The stereochemistry of the adducts derived from the Diels-Alder addition of cyclobutenes and cyclopentadienones: A caveat on some existing PMR methods for the assignment of stereochemistry
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference4 articles.
1. Cyclobutyl edge participation in the thermal elimination of carbon monoxide from polyalicyclic ketones
2. SN2' reactions of cis-3,4-dichlorocyclobutene
3. Synthesis and nuclear magnetic resonance spectra of some bridged polyhydromethanonaphthalenes. Bridge proton assignments
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1. The preparation of rigidly-linked 4,5-diazafluorenes: New molrac bidentate ligand systems;Tetrahedron Letters;1996-03
2. v-Triazolines. part XXIII;Tetrahedron;1986-01
3. Aromatic solvent induced shifts (ASIS) in 1H N.M.R. spectra; A graphical analysis;Tetrahedron;1982-01
4. Reactions of cyclo-octatetraene and its derivatives - X;Tetrahedron;1981-01
5. ChemInform Abstract: THE STEREOCHEMISTRY OF THE ADDUCTS DERIVED FROM THE DIELS-ALDER ADDITION OF CYCLOBUTENES AND CYCLOPENTADIENONES: A CAVEAT ON SOME EXISTING PMR METHODS FOR THE ASSIGNMENT OF STEREOCHEMISTRY;Chemischer Informationsdienst;1979-11-20
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