Publications of 2021

[2021][447x359] Flow neutralization of sulfur-containing

Flow neutralization of sulfur-containing chemical warfare agents with Oxone: packed-bed vs. aqueous solution

A. Delaune, S. Mansour, B. Picard, P. Carrasqueira, I. Chataigner, L. Jean, P.-Y. Renard, J.-C. M. Monbaliu and Julien Legros*

Green Chem. 2021, 23, 2925-2930

DOI: 10.1039/D1GC00449B

[2021][447x238]A Modular_2

A Modular, Low Footprint and Scalable Flow Platform for the Expedient α-Aminohydroxylation of Enolizable Ketones

V.-E. Kassin, R. Morodo, T. Toupy, I. Jacquemin, K. Van Hecke, R. Robiette and J.-C. M. Monbaliu*

Green Chem. 2021, 23, 2336-2351

DOI: 10.1039/D0GC04395H 

Inside Front cover : March 2021 issue 21

Highlighted in : OPRD (Some items of Interest to Process R&D Chemists and Engineers)

Publications of 2020

[2020][447x225]] Au Nanobipyr

Au Nanobipyramids@mSiO2 Core-Shell Nanoparticles for Plasmon-Enhanced Singlet Oxygen Photooxygenations in Segmented Flow Microreactors

C. Mendoza, A. Désert, D. Chateau, C. Monnereau, L. Khrouz, F. Lerouge, C. Andraud, J.-C. M. Monbaliu, S. Parola and B. Heinrichs

Nanoscale Adv. 2020, 2, 5280-5287

DOI: 10.1039/D0NA00533A

[2020][447x447] Continuous Flow Upgrading

Continuous Flow Upgrading of Selected C2-C6 Platform Chemicals Derived from Biomass

R. Gérardy, D. P. Debecker, J. Estager, P. Luis and J.-C. M. Monbaliu*

Chem. Rev. 2020, 120, 15, 7219-7347

DOI: 10.1021/acs.chemrev.9b00846

[2020][447x451] Continuous Flow Organophosphorus

Continuous flow organophosphorus chemistry

R. Morodo, P. Bianchi and J.-C. M. Monbaliu*

Eur. J. Org. Chem. 2020, 33, 5236-5277

DOI: 10.1002/ejoc.202000430

Front cover : September 2020 issue 33

Tagged as Very Important Paper

Featured in the special Collection YourJOC Talents 2020

A safe and compact flow platform for the neutralization of a mustard gas simulant with air and light

A safe and compact flow platform for the neutralization of a mustard gas simulant with air and light

N. Emmanuel, P. Bianchi, J. Legros and J.-C. M. Monbaliu*

Green Chem. 2020, 22, 4105-4115

DOI: 10.1039/D0GC01142H

Outside back cover : July 2020 issue 13

Scalable and robust photochemical flow process towards small spherical gold nanoparticles

Scalable and robust photochemical flow process towards small spherical gold nanoparticles

P. Bianchi, G. Petit and J.-C. M. Monbaliu*

React. Chem. Eng. 2020, 5, 1224-1236

DOI: 10.1039/D0RE00092B

Inside back cover : July 2020 issue 7

The deoxydehydration (DODH) reaction: a versatile technology for accessing olefins from bio-based polyols

The deoxydehydration (DODH) reaction: a versatile technology for accessing olefins from bio-based polyols

N. Ntumba Tshibalonza and J.-C. M. Monbaliu*

Green Chem. 2020, 22, 4801-4848

DOI: 10.1039/D0GC00689K

Outside front cover : August 2020 issue 15

[2020][447x339] Separation of bio_based

Separation of bio-based chemicals using pervaporation

W. Li, J. Estager, J.-C. M. Monbaliu, D. Debecker and P. Luis

J. Chem. Technol. Biotechnol. 2020, 95, 2311–2334

DOI: 10.1002/jctb.6434

[2020] Radical C-H F-Difluoromethylation of [447x285]

Radiosynthesis of [18F]difluoromethyl heteroaryl-sulfones for radical C-H 18F-difluoromethylation of heteroarenes by visible light photoredox catalysis

