Acid‐Induced Stereoselective Formation of 3,5‐Cycloheptadien‐1‐ones from Ketenes and Dienes
Author:
Affiliation:
1. Institut für Organische Chemie und Biochemie der Universität Freiburg, Albertstraße 21, D‐79104 Freiburg, Germany
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19941270715
Reference41 articles.
1. Zur Kenntniss der Ketene. Diphenylketen
2. Ketene, XXXII.: Cyclobutan‐Derivate aus Diphenyl‐keten und Äthylen‐Verbindungen
3. Theoretical study of (2 + 2) cycloadditions. Ketene with ethylene
4. Do supra-antara paths really exist for 2 + 2 cycloaddition reactions? Analytical computation of the MC-SCF Hessians for transition states of ethylene with ethylene, singlet oxygen, and ketene
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1. ChemInform Abstract: Acid-Induced Stereoselective Formation of 3,5-Cycloheptadien-1-ones from Ketenes and Dienes.;ChemInform;2010-08-18
2. Asymmetric Michael addition and deracemization of enolate by chiral crown ether;Tetrahedron;1998-01
3. Unusual reactions between chloroketenes and 1,3,5-tri-tert-butylcyclopentadiene;Liebigs Annalen;1995-11
4. Asymmetric Michael reaction. Deracemization of enolate by chiral crown ether;Tetrahedron Letters;1995-08
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