Methoden der Organischen Chemie (Houben-Weyl)
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Einzeltitel
Synthesis pf Peptides and Peptidomimetics, Author, Keyword and Preparation Index
Houben-Weyl Methods of Organic Chemistry Vol. E 22c, 4th Edition Supplement
Houben-Weyl Methods of Organic Chemistry Vol. E 22a, 4th Edition Supplement
Houben-Weyl Methods of Organic Chemistry Vol. E 22b, 4th Edition Supplement
Synthesis of Peptides and Peptidomimetics
Substance index
Substance index
Substance index
Synopsis of the Structure I
Substance Index Cyclic Compounds VIII, Polycyclic Compounds I
Houben-Weyl Methods of Organic Chemistry Vol. E 23d/1, 4th Edition Supplement
Indexes to the Complete E-Series
Substance index: from the 4th edition and the additional and supplementary volumes to the 4th edition
Substance Index
Substance Index
Organo-Fluorine Compounds / Methods Index
Substance Index
Organo-Fluorine Compounds
Substance Index Cyclic Compounds VIII, Tricyclic compounds II
Substance index : from the 4th edition and the additional and supplementary volumes to the 4th edition
Organo-fluorine compounds
Substance Index
Organo-Fluorine Compounds
Substance Index
Substance Index
Substance index
Index of Experimental Procedures of Classes of Substances and individual Compounds (CH…Index)
Index of Experimental Procedures of Classes of Substances and Individual Compounds (Ch…Index)
Hetarenes IV
Hetarenes IV
Hetarenes IV
Organo-Fluorine Compounds
Hetarenes IV
Carbocyclic Three- and Four Membered Ring Compounds
Hetarenes IV
Carbocyclic Three- and Four-Membered Ring Compounds
Carbocyclic Three- and Four-Membered Ring Compounds
Carbocyclic Three- and Four Membered Ring Compounds
Carbocyclic Three- and Four-Membered Ring Compounds
Hetarenes IV
Carbocyclic Three- and Four Membered Ring Compounds
Stereoselective Synthesis
Stereoselective Synthesis
Stereoselective Synthesis
Stereoselective Synthesis
Stereoselective Synthesis
Stereoselective Synthesis
Hetarene III
Hetarene III
Hetarene I
Hetarene I
Hetarene III
Hetarene I
Ene-X and Yne-X Compounds
Ene-X and Yne-X Compounds
En,X- und In,X-Verbindungen
Hetarene III
Carbanionen
Hal/O(S,N)-, S/S(N)-, N/N-Acetale : Hal/O-, O/O-Acetale als anomere Zentren von Kohlenhydraten
Hetarene II
Organische Stickstoffverbindungen III
Organische Stickstoffverbindungen IV
Hetarene
Organische Stickstoff-Verbindungen 1 Teil 2/2
0/0- und 0/S-Acetale
Erweiterungs- und Folgeband
Organotellurium Compounds
Carbokationen, Carbokationen-Radikale
Organische Stickstoff-Verbindungen mit einer C,N-Doppelbindung
Organische Stickstoff-Verbindungen 1 Teil 1/2
Carbene (Carbenoide)
C-Radikale
Organische Peroxo-Verbindungen
Register der Stoffklassen
Register der Stoffklassen
Makromolekulare Stoffe
Sachregister zu Band E 4, Autorenregister zu den Bänden E 4, E 5, E 11