A Lemos, L. Trump, B. Lallemand, P. Pasau, J. Mercier, C. Lemaire, J.-C. M. Monbaliu, C. Genicot and A. Luxen

Catalysts 2020, 10, 275

DOI: 10.3390/catal10030275

[2019] Metal-free hydroxylation [447x168]

Metal-free hydroxylation of tertiary ketones under intensified and scalable continuous flow conditions

V.-E. H. Kassin, T. Toupy, G. Petit, P. Bianchi, E. Salvadeo  and J.-C. M. Monbaliu*

J. Flow Chem. 2020, 10, 167-179

DOI: 10.1007/S41981-019-00073-6

[2020] Supported ionic liquid membranes for the separation [447x310]

Supported ionic liquid membranes for the separation of methanol/dimethyl carbonate mixtures by pervaporation

W. Li, C. Molina Fernandez, J. Estager, J.-C. M. Monbaliu, D. Debecker and P. Luis

J. Membr. Sci. 2020, 598, 117790

DOI: 10.1016/j.memsci.2019.+117790

[2019] Allentoine3 [447x216]

Development of a sustainable continuous flow approach toward allantoin

E. Salvadeo and J.-C. M. Monbaliu

J. Flow Chem. 2020, 10, 251-257

DOI: 10.1007/S41981-019-00056-7

Publications of 2019

[2019] Versatile and scalable synthesis of cyclic organic carbonates [447x193]

Versatile and scalable synthesis of cyclic organic carbonates under organocatalytic continuous flow conditions

R. Gérardy, J. Estager, P. Luis, D. P. Debecker and J.-C. M. Monbaliu*

Catal. Sci. Technol. 2019, 9, 6841-6851

DOI: 10.1039/C9CY01659G

Outside Front Cover : December 2019 issue 24

[2019] Understanding chemical interaction [447x223]

Understanding chemical interaction between phosphonate-derivative molecules and silver surface cluster in SERS: a combined experimental and computational approach

G. Emonds-Alt, B. Mignolet, C. Malherbe, J.-C. M. Monbaliu, F. Remacle and G. Eppe*

Phys. Chem. Chem. Phys. 2019, 21, 22180-22187

DOI: 10.1039/C9CP01615E

[2019] Continuous flow upgrading of glycerol toward [447x122]

Continuous flow upgrading of glycerol toward oxiranes and active pharmaceutical ingredients thereof

R. Morodo, R. Gérardy, G. Petit and J.-C. M. Monbaliu*

Green Chem. 2019, 21, 4422-4433

DOI: 10.1039/C9GC01819K

[2019] Expedient Preparation of Active Pharmaceutical Ingredient Ketamine under Sustainable Continuous Flow Conditions

Expedient Preparation of Active Pharmaceutical Ingredient Ketamine under Sustainable Continuous Flow Conditions

V.-E. Kassin, R. Gérardy, T. Toupy, D. Collin, E. Salvadeo, F. Toussaint, K. Van Hecke and J.-C. M. Monbaliu*

Green Chem. 2019, 21, 2952-2966

DOI: 10.1039/C9GC00336C

Part of the themed collection : 2019 Green Chemistry Hot Articles

Inside Front Cover : June 2019 issue 11

[2019] Native chemical ligation and extended methodologies

Native chemical ligation and extended methodologies. Mecanisms, catalysis, scope and limitations

V. Agouridas, O. El Mahdi, V. Diemer, M. Cargoët, J.-C. M. Monbaliu* and O. Melnyk*

Chem. Rev. 2019, 112, 7328-7443

DOI: 10.1021/acs.chemrev.8b00712

[2019] Solubility Determination and Correlation of Warfarin [447x234]

Solubility Determination and Correlation of Warfarin Sodium 2-Propanol Solvate in Pure, Binary, and Ternary Solvent Mixture

