| Literature DB >> 21958106 |
Bo Bi1, Richard Y-C Huang, Karl Maurer, Ceng Chen, Kevin D Moeller.
Abstract
A "safety-catch" linker strategy has been used to release a portion of the products of a Diels-Alder reaction conducted on a microelectrode array for characterization of stereochemistry. The attachment and cleavage of organic compounds from the surface of selected electrodes in the array can be accomplished by site-selective generation of base or acid at the electrode. It was found that the surface of the array had a minor influence on the stereochemistry of the Diels-Alder reaction, leading to slightly more of the exo-product relative to a similar solution-phase reaction.Entities:
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Year: 2011 PMID: 21958106 PMCID: PMC3947835 DOI: 10.1021/jo2017907
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354