Stereoelectronic control in the solvolysis of spiroepoxidic 1-norbornyl triflates: unexpected reactivity in 3-bromomethyl derivatives-Reference-Cited by-同舟云学术

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Stereoelectronic control in the solvolysis of spiroepoxidic 1-norbornyl triflates: unexpected reactivity in 3-bromomethyl derivatives

Published:2011-04 Issue:15 Volume:52 Page:1762-1765
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Martínez Antonio García,Vilar Enrique Teso,Fraile Amelia García,Cerero Santiago de la Moya,Morillo Cristina Díaz

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference22 articles.

1. Strained Small Ring Compounds: Bridgehead Substituted Bicyclo [2.1.1]hexanes

2. Solvolysis of highly unreactive substrates using the trifluoromethanesulfonate (triflate) leaving group

3. Solvolytic reactivity of 4-tricyclyl, 1-apocamphyl, and 1-methyl-4-tricyclo[2.2.2.02,6]octyl trifluoromethanesulfonates. Observations on the interaction of the face of the cyclopropane ring with electrophiles and on the interpretation of activation parameters for solvolytic reactions

4. Cage Hydrocarbons;Müller,1991

5. Synthesis of substituted 1-norbornylamines with antiviral activity.

Cited by 2 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. Special ChiralC2-Symmetricendo-Biarylnorbornane: Synthesis and Structure Illustration;Chinese Journal of Chemistry;2014-07

2. Water-trapping of unstable carbocations taking place into the inverted region of the Marcus equation. First experimental and computational evidence;Tetrahedron;2012-04

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