M. V. George De la Rosa, R. Santiago, J. Malavé Romero, J. Duconge, J.-C. M. Monbaliu, V. López-Mejías, T. Stelzer

J. Chem. Eng. Data 2019, 64, 1399–1413

DOI: 10.1021/acs.jced.8b00977

[2019] Finding the perfect match [447x150]

Finding the perfect match: a combined computational and experimental study towards efficient and scalable photosensitized [2+2]cycloadditions in flow

J. Williams, M. Nakano, R. Gérardy, J. A. Rincon, O. de Frutos, C. Mateos, J.-C. M. Monbaliu and C. O. Kappe

Org. Process Res. Dev. 2019, 23, 78-87

DOI: 10.1021/acs.oprd.8b00375

[2018] Solvent-free organocatalytic [447x269]

Solvent-free organocatalytic preparation of cyclic organic carbonates under scalable continuous flow conditions

Z. Wang, R. Gérardy, G. Gauron, C. Damblon and J.-C. M. Monbaliu*

React. Chem. Eng. 2019, 4, 17-26

DOI: 10.1039/c8re00209f

[2018] sustaining the transition[447x269]

Sustaining the transition from petro-  to biobased chemical industry with flow chemistry

R. Gérardy, R. Morodo, J. Estager, P. Luis, D. P. Debecker, and J.-C. M. Monbaliu*

Top. Curr. Chem. 2019, 377:1

DOI: 10.1007/s41061-018-0222-3

Publications of 2018

[2018] Production of 3-butene-1,2-diol and vinyl ethylene carbonate from erythritol [447x269]

A versatile biobased continuous flow strategy for the production of 3-butene-1,2-diol and vinyl ethylene carbonate from erythritol

N. Ntumba Tshibalonza, R.Gérardy, Z. Alsafra, G. Eppe and J.-C. M. Monbaliu*

Green Chem. 2018, 20, 5147-5157

DOI: 10.1039/C8GC02468E

Part of the themed collection : 2018 Green Chemistry Hot Articles

[2018] Improving Continuous Flow Singlet [447x269]

Improving Continuous Flow Singlet Oxygen Photooxygenations with Functionalized Mesoporous Silica Nanoparticles

C. Mendoza, N. Emmanuel, C. A. Páez, L. Dreesen*, J.-C. M. Monbaliu* and B. Heinrich*

ChemPhotoChem 2018, 2, 890-897

DOI: 10.1002/cptc.201800148

Part of the special issue : Flow photochemistry

[2018] Application of pervaporation [447x269]

Application of pervaporation in the bio-production of glycerol carbonate

W. Li, R. Sreerangappa, J. Estager, J.-C. M. Monbaliu, D. P. Debecker, P. Luis

Chem. Eng. Process. 2018, 132, 127-136

DOI: 10.1016/j.cep.2018.08.014

[2018] Sorption and pervaporation study [447x269]

Sorption and pervaporation study of methanol/diméthyl carbonate mixture with poly(etheretherketone) (PEEK-WC) membrane

W. Li,F. Galiano, J. Estager, J.-C. M. Monbaliu, D. P. Debecker, A. Figoli, P. Luis

J. Memb. Sci. 2018, 567, 303-310

DOI: 10.1016/j.memsci.2018.09.040

[2018] Accelerated microfluidic [447x269]

Accelerated microfluidic native chemical ligation at difficult amino acids toward cyclic peptides

N. Ollivier, T. Toupy, R. C. Hartkoorn, R. Desmet, J.-C. M. Monbaliu* and O. Melnyk*

Nat. Commun. 2018, 9, 2847

DOI: 10.1038/s41467-018-05264-8

Highlighted in : SYNFACTS of the month

Featured in : 2018 Synthetic and Medicinal Chemistry issue of Nature Communication

[V1] Cover Feature [500x500]

“Continuous Flow Organic Chemistry: Successes and Pitfalls at the Interface with Current Societal Challenges”

