A Remarkably Efficient Photochemical Methodology for Endo to Exo IsomerizatLon of Dials–Alder Cycloadducts
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/20/7/20_7_1173/_pdf
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4. ⊼-Facial Stereoselectivity in Diels-Alder Reaction of Hexacyclo [7.4.2.01,9.03,7.04,14.06,15] Pentadecane-10,12-diene-2,8-dione
5. Structure of hexacyclo[7.4.2.01,9.03,7.04,14.06,15]pentadeca-10,12-diene-2,8-dione
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1. Synthesis of (1r,2r,6s,7s)-4-Oxatricyclo[5.2.1.02,6]dec-8-ene-3,5-dione. Exo-5-norbornene-2,3-dicarboxyanhydride like a precursor for new optically active norbornene-type monomers;AIP Conference Proceedings;2022
2. Synthesis and characterization of hydrogenated poly(norbornene endo-dicarboximide)s prepared by ring opening metathesis polymerization;Polymer;2012-05
3. ChemInform Abstract: A Remarkably Efficient Photochemical Methodology for endo- to exo- Isomerization of Diels-Alder Cycloadducts.;ChemInform;2010-08-22
4. Stereoselective Transformations of meso Bicyclic Hydrazines: Versatile Access to Functionalized Aminocyclopentanes;Synthesis;2009-03-02
5. Preparation and structure of pyrrolo[2,1-b]- and isoindolo[1,2-b][3,1]epoxyquinazolines;Journal of Molecular Structure;2007-04
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