Classical conformational analysis of strained organic molecules. I. [l,m,n]Propellanes withl,m,n equal to 2, 3, and 4
Author:
Publisher
Wiley
Subject
Computational Mathematics,General Chemistry
Reference16 articles.
1. [1.1.1]Propellane
2. Structure of [4.4.4]propellane and [4.4.4]propellatriene byX-ray Analysis
3. Inverted tetrahedral geometry at a bridgehead carbon. X-ray crystal, molecular, and electronic structure of 8,8-dichlorotricyclo[3.2.1.01.5]octane (C8H10Cl2) at -40.deg.
4. The Crystal and Molecular Structure of Tetracyclo[6.4.3.0.02,7]pentadec-4-en-13-one
5. Structures of the [n.2.2]propellanes. I
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1. Propellane as a conformational device for the stabilization of the β-lactone of salinosporamide A;Tetrahedron;2009-08
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3. π-Relaxation of the ring strain: design of polycyclic unsaturated silicon molecules;Tetrahedron;2006-05
4. Non-empirical calculations of NMR indirect carbon–carbon coupling constants. Part 6: Propellanes;Magnetic Resonance in Chemistry;2003-12-19
5. Electrophilic and Oxidative Activation of the Central C−C Bond in [3.3.n]Propellanes: A Theoretical Study;The Journal of Organic Chemistry;1998-08-26
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