R. Gérardy, N. Emmanuel, T. Toupy, V. Kassin, N. Ntumba Tshibalonza, M. Schmitz, J.-C. M. Monbaliu*

Eur. J. Org. Chem. 2018, 2301-2351

DOI:10.1002/ejoc.201800149

Tagged as Very Important Paper

Most Accessed paper in June 2018

Featured in the special Collection EurJOC Readers’ Choice 2019

NODAGA-PRGD2_abstract2018-3

“NOTA–PRGD2 and NODAGA–PRGD2: Bioconjugation, Characterization, Radiolabelling & Design Space”

M. Salvé, H. T. Avohou, J.-C. M. Monbaliu, P. Lebrun, C. Lemaire, C. Damblon, P. de Tullio, R. Hustinx and A. Luxen

J. Label. Cmpd. Radiopharm. 2018, 61, 487-500

DOI:10.1002/jlcr.3613

1-s2.0-S101060301731362X-sc1

“Transitioning from macroscopic batch to microfluidic processes for the efficient singlet oxygen photooxygenation of methionine”

C. Mendoza, N. Emmanuel, C. Paez, L. Dreesen*, J.-C. M. Monbaliu* and B. Heinrichs*

J. Photochem. Photobiol. 2018, 356,193-200

DOI:10.1016/j.jphotochem.2017.12.028)

Publications of 2017

Continuous-flow preparation of g-butyrolactone scaffolds from renewable fumaric and itaconic acids under photosensitized conditions

“Continuous-flow preparation of g-butyrolactone scaffolds from renewable fumaric and itaconic acids under photosensitized conditions”

R. Gérardy, M. Winter, C. R. Horn., A. Vizza, K. Van Hecke and J.-C. M. Monbaliu*

Org. Process Res. Dev. 2017, 21, 2012–2017

DOI:10.1021/acs.oprd.7b00314

op-2017-002127_0003

“Scalable Photocatalytic Oxidation of Methionine under Continuous-Flow Conditions”

N. Emmanuel, C. Mendoza, M. Winter, C. Horn, A. Vizza, L. Dreesen, B. Heinrichs and J.-C. M. Monbaliu*

Org. Process Res. Dev. 2017, 21, 1435-1438

DOI:10.1021/acs.oprd.7b00212

Get2

“Revisiting the deoxydehydration of glycerol towards allyl alcohol under continuous-flow conditions”

N. Ntumba Tshibalonza and J.-C. M. Monbaliu*

Green Chem. 2017, 19, 3006-3013

DOI:10.1039/C7GC00657H

ed-2016-00899u_0001

“Exploring the Fundamentals of Microreactor Technology with Multidisciplinary Lab Experiments Combining the Synthesis and the Characterization of Inorganic Nanoparticles”

N. Emmanuel, G. Emonds-Alt, M. Lismont*, G. Eppe* and J.-C. M. Monbaliu*

J. Chem. Edu. 2017, 94, 775–780

DOI:10.1021/acs.jchemed.6b00899

Get

“Assessing inter- and intramolecular continuous-flow strategies towards methylphenidate (Ritalin) hydrochloride”

R. Gérardy, M. Winter, A. Vizza and J.-C. M. Monbaliu*

React. Chem. Eng. 2017, 2, 149-158

DOI:10.1039/C6RE00184J

Featured in : the themed collection Reaction Chemistry & Engineering Emerging Investigators

2016

  • “Expanding chemistry’s horizon with continuous-flow reactors” J.-C. M. Monbaliu*, N. Emmanuel and R. Gérardy, Chimie Nouvelle 2016, 122, 18-26 (here)
  • “Compact and integrated approach for advanced end-to-end production, purification, and aqueous formulation of lidocaine hydrochloride”, J.-C. M. Monbaliu, T. Stelzer, E. Revalor, N. Weeranoppanant, K. F. Jensen, A. S. Myerson, Org. Process Res. Dev. 2016, 20, 1347-1353 (doi: 10.1021/acs.oprd.6b00165)
  • “Continuous-flow N-heterocyclic carbenes generation and organocatalysis”, L. Di Marco, M. Hans, L. Delaude and J.-C. M. Monbaliu*, Chem. Eur. J. 2016, 22, 4508–4514 (doi: 10.1002/chem.201505135)
    Tagged as hot paper and highlighted on Chemistry Views (here)
  • “Accelerating chemoselective peptide bond formation using bis(2-selenylethyl)amido peptide selenoester surrogates”, L. Raibaut, M. Cargoët, N. Ollivier, Y.-M. Chang, H. Drobecq, E. Boll, R. Desmet, J.-C. M. Monbaliu* and Oleg Melnyk*, Chem. Sci. 2016, 7, 2657-2665 (doi: 10.1039/C5SC03459K)

