S→N type Smiles rearrangement of the aminoethanethiol moiety attached to heterocyclic compounds-Reference-Cited by-同舟云学术

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S→N type Smiles rearrangement of the aminoethanethiol moiety attached to heterocyclic compounds

Published:2010-05 Issue:19 Volume:66 Page:3452-3456
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Mountford Simon J.,Campi Eva M.,Robinson Andrea J.,Hearn Milton T.W.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference26 articles.

1. Pyridine Chemistry. I. The Smiles Rearrangement of the 3-Amino-2,2'-dipyridyl Sulfide System1

2. Aromatic Nucleophilic Substitution Reactions.

3. Rearrangement of 2-Aryloxybenzazoles

4. Sulfur-containing Pyridine Derivatives. LVI. Smiles Rearrangement of Pyridine Derivatives and Synthesis of Benzopyrido-and Dipyrido-1, 4-thiazine Derivatives. (4).

5. Dichotomy on intramolecular aromatic substitution caused by the smiles rearrangement

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Intramolecular SNAr Reactions;Modern Nucleophilic Aromatic Substitution;2013-06-03

2. Molecular Rearrangements: Part 2. Other Reactions;Organic Reaction Mechanisms Series;2012-12-04

3. Nucleophilic Aromatic Substitution;Organic Reaction Mechanisms Series;2012-12-04

4. Six-Membered Ring Systems;Progress in Heterocyclic Chemistry;2011

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