PPT - Design and Development of Safe and Selective Deoxofluorinating Reagents PowerPoint Presentation - ID:6865556
![PDF] RECENT DEVELOPMENTS IN FLUORINATION CHEMISTRY OF DAST WITH SPECIAL REFERENCE TO ALCOHOLS | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/b4b752df74d43e44d3deebc422f07ece42518525/5-Figure5-1.png "PDF] RECENT DEVELOPMENTS IN FLUORINATION CHEMISTRY OF DAST WITH SPECIAL REFERENCE TO ALCOHOLS | Semantic Scholar")
PDF] RECENT DEVELOPMENTS IN FLUORINATION CHEMISTRY OF DAST WITH SPECIAL REFERENCE TO ALCOHOLS | Semantic Scholar
Synthesis of Cycloalkanoindoles by an Unusual DAST‐Triggered Rearrangement Reaction - Giannini - 2004 - European Journal of Organic Chemistry - Wiley Online Library
Diethylaminosulfur Trifluoride (DAST)
Rearrangement reactions in the fluorination of d-glucopyranoside at the C-4 position by DAST - ScienceDirect
Deoxyfluorination of alcohols with 3,3-difluoro-1,2-diarylcyclopropenes | Nature Communications
Fluorination with aminosulfuranes - Wikipedia
Deoxyfluorination of alcohols with 3,3-difluoro-1,2-diarylcyclopropenes | Nature Communications
Mechanism
Emerging fluorination methods in organic chemistry relevant for life science application - ScienceDirect
Gram-scale synthesis and transformations of products DAST... | Download Scientific Diagram
Fluorination with aminosulfuranes - Wikipedia
Deoxyfluorination of alcohols with 3,3-difluoro-1,2-diarylcyclopropenes | Nature Communications
Are carboxylic esters really refractory to DAST? On the fluorination of α-hydroxyesters with DAST - ScienceDirect
N,N-Dialkylaminosulfur Trifluoride Dethiofluorination | SpringerLink
Fluorination by sulfur tetrafluoride - Organic Reactions Wiki
Synthesis of Acyl Fluorides via DAST-Mediated Fluorinative C–C Bond Cleavage of Activated Ketones | Organic Letters
Fluorination with aminosulfuranes - Wikipedia
A modified fluoro-Pummerer reaction with DAST and NIS for synthesis of β-amino-α-fluoro-sulfides from corresponding β-amino-sulfides - ScienceDirect
Citations
Successive C-C bond cleavage, fluorination, trifluoromethylthio- and pentafluorophenylthiolation under metal-free conditions to provide compounds with dual fluoro-functionalization. - Abstract - Europe PMC
Fluorination by sulfur tetrafluoride - Organic Reactions Wiki
Successive C–C bond cleavage, fluorination, trifluoromethylthio- and pentafluorophenylthiolation under metal-free conditions to provide compounds with ... - Chemical Science (RSC Publishing) DOI:10.1039/C5SC04208A