2015

  • “Continuous-flow thermolysis for the preparation of vinylglycine derivatives”, N. Lamborelle, J. Simon, A. Luxen and J.-C. M. Monbaliu*, Org. Biomol. Chem. 2015, 13, 11602-11606 (doi: 10.1039/C5OB02036K)
  • “Preparation, reactivity and synthetic utility of simple benzotriazole derivatives”, R. Gérardy and J.-C. M. Monbaliu*, Top. Heterocycl. Chem. 2015, 1-66 (doi: 110.1007/7081_2015_179)
  • “Efficient continuous flow benzotriazole activation and coupling of amino acids”, S. Seghers, F. E. A. Van Waes, A. Cukalovic, J.-C. M. Monbaliu et al., J. Flow Chem., 2015, 5, 220-227 (doi: 10.1556/1846.2015.00029)

2014

  • “New benzotriazole-based reagents for the phosphonylation of various N-, O- and S-nucleophiles”, Pandmand, A. D. Tiwari, S. Panda, J.-C. M. Monbaliu et al., Tetrahedron Lett. 2014, 55, 5898-5901 (doi: 10.1016/j.tetlet.2014.07.057)
  • “L’intensification des procédés chimiques, une approche radicale”, C. Henneuse, J.-C. M. Monbaliu, Athena 2014, 18-21 (here)
  • “Feruloyl benzotriazole and Weinreb amide as bioinspired building blocks: a reactivity study towards O-, N-, S- and C-nucleophiles”, B. I. Roman, J.-C. M. Monbaliu et al., Eur. J. Org. Chem. 2014, 2594-2611. (doi: 10.1002/ejoc.201301895)

2013

  • “Capture of benzotriazole-based Mannich electrophiles by CH-acidic compounds”, J.-C. M. Monbaliu, L. K. Beagle et al., RSC Advances 2013, 3, 4152-4155 (doi: 10.1039/C3RA22826F)
  • “Governing parameters of long-range intramolecular S-to-N acyl transfers within chemical ligation of peptides”, J.-C. M. Monbaliu, G. Dive et al., J. Chem. Theory Comp. 2013, 927-934 (doi: 10.1021/ct300830k)
  • “Development, optimization and scale-up of biodiesel production from crude palm oil and effective use in developing countries”, A. Cukalovic, J.-C. M. Monbaliu et al., Biomass & Bioenerg. 2013, 56, 62-69 (doi: 10.1016/j.biombioe.2013.04.015)

2012

  • “Recent trends in Cys- and Ser/Thr-based chemical ligations for the elaboration of peptide constructs”, J.-C. M. Monbaliu and A. R. Katritzky, Chem. Commun. 2012, 48, 11601-11622 (doi: 10.1039/C2CC34434C)
  • “A convenient synthesis of difficult medium-sized cyclic peptides by Staudinger-mediated ring closure”, K. Ha, J.-C. M. Monbaliu et al., Org. Biomol. Chem. 2012, 10, 8055-8058 (doi: 10.1039/C2OB25996F)
  • “En route towards ?-benzotriazoyl nitroso derivatives”, J.-C. M. Monbaliu, Lucas Beagle et al., RSC Advances 2012, 2, 8941-8945 (doi: 10.1039/C2RA21311G)
  • “Efficient synthesis of 2,5-diketopiperazines by Staudinger-mediated cyclization”, L. Beagle, F. Hansen, J.-C. M. Monbaliu et al., Synlett 2012, 23, 2337-2340 (doi: 10.1055/s-0031-1290446)
  • “User-friendly and flexible Kiliani-Fisher reaction on ketoses using microreaction technology”, J.-C. M. Monbaliu, A. Cukalovic et al., J. Flow Chem. 2012, 2, 43-46 (doi: 10.1556/JFC-D-12-00003)
  • “Long-range intramolecular S-N acyl migration: a study of the formation of native peptide analogs via 13-, 15- and 16-membered cyclic transition states”, K. Ha, M. Chahar, J.-C. M. Monbaliu et al., J. Org. Chem. 2012, 77, 2637-2648 (doi: 10.1021/jo2023125)
  • “A new benzotriazole-mediated stereoflexible gateway to hetero-2,5-diketopiperazines”, J.-C. M. Monbaliu, F. K. Hansen et al., Chem. Eur. J. 2012, 18, 2632-2638 (doi: 10.1002/chem.201103143)

