A self consistent field molecular orbital treatment of furan including all valence electrons
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference21 articles.
1. A self consistent field molecular orbital investigation of the importance of d orbital participation in the ground state of thiophene
2. D.T. Clark, submitted for publication.
3. Semiempirical SCF‐LCAO—MO Treatment of Furan
4. Structure �lectronique du furanne m�thode L.C.A. O. am�lior�e
5. The electronic structure of oxygen and sulfur heterocycles
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1. Physical Properties of Thiophene Derivatives;Chemistry of Heterocyclic Compounds: A Series Of Monographs;2008-01-02
2. Electron momentum spectroscopy study of furan;Chemical Physics;1998-02
3. Reactivity on Photooxidation of Selected Five-Membered Heterocyclic Flavor Compounds;Journal of Agricultural and Food Chemistry;1996-01-01
4. Stereospecific and Nucleophilic Additions of 2- and 3-Thienylmethylene. Reactions of 2- and 3-Thienylmethylene withcis- andtrans-Stilbene, Dimethyl Maleate, Dimethyl Fumarate, and Styrene Derivatives;Bulletin of the Chemical Society of Japan;1987-12
5. [2π+2σ] and [4π+2σ] Type Cycloaddition Reactions of Furan and Benzofurans with Benzocyclopropene;Bulletin of the Chemical Society of Japan;1987-11
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