#flow synthesis

[amcrasto]

Utilization of fluoroform for difluoromethylation in continuous flow: a concise synthesis of α-difluoromethyl-amino acids

Utilization of fluoroform for difluoromethylation in continuous flow: a concise synthesis of [small alpha]-difluoromethyl-amino acids Green Chem., 2018, 20,108-112 DOI: 10.1039/C7GC02913F, Communication  Open Access   This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.Manuel Kockinger, Tanja Ciaglia, Michael Bersier, Paul Hanselmann, Bernhard Gutmann, C. Oliver…

View On WordPress

[amcrasto]

Photochemical intramolecular amination for the synthesis of heterocycles

Photochemical intramolecular amination for the synthesis of heterocycles

  Green Chem., 2017, Advance Article DOI: 10.1039/C7GC02261A, Communication Shawn Parisien-Collette, Corentin Cruche, Xavier Abel-Snape, Shawn K. Collins Polycyclic heterocycles can be formed in good to excellent yields via photochemical conversion of the corresponding substituted aryl azides under irradiation with purple LEDs in a continuous flow reactor. Photochemical intramolecular amination…

View On WordPress

[amcrasto]

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

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

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

Green Chem., 2017, 19,3006-3013 DOI: 10.1039/C7GC00657H, Paper Nelly Ntumba Tshibalonza, Jean-Christophe M. Monbaliu Highly selective flash deoxydehydration of glycerol towards allyl alcohol under continuous-flow conditions. From the journal:Green Chemistry Revisiting the deoxydehydration of…

View On WordPress

[amcrasto]

Continuous Microflow Synthesis of Fuel Precursors from Platform Molecules Catalyzed by 1,5,7-Triazabicyclo[4.4.0]dec-5-ene

    The first continuous flow synthesis of C8–C16 alkane fuel precursors from biobased platform molecules is reported. TBD (1,5,7-triazabicyclo[4.4.0]dec-5-ene) was found to be a recyclable and highly efficient organic base catalyst for the aldol condensation of furfural with carbonyl compounds, and the selectivity of mono- or difuryl product can be easily regulated by adjusting the molar ratio…

View On WordPress

[amcrasto]

Development of a concise, scalable synthesis of a CCR1 antagonist utilizing a continuous flow Curtius rearrangement

Development of a concise, scalable synthesis of a CCR1 antagonist utilizing a continuous flow Curtius rearrangement

Development of a concise, scalable synthesis of a CCR1 antagonist utilizing a continuous flow Curtius rearrangement Green Chem., 2017, Advance Article DOI: 10.1039/C6GC03123D, Paper Maurice A. Marsini, Frederic G. Buono, Jon C. Lorenz, Bing-Shiou Yang, Jonathan T. Reeves, Kanwar Sidhu, Max Sarvestani, Zhulin Tan, Yongda Zhang, Ning Li, Heewon Lee, Jason Brazzillo, Laurence J. Nummy, J. C. Chung,…

View On WordPress

[amcrasto]

Highly Selective Phosgene-Free Carbamoylation of Aniline by Dimethyl Carbonate under Continuous-Flow Conditions

Highly Selective Phosgene-Free Carbamoylation of Aniline by Dimethyl Carbonate under Continuous-Flow Conditions

Over the last 20 years organic carbamates have found numerous applications in pesticides, fungicides, herbicides, dyes, pharmaceuticals, cosmetics, and as protecting groups and intermediates for polyurethane synthesis. Recently, in order to avoid phosgene-based synthesis of carbamates, many environmentally benign and alternative pathways have been investigated. However, few examples of…

View On WordPress

[amcrasto]

Continuous-Flow Diazotization

    Continuous-Flow Diazotization for Efficient Synthesis of Methyl 2-(Chlorosulfonyl)benzoate: An Example of Inhibiting Parallel Side Reactions Zhiqun Yu†, Hei Dong†, Xiaoxuan Xie†, Jiming Liu‡, and Weike Su*†‡ † National Engineering Research Center for Process Development of Active Pharmaceutical Ingredients, Collaborative Innovation Center of Yangtze River Delta Region Green…

View On WordPress

[amcrasto]

Heck–Matsuda Reaction in Flow

Heck–Matsuda Reaction in Flow

Product 3 was obtained as a mixture of diastereomers (58:42). The NMR data are consistent with literature precedent.20a

Major diastereomer: 1H NMR (300 MHz, CDCl3) δ (ppm) 7.25-7.28 (m, 2H), 7.14-7.17 (m, 2H), 5.14 (dd, 1H, J = 2.5, 5.8 Hz), 4.29 (t, 1H, J = 8.3 Hz), 3.79 (dd, 1H, J = 6.9, 8.4 Hz), 3.54-3.62 (m, 1H), 3.38 (s, 3H), 2.32 (dd, 1H, J = 7.7, 12.9 Hz), 2.04 (ddd, 1H, J = 5.1, 9.3,…

View On WordPress