2011

  • “Continuous-flow production of alkyl nitrites”, J.-C. M. Monbaliu*, J. Jorda et al., Chemistry Today 2011, 29, 80-82 (here)
  • “Electron-deficient 1- and 2-aza-1,3-dienes: a comprehensive survey of their synthesis and reactivity
    J.-C. M. Monbaliu, K. G. R. Masschelein and C. V. Stevens, Chem. Soc. Rev. 2011, 40, 4708-4739 (doi: 10.1039/C1CS15070G)
  • “Effective production of the biodiesel additive STBE by a continuous flow process”, J.-C. M. Monbaliu, M. Winter et al., Bioresour. Technol. 2011, 102, 9304-9307 (doi: 10.1016/j.biortech.2011.07.007)

2010

  • “Straightforward hetero Diels-Alder cycloadditions of nitroso dienophiles by microreactor technology”,J.-C. M. Monbaliu, A. Cukalovic et al., Tetrahedron Lett. 2010, 51, 5830-5833 (doi: 10.1016/j.tetlet.2010.08.117)
  • “Feasibility study for industrial production of fuel additives from glycerol”,
    J.-C. M. Monbaliu, M. Winter et al., Chemistry Today 2010, 28, 42-45 (here)
  • “[4+2] Cycloaddition of 1-phosphono-1,3-butadienes with nitroso-heterodienophiles: a new and versatile entry to polyfunctionalized ?– and ?-aminophosphonic derivatives”, J.-C. M. Monbaliu, B. Tinant et al, J. Org. Chem. 2010, 75, 5478-5486 (doi: 10.1021/jo100230r)
  • “HD-A cycloadditions of 1-diethoxyphosphoryl-1,3-butadiene with nitroso- and azo-heterodienophiles: a theoretical investigation”, J.-C. M. Monbaliu*, G. Dive et al., J. Mol. Struct.: THEOCHEM. 2010, 959, 49-54 (doi: 10.1016/j.theochem.2010.08.004)
  • “Three unrelated sphingomyelin analogs spontaneously cluster into plasma membrane micrometric domains”, D. Tyteca, L. D’Auria, P. Van Der Smissen, T. Medts, S. Carpentier, J.-C. M. Monbaliu et al., BBA-Biomembrane 2010, 1978, 909-927 (doi: 10.1016/j.bbamem.2010.01.021)
  • “Novel chiral 1-phosphono-1,3-butadiene for asymmetric hetero Diels-Alder cycloadditions with nitroso and azodicarboxylate dienophiles”, J.-C. M. Monbaliu, D. Peeters et al., Tetrahedron Lett. 2010, 51, 1052-1055 (doi: 10.1016/j.tetlet.2009.12.063)

2009

  • “Is anthracene cofactor or spectator for the thermolysis of anthracenyl acylnitroso cycloadducts in the presence of a diene?”, J.-C. M. Monbaliu*, J. Marchand-Brynaert et al., Tetrahedron Lett. 2009, 50, 2555-2558 (doi: 10.1016/j.tetlet.2009.03.062)
  • “A practical synthesis of 3-diethoxyphosphoryl-1,2-pyridazine derivatives”, J.-C. M. Monbaliu, J. Marchand-Brynaert, Synthesis 2009, 11, 1876-1880 (doi: 10.1055/s-0028-1088056)
  • (R)-4-phenyloxazolidin-2-thione: an efficient chiral auxiliary for [4+2] cycloaddition of 1-aminodienes and activated phosphonodienophiles, J.-C. M. Monbaliu, R. Robiette et al, Tetrahedron Lett. 2009, 50, 1314-1317 (doi: 10.1016/j.tetlet.2009.01.036)

