Literature DB >> 29513400

The Molecular Industrial Revolution: Automated Synthesis of Small Molecules.

Melanie Trobe1, Martin D Burke1.   

Abstract

Today we are poised for a transition from the highly customized crafting of specific molecular targets by hand to the increasingly general and automated assembly of different types of molecules with the push of a button. Creating machines that are capable of making many different types of small molecules on demand, akin to that which has been achieved on the macroscale with 3D printers, is challenging. Yet important progress is being made toward this objective with two complementary approaches: 1) Automation of customized synthesis routes to different targets by machines that enable the use of many reactions and starting materials, and 2) automation of generalized platforms that make many different targets using common coupling chemistry and building blocks. Continued progress in these directions has the potential to shift the bottleneck in molecular innovation from synthesis to imagination, and thereby help drive a new industrial revolution on the molecular scale.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  artificial intelligence; flow chemistry; iterative synthesis; machine learning; small molecules

Mesh:

Substances:

Year:  2018        PMID: 29513400      PMCID: PMC5912692          DOI: 10.1002/anie.201710482

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  167 in total

1.  Development and application of a solution-phase automated synthesizer, 'ChemKonzert'.

Authors:  Kazuhiro Machida; Yoichiro Hirose; Shinichiro Fuse; Tohru Sugawara; Takashi Takahashi
Journal:  Chem Pharm Bull (Tokyo)       Date:  2010-01       Impact factor: 1.645

Review 2.  Automation synthesis modules review.

Authors:  S Boschi; F Lodi; C Malizia; G Cicoria; M Marengo
Journal:  Appl Radiat Isot       Date:  2012-09-26       Impact factor: 1.513

3.  Stereoretentive Suzuki-Miyaura coupling of haloallenes enables fully stereocontrolled access to (-)-peridinin.

Authors:  Eric M Woerly; Alan H Cherney; Erin K Davis; Martin D Burke
Journal:  J Am Chem Soc       Date:  2010-05-26       Impact factor: 15.419

4.  Titanium enolates of thiazolidinethione chiral auxiliaries: versatile tools for asymmetric aldol additions.

Authors:  M T Crimmins; K Chaudhary
Journal:  Org Lett       Date:  2000-03-23       Impact factor: 6.005

5.  (Z)-(2-bromovinyl)-MIDA boronate: a readily accessible and highly versatile building block for small molecule synthesis.

Authors:  Eric M Woerly; Justin R Struble; Nagarjuna Palyam; Sean P O'Hara; Martin D Burke
Journal:  Tetrahedron       Date:  2011-06-17       Impact factor: 2.457

6.  A simple and general platform for generating stereochemically complex polyene frameworks by iterative cross-coupling.

Authors:  Suk Joong Lee; Thomas M Anderson; Martin D Burke
Journal:  Angew Chem Int Ed Engl       Date:  2010-11-15       Impact factor: 15.336

7.  A machine-assisted flow synthesis of SR48692: a probe for the investigation of neurotensin receptor-1.

Authors:  Claudio Battilocchio; Benjamin J Deadman; Nikzad Nikbin; Matthew O Kitching; Ian R Baxendale; Steven V Ley
Journal:  Chemistry       Date:  2013-04-16       Impact factor: 5.236

Review 8.  Progress and prospects for small-molecule probes of bacterial imaging.

Authors:  Ozden Kocaoglu; Erin E Carlson
Journal:  Nat Chem Biol       Date:  2016-06-17       Impact factor: 15.040

Review 9.  Enabling Technologies for the Future of Chemical Synthesis.

Authors:  Daniel E Fitzpatrick; Claudio Battilocchio; Steven V Ley
Journal:  ACS Cent Sci       Date:  2016-02-24       Impact factor: 14.553

10.  A self optimizing synthetic organic reactor system using real-time in-line NMR spectroscopy.

Authors:  Victor Sans; Luzian Porwol; Vincenza Dragone; Leroy Cronin
Journal:  Chem Sci       Date:  2014-11-14       Impact factor: 9.825

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  18 in total

Review 1.  Automated Chemical Oligosaccharide Synthesis: Novel Approach to Traditional Challenges.

Authors:  Matteo Panza; Salvatore G Pistorio; Keith J Stine; Alexei V Demchenko
Journal:  Chem Rev       Date:  2018-06-28       Impact factor: 60.622

2.  Closing the Loop: Developing an Integrated Design, Make, and Test Platform for Discovery.

Authors:  David M Parry
Journal:  ACS Med Chem Lett       Date:  2019-05-15       Impact factor: 4.345

Review 3.  Expanding the medicinal chemistry synthetic toolbox.

Authors:  Jonas Boström; Dean G Brown; Robert J Young; György M Keserü
Journal:  Nat Rev Drug Discov       Date:  2018-08-24       Impact factor: 84.694

4.  Exploiting Chemical Toolboxes for the Expedited Generation of Tetracyclic Quinolines as a Novel Class of PXR Agonists.

Authors:  Bruno Cerra; Andrea Carotti; Daniela Passeri; Roccaldo Sardella; Giada Moroni; Alessandro Di Michele; Antonio Macchiarulo; Roberto Pellicciari; Antimo Gioiello
Journal:  ACS Med Chem Lett       Date:  2018-12-27       Impact factor: 4.345

5.  HPLC-Based Automated Synthesis of Glycans in Solution.

Authors:  Samira Escopy; Yashapal Singh; Keith J Stine; Alexei V Demchenko
Journal:  Chemistry       Date:  2022-05-25       Impact factor: 5.020

Review 6.  Synthesis and Glycosidation of Anomeric Halides: Evolution from Early Studies to Modern Methods of the 21st Century.

Authors:  Yashapal Singh; Scott A Geringer; Alexei V Demchenko
Journal:  Chem Rev       Date:  2022-06-08       Impact factor: 72.087

7.  Digitizing Chemical Synthesis in 3D Printed Reactionware.

Authors:  Andrius Bubliauskas; Daniel J Blair; Henry Powell-Davies; Philip J Kitson; Martin D Burke; Leroy Cronin
Journal:  Angew Chem Int Ed Engl       Date:  2022-03-25       Impact factor: 16.823

8.  Automated and Accelerated Synthesis of Indole Derivatives on a Nano-Scale.

Authors:  Shabnam Shaabani; Ruixue Xu; Maryam Ahmadianmoghaddam; Li Gao; Martin Stahorsky; Joe Olechno; Richard Ellson; Michael Kossenjans; Victoria Helan; Alexander Dömling
Journal:  Green Chem       Date:  2018-12-21       Impact factor: 10.182

9.  Peridinin Is an Exceptionally Potent and Membrane-Embedded Inhibitor of Bilayer Lipid Peroxidation.

Authors:  Hannah M S Haley; Adam G Hill; Alexander I Greenwood; Eric M Woerly; Chad M Rienstra; Martin D Burke
Journal:  J Am Chem Soc       Date:  2018-11-02       Impact factor: 15.419

10.  Controlling an organic synthesis robot with machine learning to search for new reactivity.

Authors:  Jarosław M Granda; Liva Donina; Vincenza Dragone; De-Liang Long; Leroy Cronin
Journal:  Nature       Date:  2018-07-18       Impact factor: 49.962

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