Publisher: Wiley

Issue: 41

License: [{"start"=>{"date-parts"=>[[2020, 8, 11]], "date-time"=>"2020-08-11T00:00:00Z", "timestamp"=>1597104000000}, "content-version"=>"vor", "delay-in-days"=>0, "URL"=>"http://creativecommons.org/licenses/by/4.0/"}]

Publication date(s): 2020/10/05 (print) 2020/08/11 (online)

Pages: 18156-18160

Volume: 59 Issue: 41

Journal: Angewandte Chemie International Edition

Link: [{"URL"=>"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fanie.202006246", "content-type"=>"application/pdf", "content-version"=>"vor", "intended-application"=>"text-mining"}, {"URL"=>"https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.202006246", "content-type"=>"application/pdf", "content-version"=>"vor", "intended-application"=>"text-mining"}, {"URL"=>"https://onlinelibrary.wiley.com/doi/full-xml/10.1002/anie.202006246", "content-type"=>"application/xml", "content-version"=>"vor", "intended-application"=>"text-mining"}, {"URL"=>"https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.202006246", "content-type"=>"unspecified", "content-version"=>"vor", "intended-application"=>"similarity-checking"}]

AbstractThe combination of biocatalysis and chemo‐catalysis increasingly offers chemists access to more diverse chemical architectures. Here, we describe the combination of a toolbox of chiral‐amine‐producing biocatalysts with a Buchwald–Hartwig cross‐coupling reaction, affording a variety of α‐chiral aniline derivatives. The use of a surfactant allowed reactions to be performed sequentially in the same flask, preventing the palladium catalyst from being inhibited by the high concentrations of ammonia, salts, or buffers present in the aqueous media in most cases. The methodology was further extended by combining with a dual‐enzyme biocatalytic hydrogen‐borrowing cascade in one pot to allow for the conversion of a racemic alcohol to a chiral aniline.

There are no objects associated to this publication