CCLX.—The labile nature of the halogen atom in organic compounds. Part V. The action of hydrazine on the halogen derivatives of some esters and substituted cyclohexanes
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/1922/CT/CT9222102169
Cited by 22 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. Conjugate halo- and mercuroazidation of 1-phenyltricyclo-[4.1.0.02.7]heptane. Synthesis of a conformationally rigid α-amino acid with a bicyclo[3.1.1]heptane skeleton;Russian Journal of Organic Chemistry;2016-07
2. Stereoselectivity of halomethoxylation of 1-phenyltricyclo-[4.1.0.02,7]heptane and methyl 7-phenyltricyclo[4.1.0.02,7]-heptane-1-carboxylate;Russian Journal of Organic Chemistry;2007-06
3. O- and N-Alkylation of N-halosuccinimides in ionic reactions with 1-phenyltricyclo [4.1.0.02,7]heptane;Russian Chemical Bulletin;2005-02
4. Stereochemistry of conjugate halogenation of 1-phenyltricyclo[4.1.0.02,7]heptane;Russian Journal of Organic Chemistry;2004-11
5. A Radical Version of the Bromo- and the Iodocyclization of Bis(homoallylic) Alcohols— The Synthesis of Halogenated Tetrahydrofurans by Stereoselective Alkoxyl Radical Ring Closures;European Journal of Organic Chemistry;2003-10
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