride1

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A Quantitative Analysis of the Effects of Head Group Bulk on SN2 and E2 Reactions in Cationic Micelles

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Hydrosilylation of Alkynes with a Cationic Rhodium Species Formed in an Anionic Micellar System

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Vesicles Accelerate Proton Transfer from Carbon up to 850-fold

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Stereoselective micelle-promoted ester hydrolysis

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