SulfoxFluor-enabled deoxyazidation of alcohols with NaN3

SulfoxFluor-enabled deoxyazidation of alcohols with NaN3

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Hypervalent silicate-assisted azidation approach for the substituted azepane motif - ScienceDirect

Publication - Organofluorine Chemistry Jinbo Hu Group

Deoxyfluorination with CuF2: Enabled by Using a Lewis Base Activating Group - Sood - 2020 - Angewandte Chemie International Edition - Wiley Online Library

Publications - Qin group

PDF) Organocatalytic Deoxyhalogenation of Alcohols with Inorganic Halides

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Modified and Scalable Synthesis of N-Tosyl-4-Chlorobenzenesulfonimidoyl Fluoride (SulfoxFluor): Direct Imidation of Sulfinyl Chlorides with Chloramine-T Trihydrate

SulfoxFluor as a deoxyfluorination reagent, and beyond - ScienceDirect

Rapid Deoxyfluorination of Alcohols with N‐Tosyl‐4‐chlorobenzenesulfonimidoyl Fluoride (SulfoxFluor) at Room Temperature - Guo - 2019 - Chemistry – A European Journal - Wiley Online Library

UV light promoted 'Metal'/'Additive'-free oxidation of alcohols: investigating the role of alcohols as electron donors - RSC Advances (RSC Publishing) DOI:10.1039/C9RA06490G

Corey-Kim Oxidation - Online Organic Chemistry Tutor

N-Chlorosuccinimide (NCS)–N,N-dimethylformamide (DMF), a reagent for the oxidation of benzylic alcohols to aldehydes and ketones

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论文发表- 有机氟化学重点实验室胡金波课题组