Ring contraction of a two-carbon bridged spiropentane
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. Structures and energies of the tricyclo[4.1.0.01,3]heptanes and the tetracyclo[4.2.1.02,905,9]nonanes. Extended group equivalents for converting ab initio energies to heats of formation
2. Tricyclo[2.1.0.01,3]pentane
3. Bridged spiropentanes: Ring expansion
4. Organic Synthesis with .alpha.-Diazo Carbonyl Compounds
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1. Modern Organic Synthesis with α-Diazocarbonyl Compounds;Chemical Reviews;2015-08-18
2. Imines and Their N-Substituted Derivatives: Hydrazones and Other N,N-Derivatives Including Diazo Compounds;Comprehensive Organic Functional Group Transformations II;2005
3. Hemispiroalkaplanes: Hydrocarbon Cage Systems with a Pyramidal-Tetracoordinate Carbon Atom and Remarkable Basicity;Chemistry - A European Journal;2000-07-03
4. Synthesis and Reactivity of trans-Tricyclo[4.2.0.01,3]oct-4-ene;The Journal of Organic Chemistry;2000-05-11
5. The Chemistry of Highly Strained Oligospirocyclopropane Systems;Chemical Reviews;1999-12-09
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