Literature DB >> 32440038

Synthetic utility of one-pot chemoenzymatic reaction sequences.

Tyler J Doyon1,2, Alison R H Narayan1,2,3.   

Abstract

In recent years, there has been a rapid and sustained increase in the development and use of one-pot chemoenzymatic reaction processes for the efficient synthesis of high-value molecules. This strategy can provide a number of advantages over traditional synthetic methods, including high levels of selectivity in reactions, mild and sustainable reaction conditions, and the ability to rapidly build molecular complexity in a single reaction vessel. Here, we present several examples of chemoenzymatic one-pot reaction sequences that demonstrate the diversity of transformations that can be incorporated in these processes.

Entities:  

Keywords:  biocatalysis; chemoenzymatic; one-pot process

Year:  2019        PMID: 32440038      PMCID: PMC7241462          DOI: 10.1055/s-0037-1611848

Source DB:  PubMed          Journal:  Synlett        ISSN: 0936-5214            Impact factor:   2.454


  27 in total

1.  Concise, stereoselective route to the four diastereoisomers of 4-methylproline.

Authors:  Annabel C Murphy; Maya I Mitova; John W Blunt; Murray H G Munro
Journal:  J Nat Prod       Date:  2008-04-17       Impact factor: 4.050

2.  Cooperative asymmetric reactions combining photocatalysis and enzymatic catalysis.

Authors:  Zachary C Litman; Yajie Wang; Huimin Zhao; John F Hartwig
Journal:  Nature       Date:  2018-08-15       Impact factor: 49.962

3.  Chemo-enzymatic synthesis of pharmaceutical intermediates.

Authors:  Ramesh N Patel
Journal:  Expert Opin Drug Discov       Date:  2008-02       Impact factor: 6.098

4.  Cooperative tandem catalysis by an organometallic complex and a metalloenzyme.

Authors:  Carl A Denard; Hua Huang; Mark J Bartlett; Lu Lu; Yichen Tan; Huimin Zhao; John F Hartwig
Journal:  Angew Chem Int Ed Engl       Date:  2014-01-07       Impact factor: 15.336

Review 5.  Transition metal catalysis-a unique road map in the stereoselective synthesis of 1,3-polyols.

Authors:  Pradeep Kumar; Divya Tripathi; Brijesh M Sharma; Namrata Dwivedi
Journal:  Org Biomol Chem       Date:  2017-01-25       Impact factor: 3.876

Review 6.  Biocatalysis for the synthesis of pharmaceuticals and pharmaceutical intermediates.

Authors:  Huihua Sun; Hongfang Zhang; Ee Lui Ang; Huimin Zhao
Journal:  Bioorg Med Chem       Date:  2017-06-28       Impact factor: 3.641

7.  Peniphenone and Penilactone Formation in Penicillium crustosum via 1,4-Michael Additions of ortho-Quinone Methide from Hydroxyclavatol to γ-Butyrolactones from Crustosic Acid.

Authors:  Jie Fan; Ge Liao; Florian Kindinger; Lena Ludwig-Radtke; Wen-Bing Yin; Shu-Ming Li
Journal:  J Am Chem Soc       Date:  2019-03-04       Impact factor: 15.419

8.  Iterative approach to polyketide-type structures: stereoselective synthesis of 1,3-polyols utilizing the catalytic asymmetric Overman esterification.

Authors:  Jörg T Binder; Stefan F Kirsch
Journal:  Chem Commun (Camb)       Date:  2007-08-06       Impact factor: 6.222

9.  Chiral aryl iodide catalysts for the enantioselective synthesis of para-quinols.

Authors:  Kelly A Volp; Andrew M Harned
Journal:  Chem Commun (Camb)       Date:  2013-04-14       Impact factor: 6.222

10.  A chemo-enzymatic route to enantiomerically pure cyclic tertiary amines.

Authors:  Colin J Dunsmore; Reuben Carr; Toni Fleming; Nicholas J Turner
Journal:  J Am Chem Soc       Date:  2006-02-22       Impact factor: 15.419

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