Metallorganische Verbindungen
Organo-л-Verbindungen als Hilfsmittel in der organischen Chemie
Register der Arbeitsvorschriften von Stoffklassen (alphabetisch) und Einzelverbindungen
Organische Schwefel-Verbindungen
Carbonsäuren und Carbonsäure-Derivate
Carbocyclische π-Elektronen-Systeme
Metallorganische Verbindungen
Alkohole
Organobor-Verbindungen III
Organoboron Compounds II
Aldehyde
Kohlensäure-Derivate
Organobor-Verbindungen
Organische Phosphor-Verbindungen I
Organische Phosphor-Verbindungen II
Oxidation
Reduktion
Arene und Arine
Organo-Silicium-Verbindungen
Alkohole
Reduktion
Alkohole
Chinone, Teil 2
Chinone
Enole, endiole (reduktone) Biosynthesen von Hydroxy-Verbindungen
Metallorganische Verbindungen
Metallorganische Verbindungen: Germanium, Zinn
Alkine, Di- und Polyine, Allene, Kumulen
Chinone
Ketone
Ketone
Phenole
Metallorganische Verbindungen
Photochemie
Oxidation II
Photochemie
Synthese von Peptiden
Metallorganische Verbindungen Hg
Synthese von Peptiden
Metallorganische Verbindungen
Ketone
Offenkettige und cyclische Polyene, En-ine
Alkene, Cycloalkene, Arylalkene
Stickstoffverbindungen 1
Carbocyclische Dreiring-Verbindungen
Isocyclische Vierring-Verbindungen
Metallorganische Verbindungen: Li, Na, K, Rb, Cs, Cu, Ag, Au
Kohlenwasserstoffe
Metallorganische Verbindungen: Al, Ga, In, Tl
Kohlenwasserstoffe
Sauerstoffverbindungen 2
Stickstoffverbindungen 1
Stickstoffverbindungen 1
Sauerstoffverbindungen I
Sauerstoffverbindungen I
Stickstoffverbindungen 1
Organische Phosphor-Verbindungen
Sauerstoffverbindungen I
Makromolekulare Stoffe
Organische Phosphor-Verbindungen
Makromolekulare Stoffe
Halogenverbindungen. Fluorverbindungen. Chlorverbindungen
Halogenverbindungen
Allgemeine Laboratoriumspraxis
Allgemeine Laboratoriumspraxis
Stickstoffverbindungen 2
Stickstoffverbindungen 1
Physikalische Methoden
Schwefel-, Selen-, Tellur-Verbindungen
Allgemeine chemische Methoden
Physikalische Methoden
Sauerstoffverbindungen 2
Analytische Methoden
Sauerstoffverbindungen 3
Stickstoffhaltige Gruppen
Die Methoden der Organischen Chemie
Die Methoden der Organischen Chemie
Die Methoden der Organischen Chemie
Stickstoffhaltige Gruppen und Organometallverbindungen
Die Methoden der Organischen Chemie
Methoden der Organischen Chemie
Analytische Methoden
Analytische Methoden
Analytische Methoden
Aktuell angezeigt
Meijere, Armin de: 1997
Carbocyclic Three- and Four-Membered Ring Compounds
Print ISBN 9783132187047; Online ISBN 9783131968340
Weitere Informationen
Buch
Herausgeber: Meijere, Armin de
Autoren: Baird, M.S.; Bertrand, G.; De Kimpe, N.; Fedorynski, M.; Friese, C.; Heydt, H.; Jendralla, H.; Jonczyk, A.; Klunder, A.J.H.; Maas, G.; Margaretha, P.; Mayer, D.; Munschauer, R.; Schmidt, Th.; Stolle, A.; Subramanian, L. R.; Sydnes, L.K.; Wiberg, K.; Zeller, K.-P.; Zwanenburg, B.
