Expanding the Synthetic Toolbox through Metal–Enzyme Cascade Reactions

The combination of metal-, photo-, enzyme-, and/or organocatalysis provides multiple synthetic solutions, especially when the creation of chiral centers is involved. Historically, enzymes and transition metal species have been exploited simultaneously through dynamic kinetic resolutions of racemates...

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Published in:Chemical reviews Vol. 123; no. 9; pp. 5297 - 5346
Main Authors: González-Granda, Sergio, Albarrán-Velo, Jesús, Lavandera, Iván, Gotor-Fernández, Vicente
Format: Journal Article
Language:English
Published: United States American Chemical Society 10-05-2023
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Abstract The combination of metal-, photo-, enzyme-, and/or organocatalysis provides multiple synthetic solutions, especially when the creation of chiral centers is involved. Historically, enzymes and transition metal species have been exploited simultaneously through dynamic kinetic resolutions of racemates. However, more recently, linear cascades have appeared as elegant solutions for the preparation of valuable organic molecules combining multiple bioprocesses and metal-catalyzed transformations. Many advantages are derived from this symbiosis, although there are still bottlenecks to be addressed including the successful coexistence of both catalyst types, the need for compatible reaction media and mild conditions, or the minimization of cross-reactivities. Therefore, solutions are here also provided by means of catalyst coimmobilization, compartmentalization strategies, flow chemistry, etc. A comprehensive review is presented focusing on the period 2015 to early 2022, which has been divided into two main sections that comprise first the use of metals and enzymes as independent catalysts but working in an orchestral or sequential manner, and later their application as bionanohybrid materials through their coimmobilization in adequate supports. Each part has been classified into different subheadings, the first part based on the reaction catalyzed by the metal catalyst, while the development of nonasymmetric or stereoselective processes was considered for the bionanohybrid section.
AbstractList The combination of metal-, photo-, enzyme-, and/or organocatalysis provides multiple synthetic solutions, especially when the creation of chiral centers is involved. Historically, enzymes and transition metal species have been exploited simultaneously through dynamic kinetic resolutions of racemates. However, more recently, linear cascades have appeared as elegant solutions for the preparation of valuable organic molecules combining multiple bioprocesses and metal-catalyzed transformations. Many advantages are derived from this symbiosis, although there are still bottlenecks to be addressed including the successful coexistence of both catalyst types, the need for compatible reaction media and mild conditions, or the minimization of cross-reactivities. Therefore, solutions are here also provided by means of catalyst coimmobilization, compartmentalization strategies, flow chemistry, etc. A comprehensive review is presented focusing on the period 2015 to early 2022, which has been divided into two main sections that comprise first the use of metals and enzymes as independent catalysts but working in an orchestral or sequential manner, and later their application as bionanohybrid materials through their coimmobilization in adequate supports. Each part has been classified into different subheadings, the first part based on the reaction catalyzed by the metal catalyst, while the development of nonasymmetric or stereoselective processes was considered for the bionanohybrid section.
Author Gotor-Fernández, Vicente
Albarrán-Velo, Jesús
González-Granda, Sergio
Lavandera, Iván
AuthorAffiliation Organic and Inorganic Chemistry Department
AuthorAffiliation_xml – name: Organic and Inorganic Chemistry Department
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  givenname: Sergio
  surname: González-Granda
  fullname: González-Granda, Sergio
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  fullname: Albarrán-Velo, Jesús
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  givenname: Iván
  orcidid: 0000-0003-4857-4428
  surname: Lavandera
  fullname: Lavandera, Iván
  email: lavanderaivan@uniovi.es
– sequence: 4
  givenname: Vicente
  orcidid: 0000-0002-9998-0656
  surname: Gotor-Fernández
  fullname: Gotor-Fernández, Vicente
  email: vicgotfer@uniovi.es
BackLink https://www.ncbi.nlm.nih.gov/pubmed/36626572$$D View this record in MEDLINE/PubMed
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SecondaryResourceType review_article
Snippet The combination of metal-, photo-, enzyme-, and/or organocatalysis provides multiple synthetic solutions, especially when the creation of chiral centers is...
SourceID proquest
crossref
pubmed
acs
SourceType Aggregation Database
Index Database
Publisher
StartPage 5297
SubjectTerms Cascade chemical reactions
Catalysts
Chemical reactions
Coimmobilization
Enzymes
Metals
Organic chemistry
Stereoselectivity
Symbiosis
Transition metals
Title Expanding the Synthetic Toolbox through Metal–Enzyme Cascade Reactions
URI http://dx.doi.org/10.1021/acs.chemrev.2c00454
https://www.ncbi.nlm.nih.gov/pubmed/36626572
https://www.proquest.com/docview/2812081378
https://search.proquest.com/docview/2774596877
Volume 123
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