Barton–Zard reaction - Wikipedia
CAS#:29166-72-1 | 2-tert-butyl-1,1,3,3-tetramethylguanidine | Chemsrc
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Anhydrous tertiary alkanolamines as hybrid chemical and physical CO 2 capture reagents with pressure-swing regeneration - Energy & Environmental Science (RSC Publishing) DOI:10.1039/C0EE00506A
Lewis Base-Boryl Radical Enabled Giese Reaction and Barton Decarboxylation of N-Hydroxyphthalimide (NHPI) Esters
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Kinetics screening of the N -alkylation of organic superbases using a continuous flow microfluidic device: basicity versus nucleophilicity - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C2OB25215E
Organic liquid CO2 capture agents with high gravimetric CO2 capacity
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Rapid Synthesis of Chiral 1,2‐Bisphosphine Derivatives through Copper(I)‐Catalyzed Asymmetric Conjugate Hydrophosphination - Yue - 2020 - Angewandte Chemie International Edition - Wiley Online Library
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Barton–Zard reaction - Wikipedia
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Proposed catalytic cycle and TS of the present vinylogous addition of... | Download Scientific Diagram
Copper(I)‐Catalyzed Asymmetric Vinylogous Aldol‐Type Reaction of Allylazaarenes - Wang - 2021 - Angewandte Chemie International Edition - Wiley Online Library
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Construction of Chiral 2,3‐Allenols through a Copper(I)‐Catalyzed Asymmetric Direct Alkynylogous Aldol Reaction - Zhong - 2020 - Angewandte Chemie International Edition - Wiley Online Library
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Synthesis of Highly Oxygenated Dinaphthyl Ethers via SNAr Reactions Promoted by Barton's Base | Organic Letters
Synthesis of Highly Oxygenated Dinaphthyl Ethers via SNAr Reactions Promoted by Barton's Base | Organic Letters
2-tert-Butyl-1,1,3,3-tetramethylguanidine - Wikipedia
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