N-Benzyltriflamide: A generally useful mitsunobu reagent for amine synthesis
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
1. Retro-Cope eliminations in the synthesis of 1,2,5-oxadiazinanes from allylamines and nitrones: a method for the amination of unactivated alkenes
2. Synthesis of Primary Allylic Amines
3. Improved Synthesis of ChiralN-Protected Allylic Amines
4. Allylamine Functionalization through .beta.-Nitrogen-Functionalized Organolithium Compounds
5. Silver iodide mediated amination reaction of allylic chlorides with lithium bis(trimethylsilyl)amide: a new synthetic method of N,N-disilylallylamines via lithium amide argentates
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4. Reactions of triflate esters and triflamides with an organic neutral super-electron-donor;Organic & Biomolecular Chemistry;2012
5. ChemInform Abstract: N-Benzyltriflamide: A Generally Useful Mitsunobu Reagent for Amine Synthesis.;ChemInform;2010-08-12
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