The Vilsmeier formylation of N-(4-tolyl)pyrrolidine, -piperidine and -perhydroazepine: Further examples of the ‘t-amino effect’
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference5 articles.
1. Vilsmeier formylation of para-substituted tert-anilines results in dibenzo[1,5]diazocines or quinazolinium salts: a remarkable example of the ‘t-amino effect’
2. Heterocycles by Ring Closure of Ortho-Substituted t-Anilines (The t-Amino Effect)
3. “Tert-amino effect” in heterocyclic synthesis. Ring closure reactions of N,N-dialkyl-1,3-dien-1-amines
4. O. Meth-Cohn, Adv. Het. Chem., in press.
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1. Vilsmeier Formylation;Comprehensive Organic Name Reactions and Reagents;2010-09-15
2. Facile Formation of Cyclic Aminals through a Brønsted Acid-Promoted Redox Process;The Journal of Organic Chemistry;2008-11-21
3. Eight-membered Rings with Two Heteroatoms 1,5;Comprehensive Heterocyclic Chemistry III;2008
4. Surprising formylations with methylformamidopyridines and oxalyl chloride;Tetrahedron Letters;2000-04
5. Vilsmeier formylation of tert-anilines: dibenzo[b,f ][1,5]diazocines and quinazolinium salts via the ‘t-amino effect’1;Journal of the Chemical Society, Perkin Transactions 1;1998
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