Organic Letters 2012-01-20

Diisobutylaluminum hydride reductions revitalized: a fast, robust, and selective continuous flow system for aldehyde synthesis.

Damien Webb, Timothy F Jamison

Index: Org. Lett. 14(2) , 568-71, (2012)

Full Text: HTML

Abstract

A continuous flow system for the multiparameter (flow rate, temperature, residence time, stoichiometry) optimization of the DIBALH reduction of esters to aldehydes is described. Incorporating an in-line quench (MeOH), these transformations are generally complete in fewer than 60 s. Mixing of the DIBALH and ester solutions was observed to be an exceptionally critical parameter for optimum results. This system thus provides general guidelines based on the structure of the ester for selective reduction of an ester without overreduction.© 2011 American Chemical Society


Related Compounds

  • Diisobutylaluminiu...

Related Articles:

Use of multivariate statistical techniques to optimize the separation of 17 capsinoids by ultra performance liquid chromatography using different columns.

2015-03-01

[Talanta 134 , 256-63, (2015)]

[Development of domino reactions based on skeletal rearrangement].

2011-01-01

[Yakugaku Zasshi 131(11) , 1563-73, (2011)]

DIBAL-mediated reductive transformation of trans-dimethyl tartrate acetonide into ε-hydroxy α,β-unsaturated ester and its derivatives.

2011-06-03

[J. Org. Chem. 76(11) , 4669-74, (2011)]

Lactone-free ginkgolides via regioselective DIBAL-H reduction.

2005-10-07

[Org. Biomol. Chem. 3(19) , 3471-2, (2005)]

DIBALH mediated reduction of the acetal moiety on perhydrofuro[2,3-b]pyran derivatives.

2001-09-21

[Carbohydr. Res. 335(1) , 63-70, (2001)]

More Articles...