Literature DB >> 28691061

An Enlightening Reactor.

Daniel K Kim1, Vy M Dong1.   

Abstract

Entities:  

Year:  2017        PMID: 28691061      PMCID: PMC5492411          DOI: 10.1021/acscentsci.7b00218

Source DB:  PubMed          Journal:  ACS Cent Sci        ISSN: 2374-7943            Impact factor:   14.553


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In recent years, the reaction vessel by which chemists perform organic reactions has undergone major changes. No longer limited to round-bottom flasks, we can perform experiments in microwave ovens, flow reactors,[1−3] and 96-well plates.[4,5] Each of these technologies has enabled breakthroughs in organic synthesis not easily achieved using conventional flasks. In the rapid development of photoredox technology, a gap in physical technology has led to a wide range of protocols that use different light sources.[6] A standard, affordable reactor that is easy to use would accelerate the use of photoredox methodology. To address this, a collaboration between Merck researchers and the MacMillan laboratory at Princeton has produced an integrated photoreactor built with a modular design (Figure ).[7]
Figure 1

A simple modular design for an LED powered photoreactor. Reprinted with permission from ref (7). Copyright 2017 American Chemical Society.

A simple modular design for an LED powered photoreactor. Reprinted with permission from ref (7). Copyright 2017 American Chemical Society. The simple and elegant design allows for efficient catalysis of photoredox reactions. A sampling of top pharmaceutical photoredox coupling reactions were tested with the new integrated photoreactor. In general, the small-scale photoreactor could be employed broadly. The new photoreactor enables rate accelerations between 2 to 20 times when evaluating various photoredox transformations using a 360° light source. The designer photoreactor could also precisely control the LED output power, a parameter previously challenging to control. The silyl-mediated cross-electrophilic cross-coupling reaction was sensitive to the buildup of hydrobromic acid at the maximum LED output level (Figure ).[8] However, by precisely controlling the power level, the scientists could balance reaction rates, which resulted in a 6-fold improvement in reaction time. In the future, the development of a photoreactor that can hold multiple reaction vials will enable accelerated discoveries for new technologies in fragment-based coupling reactions.
Figure 2

Balancing optimal output LED power for enhanced reactivity. Reprinted with permission from ref (7). Copyright 2017 American Chemical Society.

Balancing optimal output LED power for enhanced reactivity. Reprinted with permission from ref (7). Copyright 2017 American Chemical Society. Most importantly, these integrated photoreactors were implemented across 10 different medicinal chemistry groups at 4 different Merck research sites. This led to the successful standardization of LED protocols used across the sites. Synergistic partnerships between academia and industry often present opportunities to pool ideas and resources to solve synthetic challenges.[9] The advent of the integrated photoreactor should improve the ability to translate protocols from academia to industry due to its modularity and ease of use. This integrated photoreactor will augment the translation of protocols from academia to industry and light a path for developing the molecules of tomorrow.
  9 in total

1.  Ten key issues in modern flow chemistry.

Authors:  Jens Wegner; Sascha Ceylan; Andreas Kirschning
Journal:  Chem Commun (Camb)       Date:  2011-03-15       Impact factor: 6.222

2.  A photoflow reactor for the continuous photoredox-mediated synthesis of C-glycoamino acids and C-glycolipids.

Authors:  R Stephen Andrews; Jennifer J Becker; Michel R Gagné
Journal:  Angew Chem Int Ed Engl       Date:  2012-03-22       Impact factor: 15.336

Review 3.  Visible light photoredox catalysis with transition metal complexes: applications in organic synthesis.

Authors:  Christopher K Prier; Danica A Rankic; David W C MacMillan
Journal:  Chem Rev       Date:  2013-03-19       Impact factor: 60.622

4.  Visible-light photoredox catalysis in flow.

Authors:  Joseph W Tucker; Yuan Zhang; Timothy F Jamison; Corey R J Stephenson
Journal:  Angew Chem Int Ed Engl       Date:  2012-03-16       Impact factor: 15.336

5.  Discovery of an α-amino C-H arylation reaction using the strategy of accelerated serendipity.

Authors:  Andrew McNally; Christopher K Prier; David W C MacMillan
Journal:  Science       Date:  2011-11-25       Impact factor: 47.728

6.  Aryl amination using ligand-free Ni(II) salts and photoredox catalysis.

Authors:  Emily B Corcoran; Michael T Pirnot; Shishi Lin; Spencer D Dreher; Daniel A DiRocco; Ian W Davies; Stephen L Buchwald; David W C MacMillan
Journal:  Science       Date:  2016-06-23       Impact factor: 47.728

7.  Silyl Radical Activation of Alkyl Halides in Metallaphotoredox Catalysis: A Unique Pathway for Cross-Electrophile Coupling.

Authors:  Patricia Zhang; Chi Chip Le; David W C MacMillan
Journal:  J Am Chem Soc       Date:  2016-06-22       Impact factor: 15.419

8.  Academia-industry symbiosis in organic chemistry.

Authors:  Quentin Michaudel; Yoshihiro Ishihara; Phil S Baran
Journal:  Acc Chem Res       Date:  2015-02-23       Impact factor: 22.384

9.  A General Small-Scale Reactor To Enable Standardization and Acceleration of Photocatalytic Reactions.

Authors:  Chi Chip Le; Michael K Wismer; Zhi-Cai Shi; Rui Zhang; Donald V Conway; Guoqing Li; Petr Vachal; Ian W Davies; David W C MacMillan
Journal:  ACS Cent Sci       Date:  2017-05-17       Impact factor: 14.553

  9 in total

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