Regio- and stereoselectivity of additions of organometallics to - and -tricyclo[5.2.1.02,6]deca-4,8-dien-3-ones-Reference-Cited by-同舟云学术

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Regio- and stereoselectivity of additions of organometallics to - and -tricyclo[5.2.1.02,6]deca-4,8-dien-3-ones

Published:1993-01 Issue:48 Volume:49 Page:11353-11372
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Dols Paul P.M.A.,Verstappen Mariëlle M.H.,Klunder Antonius J.H.,Zwanenburg Binne

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference65 articles.

1. Bioassay-Abenteuer auf dem Weg zum Prostacyclin (Nobel-Vortrag)

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1. Facial Selectivity in the Addition of Lithium Dimethylcuprate to 6-Substituted Tricyclo[5.2.1.02,6]deca-4,8-dienones. Synthesis of β-Substituted Cyclopentenones Using Flash Vacuum Thermolysis;Australian Journal of Chemistry;2014

2. Determination of the absolute configurations using electronic and vibrational circular dichroism measurements and quantum chemical calculations;Tetrahedron: Asymmetry;2011-10

3. Retro-Diels-Alder Reactions of Masked Cyclopentadienones Catalyzed by Heterogeneous Brønsted Acids;Advanced Synthesis & Catalysis;2010-12-07

4. ChemInform Abstract: Regio- and Stereoselectivity of Additions of Organometallics to endoand exo-Tricyclo(5.2.1.02,6)deca-4,8-dien-3-ones.;ChemInform;2010-08-19

5. Facial selectivity in addition reactions to the highly strained enone in tricyclo[5.2.1.02,6]deca-2(6),8-dienone and tricyclo[5.2.1.02,6]dec-2(6)-enone;Tetrahedron;2009-03

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