2008

  • “Reactivity of (R)-4-phenyloxazolidin-2-thione chiral auxiliary: from deprotection to heterocyclic interconversion”, J.-C. M. Monbaliu, B. Tinant et al., Heterocycles 2008, 75, 2459-2475 (doi: 10.3987/COM-08-11410)
  • “[4+2] Cycloaddition of 1-phosphono-1,3-butadiene with azo- and nitroso-heterodienophiles”, J.-C. M. Monbaliu and J. Marchand-Brynaert, Tetrahedron Lett. 2008, 49, 1839-1842 (doi: 10.1016/j.tetlet.2008.01.050)
  • “NMR and X-ray diffraction analysis of 3-thioamido-5-phosphono-1-cyclohexene derivatives: Conformational and stereochemical assignments”, J.-C. M. Monbaliu, B. Tinant et al, J. Mol. Struct. 2008, 879, 113-118 (doi: 10.1016/j.molstruc.2007.08.018)

Books and Book Chapters

  • Multistep continuous-flow processes for the preparation of heterocyclic active pharmaceutical ingredients, Topics in Heterocyclic Chemistry: Flow Chemistry for the Synthesis of Heterocycles (Editor: E. V. Van der Eycken), Springer, 2018, in Press
    R. Gérardy and J.-C. M. Monbaliu
  • The chemistry of benzotriazole derivatives: a tribute to Alan Roy Katritzky, Topics in Heterocyclic Chemistry (Editor: J.-C. M. Monbaliu), Springer, 2015
  • Safety Aspects related to Microreactor Technology, in Flow Chemistry (Editors: Darvas, F.; Dormán, G.; Hessel, V.), Vol. 2, 247-276, De Gruyter, Berlin, 2014
    J.-C. M. Monbaliu, A. Cukalovic and C. V. Stevens
  • Microreactor technology as an efficient tool for multicomponent reactions, in Topics in Heterocyclic Chemistry: Synthesis of Heterocycles via Multicomponent Reactions, (Editors: R. V. A. Orru and E. Ruijter), Vol. 23, 161-198, Springer, 2010.
    A. Cukalovic, J.-C. M. Monbaliu and C. V. Stevens
  • Hetero Diels-Alder (HDA) reactions of 1-phosphono-1,3-butadienes with azo and nitroso dienophiles: an entry towards versatile heterocyclic synthons for aminophosphonic compounds in Targets in Heterocyclic Systems, (Editors: O. A. Attanasi, and D. Spinelli), Vol. 14, 49-79, Springer: Berlin, 2010.
    J.-C. M. Monbaliu, E. Villemin, B. Elias and J. Marchand-Brynaert

Patents

  • J.-C. M. Monbaliu, D. Collin, V.-E. Kassin “Improvements in or relating to organic material” Patent application No. EP17211200.5
  • J.-C. M. Monbaliu, N. N Tshibalonza “Process for the production of allyl compounds by deoxydehydration of glycerol” Patent application No. EP17159230
  • J.-C. M. Monbaliu, M. Hans “Continuous flow process for the polymerization of an alkylene oxide” WO 2018/114416 – EP3339350 (link to Espacenet).
  • J.-C. M. Monbaliu, R. Gérardy “Method for the preparation of alkyl phenidates”, WO 2018/050546 – EP73296292 (link to Espacenet).
  • K. F. Jensen, T. F. Jamison, A. Myerson, J.-C. M. Monbaliu, et al. “Systems and Methods for Synthesizing Chemical Products, Including Active Pharmaceutical Ingredients”, WO 2016/025803 (link to Espacenet).