Literature DB >> 12412063

Modern separation techniques for the efficient workup in organic synthesis.

Carl Christoph Tzschucke1, Christian Markert, Willi Bannwarth, Sebastian Roller, André Hebel, Rainer Haag.   

Abstract

The shift of paradigm in combinatorial chemistry, from large compound libraries (of mixtures) on a small scale towards defined compound libraries where each compound is prepared in an individual well, has stimulated the search for alternative separation approaches. The key to a rapid and efficient synthesis is not only the parallel arrangement of reactions, but simple work-up procedures so as to circumvent time-consuming and laborious purification steps. During the initial development stages of combinatorial synthesis it was believed that rational synthesis of individual compounds could only be achieved by solid-phase strategies. However, there are a number of problems in solid-phase chemistry: most notably there is the need for a suitable linker unit, the limitation of the reaction conditions to certain solvents and reagents, and the heterogeneous reaction conditions. Further disadvantages are: the moderate loading capacities of the polymeric support and the limited stability of the solid support. In the last few years several new separation techniques have been developed. Depending on the chemical problem or the class of compounds to be prepared, one can choose from a whole array of different approaches. Most of these modern separation approaches rely on solution-phase chemistry, even though some of them use solid-phase resins as tools (for example, as scavengers). Several of these separation techniques are based on liquid-liquid phase separation, including ionic liquids, fluorous phases, and supercritical solvents. Besides being benign with respect to their environmental aspects, they also show a number of advantages with respect to the work-up procedures of organic reactions as well as simplicity in the isolation of products. Another set of separation strategies involves polymeric supports (for example, as scavengers or for cyclative cleavage), either as solid phases or as soluble polymeric supports. In contrast to solid-phase resins, soluble polymeric supports allow reactions to be performed under homogeneous conditions, which can be an important factor in catalysis. At the same time, a whole set of techniques has been developed for the separation of these soluble polymeric supports from small target molecules. Finally, miscellaneous separation techniques, such as phase-switchable tags for precipitation by chemical modification or magnetic beads, can accelerate the separation of compounds in a parallel format.

Year:  2002        PMID: 12412063     DOI: 10.1002/1521-3773(20021104)41:21<3964::AID-ANIE3964>3.0.CO;2-3

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  25 in total

Review 1.  Fluorous synthesis of heterocyclic systems.

Authors:  Wei Zhang
Journal:  Chem Rev       Date:  2004-05       Impact factor: 60.622

2.  Rapid deprotection of N-Boc amines by TFA combined with freebase generation using basic ion-exchange resins.

Authors:  Natarajan Srinivasan; Alexander Yurek-George; A Ganesan
Journal:  Mol Divers       Date:  2005       Impact factor: 2.943

3.  Microwave-assisted synthesis of a 3-aminoimidazo[1,2-a]-pyridine/pyrazine library by fluorous multicomponent reactions and subsequent cross-coupling reactions.

Authors:  Yimin Lu; Wei Zhang
Journal:  QSAR Comb Sci       Date:  2004

4.  Synthetic applications of fluorous solid-phase extraction (F-SPE).

Authors:  Wei Zhang; Dennis P Curran
Journal:  Tetrahedron       Date:  2006-12-18       Impact factor: 2.457

5.  Plate-to-plate fluorous solid-phase extraction for solution-phase parallel synthesis.

Authors:  Wei Zhang; Yimin Lu; Tadamichi Nagashima
Journal:  J Comb Chem       Date:  2005 Nov-Dec

6.  Fluorous 2-Chloropyridinium Salt (Mukaiyama Condensation Reagent) for Amide Formation Reactions.

Authors:  Tadamichi Nagashima; Yimin Lu; Michael J Petro; Wei Zhang
Journal:  Tetrahedron Asymmetry       Date:  2005-09-19

7.  A highly efficient microwave-assisted suzuki coupling reaction of aryl perfluorooctylsulfonates with boronic acids.

Authors:  Wei Zhang; Christine Hiu-Tung Chen; Yimin Lu; Tadamichi Nagashima
Journal:  Org Lett       Date:  2004-04-29       Impact factor: 6.005

8.  Sequence-Defined Oligomers from Hydroxyproline Building Blocks for Parallel Synthesis Applications.

Authors:  Rosemary L Kanasty; Arturo J Vegas; Luke M Ceo; Martin Maier; Klaus Charisse; Jayaprakash K Nair; Robert Langer; Daniel G Anderson
Journal:  Angew Chem Int Ed Engl       Date:  2016-07-01       Impact factor: 15.336

9.  Investigations into the use of a polyfluorooctanol as an auxiliary component for an aldol reaction.

Authors:  Jason Eames; Hasina Khanom
Journal:  Molecules       Date:  2004-04-30       Impact factor: 4.411

10.  Fluorous 2,4-Dichloro-1,3,5-triazine (F-DCT) as Amide Coupling Agent.

Authors:  Wei Zhang; Yimin Lu
Journal:  QSAR Comb Sci       Date:  2006-07-11
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