Synthesis of heterocyclic propellanes. Preparation and transannular reactions of 5-ethoxycarbonylmethylene-cyclooctanone and the corresponding oximes and hydrazones-Reference-Cited by-同舟云学术

Synthesis of heterocyclic propellanes. Preparation and transannular reactions of 5-ethoxycarbonylmethylene-cyclooctanone and the corresponding oximes and hydrazones

Published:1986-01 Issue:18 Volume:42 Page:5081-5088
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Malamidou-Xenikaki E.,Nicolaides D.N.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference19 articles.

1. X-Ray crystal structure analyses and conformational studies of cis-cyclo-octane-1,5-diol and cyclo-octane-1,5-dione

2. Medium Ring Compounds. XXIX. Cyclooctane-1,5-dione-dioxime

3. Carbon-13 N.M.R. shifts as a measure of transannular interaction in unsaturated alicyclic systems

4. Transannular addition to 1,5-dimethylenecyclo-octane

5. Photochemical Formation of [3,3,2]Propellanes from 1,5-Dimethylenecycloalkanes

Cited by 5 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. Photochemistry of Amines and Amino Compounds;PATAI'S Chemistry of Functional Groups;2009-12-15

2. Partially Saturated Polynuclear Isoxazoles;Chemistry of Heterocyclic Compounds: A Series Of Monographs;2008-01-02

3. Stereoselective synthesis of some novel heterocyclic estrone derivatives by intramolecular 1,3-dipolar cycloaddition;Tetrahedron;2002-08

4. Transannular cyclization reactions of cyclooctane-1,5-dione and 5-ethoxycarbonylmethylenecyclooctanone upon treatment with diamines. An efficient one-pot synthesis of substituted 2,6-diazatricyclo[5.3.3.01,6]- and 2,5-diazatricyclo[4.3.3.01,5]-alkanes and a study of their acetylation products;Journal of the Chemical Society, Perkin Transactions 1;1996

5. ChemInform Abstract: Synthesis of Heterocyclic Propellanes. Preparation and Transannular Reactions of 5-Ethoxycarbonylmethylene-cyclooctanone and the Corresponding Oximes and Hydrazones.;ChemInform;1987-01-27