DOI: 10.1055/b-00000091

Methoden der Organischen Chemie (Houben-Weyl)

DOI: 10.1055/b-003-111710 Online ISBN 9783131939715
de Meijere, Armin: 1997

Carbocyclic Three- and Four-Membered Ring Compounds

Print ISBN 9783131077745 · Online ISBN 9783131968845
Volume: E 17 f
Weitere Informationen

Buch

Herausgeber: de Meijere, Armin

Autoren: Butenschön, H.; Chan, T.-L.; de Meijere, A.; Haber, S.; Haufe, G.; Imming, P.; Kozhushkov, S. I.; Mann, G.; Margaretha, P.; Muchall, H. M.; Regitz, M.; Seitz, G.; Shing, T. K. M.; Sydnes, L. K.

Titel: Carbocyclic Three- and Four-Membered Ring Compounds

Print ISBN: 9783131077745; Online ISBN: 9783131968845; Buch-DOI: 10.1055/b-003-111710

4th Edition © 1997 Georg Thieme Verlag KG
Georg Thieme Verlag KG, Stuttgart

Fachgebiete: Organische Chemie

Houben-Weyl (Chemistry)



Übergeordnete Publikation

Titel: Methoden der Organischen Chemie (Houben-Weyl)

Print ISBN: 9783131400840; Online ISBN: 9783131939715; DOI: 10.1055/b-00000091

Typ: Mehrbändiges Werk

Einführung
8. Cyclobutenes: A. Synthesis: 1. By Construction of the System
1.1. From a C4 Building Block
1.2. From a C3 and a C1 Building Block
1.3. From Two C2 Building Blocks
8. Cyclobutenes: A. Synthesis: 2. By Rearrangement of the Carbon Framework
2.1. Homopropargyl Rearrangement
2.2. Rearrangement with Hydrogen Transfer
2.3. Valence Isomerizations (I)
2.3. Valence Isomerizations (II)
8. Cyclobutenes: A. Synthesis: 3. By Ring Enlargement
3.1. Via Cyclopropylcarbenes
3.2. From Cyclopropylmethanols, Cycloprop-2-enylmethanols and Their Derivatives
3.3. From Bi(cyclopropenyl)s
3.4. Via Cyclopropylvinyl Cations
3.5. From Cyclopropenes and Metal Carbonyl Compounds
8. Cyclobutenes: A. Synthesis: 4. By Ring Contraction
4.1. From Five-Membered Rings
4.2. From Six -Membered Rings
8. Cyclobutenes: A. Synthesis: 5. By Transformation of Other Cyclobutenes
5.1. With Cleavage of a Cyclobutenyl to Carbon Bond
5.2. Without Cleavage of a Cyclobutenyl to Carbon Bond (I)
5.2. Without Cleavage of a Cyclobutenyl to Carbon Bond (II)
5.2. Without Cleavage of a Cyclobutenyl to Carbon Bond (III)
8. Cyclobutenes: B. Transformations: 1. With Retention of the Ring
1. With Retention of the Ring T. K. M. SHING
8. Cyclobutenes: B. Transformations: 2. Ring-Opening Reactions
2.1. Addition Reactions
2.2. Cycloaddition Reactions
2.3. Cycloreversion Reactions
2.4. Rearrangement Reactions (I)
2.4. Rearrangement Reactions (II)
2.4. Rearrangement Reactions (III)
8. Cyclobutenes: C. Coordination Chemistry
1. Cyclobutenes
2. Benzocyclobutene and Related Systems
9. Cyclobutenediones: A. Synthesis
1. Alkyl, Alkenyl, Alkynyl and Aryl Derivatives of Cyclobutenedione
2. Benzocyclobutenediones
3. Thio- and Seleno-Substituted Cyclobutenediones
9. Cyclobutenediones: B. Transformations
1. Alkyl-, Alkenyl-, Alkynyl- and Aryl-Substituted Cyclobutenediones
2. Benzocyclobutenediones
3. Thio- and Seleno-Substituted Cyclobutenediones
9. Cyclobutenediones: C. Coordination Chemistry
C. Coordination Chemistry
10. Cyclobutadienes: A. Synthesis
1. Cycloreversions
2. Ring Expansions by Cyclopropenylcarbene to Cyclobutadiene Isomerizations
3. Dimerization of Alkynes
4. Liberation of Cyclobutadiene Ligands by Cleavage of Cyclobutadiene–Metal Complexes
5. Tetrahedrane to Cyclobutadiene Valence Isomerizations
10. Cyclobutadienes: B. Transformations
1. Oxidation of Cyclobutadienes
2. [4 + 1] Cycloadditions Using Cyclobutadienes as Dienes
3. [3 + 2] Cycloadditions Using Cyclobutadienes as Dipolarophiles
4. [4 + 2] Cycloadditions
Anhang