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Towards the generalized iterative synthesis of small molecules

Nature reviews. Chemistry, 2018-02, Vol.2 (2), Article 0115

2018

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Enantioselective installation of adjacent tertiary benzylic stereocentres using lithiation-borylation-protodeboronation methodology. Application to the synthesis of bifluranol and fluorohexestrol

Chemical science (Cambridge), 2015-07, Vol.6 (7), p.3718-3723

2015

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Synthesis of Enantioenriched Tertiary Boronic Esters by the Lithiation/Borylation of Secondary Alkyl Benzoates

Journal of the American Chemical Society, 2013-10, Vol.135 (43), p.16054-16057

2013

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Axial shielding of Pd(II) complexes enables perfect stereoretention in Suzuki-Miyaura cross-coupling of Csp3 boronic acids

Nature communications, 2019-03, Vol.10 (1), p.1263-1263, Article 1263

2019

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Modular synthesis enables molecular ju-jitsu in the fight against antibiotic resistance

Nature (London), 2020-10, Vol.586 (7827), p.32-33

2020

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Digitizing Chemical Synthesis in 3D Printed Reactionware

Angewandte Chemie International Edition, 2022-06, Vol.61 (24), p.e202116108-n/a

International ed. in English, 2022

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Modular synthesis enables molecular ju-jitsu

Nature (London), 2020-10, Vol.586 (7827), p.32-33

2020

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A Mild Method for Making MIDA Boronates

Organic letters, 2020-12, Vol.22 (24), p.9408-9414

2020

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Selective uni- and bidirectional homologation of diborylmethane

Chemical science (Cambridge), 2017-04, Vol.8 (4), p.2898-2903

2017

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Erratum: Towards the generalized iterative synthesis of small molecules

Nature reviews. Chemistry, 2018-03, Vol.2 (3), Article 0128

2018

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Stereocontrolled Synthesis of Adjacent Acyclic Quaternary-Tertiary Motifs: Application to a Concise Total Synthesis of (−)-Filiformin

Angewandte Chemie International Edition, 2014-05, Vol.53 (22), p.5552-5555

International ed. in English, 2014

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Automated iterative Csp3–C bond formation

Nature (London), 2022-04, Vol.604 (7904), p.92-97

2022

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Preparation of MIDA Anhydride and Reaction with Boronic Acids

Organic syntheses, 2022, Vol.99, p.92-112

Chen, Peng-Jui

2022

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Stereospecific conversion of alcohols into pinacol boronic esters using lithiation-borylation methodology with pinacolborane

Chemical communications (Cambridge, England), 2014-04, Vol.50 (31), p.4053-4055

2014

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Digitizing Chemical Synthesis in 3D Printed Reactionware

Angewandte Chemie, 2022-06, Vol.134 (24), p.n/a

2022

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The total synthesis of (−)-aplysin via a lithiation–borylation–propenylation sequence

Tetrahedron, 2012-09, Vol.68 (37), p.7598-7604

2012

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Stereocontrolled Synthesis of Adjacent Acyclic Quaternary-Tertiary Motifs: Application to a Concise Total Synthesis of (−)-Filiformin

Angewandte Chemie, 2014-05, Vol.126 (22), p.5658-5661

2014

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A Computer Conquers Tactical Combinations

Chem, 2020-01, Vol.6 (1), p.12-13

2020

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A practical solution to the numerical butterfly effect in chaotic systems for fast but memory limited computers

2010 42nd Southeastern Symposium on System Theory (SSST), 2010, p.335-339

2010

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Rapid automated iterative small-molecule synthesis

Nature Synthesis, 2024-08, Vol.3 (8), p.1031-1038

2024

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Publisher Correction: Rapid automated iterative small-molecule synthesis

Nature Synthesis, 2024-06, Vol.3 (8), p.1061-1061

2024

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Enantioselective installation of adjacent tertiary benzylic stereocentres using lithiation-borylation-protodeboronation methodology. Application to the synthesis of bifluranol and fluorohexestrolElectronic supplementary information (ESI) available: Detailed experimental procedures and spectroscopic data for all new compounds. X-Ray data analysis for compound 2. See DOI: 10.1039/c4sc03901g

2015-06

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Enantioselective installation of adjacent tertiary benzylic stereocentres using lithiation–borylation–protodeboronation methodology. Application to the synthesis of bifluranol and fluorohexestrol† †Electronic supplementary information (ESI) available: Detailed experimental procedures and spectroscopic data for all new compounds. X-Ray data analysis for compound 2. See DOI: 10.1039/c4sc03901g

Chemical science (Cambridge), 2015-04, Vol.6 (7), p.3718-3723

2015

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Selective uni- and bidirectional homologation of diborylmethaneElectronic supplementary information (ESI) available: General procedures, synthetic details and NMR spectra. See DOI: 10.1039/c6sc05338f

2017-03

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Selective uni- and bidirectional homologation of diborylmethane† †Electronic supplementary information (ESI) available: General procedures, synthetic details and NMR spectra. See DOI: 10.1039/c6sc05338f Click here for additional data file

Chemical science (Cambridge), 2017-02, Vol.8 (4), p.2898-2903

2017

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Towards the generalized iterative synthesis of small molecules

Enantioselective installation of adjacent tertiary benzylic stereocentres using lithiation-borylation-protodeboronation methodology. Application to the synthesis of bifluranol and fluorohexestrol

Synthesis of Enantioenriched Tertiary Boronic Esters by the Lithiation/Borylation of Secondary Alkyl Benzoates

Axial shielding of Pd(II) complexes enables perfect stereoretention in Suzuki-Miyaura cross-coupling of Csp3 boronic acids

Modular synthesis enables molecular ju-jitsu in the fight against antibiotic resistance

Digitizing Chemical Synthesis in 3D Printed Reactionware

Modular synthesis enables molecular ju-jitsu

A Mild Method for Making MIDA Boronates

Selective uni- and bidirectional homologation of diborylmethane

Erratum: Towards the generalized iterative synthesis of small molecules

Stereocontrolled Synthesis of Adjacent Acyclic Quaternary-Tertiary Motifs: Application to a Concise Total Synthesis of (−)-Filiformin

Automated iterative Csp3–C bond formation

Preparation of MIDA Anhydride and Reaction with Boronic Acids

Stereospecific conversion of alcohols into pinacol boronic esters using lithiation-borylation methodology with pinacolborane

Digitizing Chemical Synthesis in 3D Printed Reactionware

The total synthesis of (−)-aplysin via a lithiation–borylation–propenylation sequence

Stereocontrolled Synthesis of Adjacent Acyclic Quaternary-Tertiary Motifs: Application to a Concise Total Synthesis of (−)-Filiformin

A Computer Conquers Tactical Combinations

A practical solution to the numerical butterfly effect in chaotic systems for fast but memory limited computers

Rapid automated iterative small-molecule synthesis

Publisher Correction: Rapid automated iterative small-molecule synthesis

Selective uni- and bidirectional homologation of diborylmethaneElectronic supplementary information (ESI) available: General procedures, synthetic details and NMR spectra. See DOI: 10.1039/c6sc05338f

Selective uni- and bidirectional homologation of diborylmethane† †Electronic supplementary information (ESI) available: General procedures, synthetic details and NMR spectra. See DOI: 10.1039/c6sc05338f Click here for additional data file

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