Titel: Carbocyclic Three- and Four-Membered Ring Compounds
Alternativer Titel:
Print ISBN 9783132187047; Online ISBN 9783131968340; Buch-DOI 10.1055/b-003-113721
Copyright Verlagsgruppe Georg Thieme, Stuttgart, New York, Delhi, Rio
Fachgebiete: Organische Chemie
Houben-Weyl (Chemistry)
Buchreihen
Methoden der Organischen Chemie (Houben-Weyl)
Print ISBN 9783131400840; Online ISBN 9783131939715; DOI 10.1055/b-00000091
Typ: Mehrbändiges Werk
Einführung
Synthesis Introduction
Introduction
1. Cyclopropanes: A. Synthesis: 1. By Construction of the System: 1.1. From a C
3
Building Block
1.1.1. 1,3-Elimination of Two Heteroatoms
1.1.2. 1,3-Coupling
1.1.3. 1,3-Elimination of HX, Where X is a Heteroatom or Heteroatom-Containing Function and (I)
1.1.3. 1,3-Elimination of HX, Where X is a Heteroatom or Heteroatom-Containing Function and (II)
1.1.3. 1,3-Elimination of HX, Where X is a Heteroatom or Heteroatom-Containing Function and (III)
1.1.4. By Photochemically Induced Ring Closure via Intramolecular Hydrogen Abstraction
1.1.5. By Intramolecular ?-C-H Insertion of a Carbene
1.1.6. From Cyclopropenes (I)
1.1.6. From Cyclopropenes (II)
1.1.6. From Cyclopropenes (III)
1.1.6. From Cyclopropenes (IV)
1.1.6. From Cyclopropenes (V)
1.1.6. From Cyclopropenes (VI)
1.1.6. From Cyclopropenes (VII)
Cyclopropanes: A. Synthesis: 2. By Rearrangement of the Carbon 1.2. From a C2 and a C1 Building Block
1.2.1. By Reaction of the C-C Double Bond (I)
1.2.1. By Reaction of the C-C Double Bond (II)
1.2.1. By Reaction of the C-C Double Bond (III)
1.2.1. By Reaction of the C-C Double Bond (IV)
1.2.1. By Reaction of the C-C Double Bond (V)
1.2.1. By Reaction of the C-C Double Bond (VI)
1.2.1. By Reaction of the C-C Double Bond (VII)
1.2.1. By Reaction of the C-C Double Bond (VIII)
1.2.1. By Reaction of the C-C Double Bond (IX)
1.2.1. By Reaction of the C-C Double Bond (X)
1.2.1. By Reaction of the C-C Double Bond (XI)
1.2.1. By Reaction of the C-C Double Bond (XII)
1.2.1. By Reaction of the C-C Double Bond (XIII)
1.2.1. By Reaction of the C-C Double Bond (XIV)
1.2.1. By Reaction of the C-C Double Bond (XV)
1.2.1. By Reaction of the C-C Double Bond (XVI)
1.2.1. By Reaction of the C-C Double Bond (XVII)
1.2.1. By Reaction of the C-C Double Bond (XVIII)
1.2.1. By Reaction of the C-C Double Bond (XIX)
1.2.1. By Reaction of the C-C Double Bond (XX)
1.2.1. By Reaction of the C-C Double Bond (XXI)
1.2.1. By Reaction of the C-C Double Bond (XXII)
1.2.1. By Reaction of the C-C Double Bond (XXIII)
1.2.1. By Reaction of the C-C Double Bond (XXIV)
1.2.1. By Reaction of the C-C Double Bond (XXV)
1.2.1. By Reaction of the C-C Double Bond (XXVI)
1.2.1. By Reaction of the C-C Double Bond (XXVII)
1.2.1. By Reaction of the C-C Double Bond (XXVIII)
1.2.2. Reaction of Oxiranes with Carbanions
Cyclopropanes: A. Synthesis: 2. By Rearrangement of the Carbon 2.1. Homoallyl and Cyclobutyl to Cyclopropylmethyl Rearrangements
2.1.1. Rearrangement of Homoallylic Compounds
Cyclopropanes: A. Synthesis: 2. By Rearrangement of the Carbon 2.2. Light-Induced Rearrangements
2.2.1. From
α,β
-Unsaturated Cyclic Carbonyl Compounds
2.2.2. Rearrangements via Cyclopropane Intermediates
2.2.2. Rearrangements via Cyclopropane Intermediates
Cyclopropanes: A. Synthesis: 2. By Rearrangement of the Carbon 2.3. Electrocyclic Reactions
2.3.1. Allyl to Cyclopropyl Rearrangement
2.3.1. Allyl to Cyclopropyl Rearrangement
2.3.1. Allyl to Cyclopropyl Rearrangement
2.3.2. Thermally or Photochemically Induced Sigmatropic and Electrocyclic Rearrangements
Anhang
Auflagen
Auflage
1997 - 1. Edition
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