On the dichotomy of the SN2/ET reaction pathways: an apparent SN2 reactivity in the reaction of naphthalene dianion with alkyl fluorides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. Electron transfer, naphthalene radical anion, and alkyl halides
2. Production and reduction of alkyl radicals under controlled, homogenous conditions through reactions of alkyl flourides with sodium naphthalenide. Rate constant for cyclization of 5-hexenyl radicals.
3. Reactions of primary alkyl fluorides with sodium naphthalene and related compounds
4. On the Mechanism of Arene-Catalyzed Lithiation: The Role of Arene Dianions—Naphthalene Radical Anion versus Naphthalene Dianion
5. On the mechanism of the naphthalene-catalysed lithiation: the role of the naphthalene dianion
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3. On the reactivity of naphthalene and biphenyl dianions: tying up loose ends concerning an SN 2-ET dichotomy in alkylation reactions;Journal of Physical Organic Chemistry;2015-03-02
4. Reductive Removal of the Pivaloyl Protecting Group from Tetrazoles by a Naphthalene-Catalyzed Lithiation Process;Synthesis;2014-11-27
5. Detritylation of Protected Tetrazoles by Naphthalene-Catalyzed Lithiation;Synthesis;2014-04-30
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