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Carbanion Chemistry / Robert B. Bates, Craig A. Ogle.

By: Contributor(s): Material type: TextTextPublisher: Berlin ; Boston : De Gruyter, [2022]Copyright date: ©1983Edition: Reprint 2021Description: 1 online resource (104 p.)Content type:
Media type:
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ISBN:
  • 9783112544235
  • 9783112544242
Subject(s): Other classification:
  • online - DeGruyter
Online resources: Available additional physical forms:
  • Issued also in print.
Contents:
Frontmatter -- Preface -- Table of Contents -- I. Introduction -- II. Structures -- 1. Non-delocalized (σ) -- 2. Delocalized (π) -- III. Preparations -- 1. From Alkyl Halides -- 2. From Alkanes by Proton Abstraction (3-2) -- 3. From Unsaturated Compounds -- 4. From Other Organometallics by Changing the Metal -- IV. Reactions of a Carbanions with Electrophiles -- 1. Substitution Reactions of Alkyl (sp3) Anions -- 2. Addition Reactions of Alkyl (sp3) Anions -- 3. Vinyl (sp2), Aryl (sp2), and Acetylenic (sp) Anions -- V. Reactions of π Carbanions with Electrophiles π -- 1. Hydrocarbon π Anions -- 2. Enolate Anions -- 3. Other O-Stabilized Monoanions -- 4. O-Stabilized Dianions -- 5. N-Stabilized Anions -- 6. S-Stabilized Anions -- VI. Eliminations -- 1. α-Eliminations -- 2. β-Eliminations -- 3. γ-Eliminations -- 4. δ-Eliminations -- 5. Cycloeliminations -- VII. Oxidations -- 1. Oxidations to Hydroperoxides, Alcohols, and Ketones -- 2. Oxidative Couplings -- 3. Dianion Oxidations -- Vm. Rearrangements -- 1. Intermolecular Rearrangements -- 2. Intramolecular Additions -- 3. Intramolecular Eliminations -- 4. Sigmatropic Carbanion Rearrangements -- 4. Sigmatropic Carbanion Rearrangements -- 6. Complex Intramolecular Rearrangements -- IX. Carbanion Equivalents -- X. Summary -- XI. References
Holdings
Item type Current library Call number URL Status Notes Barcode
eBook eBook Biblioteca "Angelicum" Pont. Univ. S.Tommaso d'Aquino Nuvola online online - DeGruyter (Browse shelf(Opens below)) Online access Not for loan (Accesso limitato) Accesso per gli utenti autorizzati / Access for authorized users (dgr)9783112544242

Frontmatter -- Preface -- Table of Contents -- I. Introduction -- II. Structures -- 1. Non-delocalized (σ) -- 2. Delocalized (π) -- III. Preparations -- 1. From Alkyl Halides -- 2. From Alkanes by Proton Abstraction (3-2) -- 3. From Unsaturated Compounds -- 4. From Other Organometallics by Changing the Metal -- IV. Reactions of a Carbanions with Electrophiles -- 1. Substitution Reactions of Alkyl (sp3) Anions -- 2. Addition Reactions of Alkyl (sp3) Anions -- 3. Vinyl (sp2), Aryl (sp2), and Acetylenic (sp) Anions -- V. Reactions of π Carbanions with Electrophiles π -- 1. Hydrocarbon π Anions -- 2. Enolate Anions -- 3. Other O-Stabilized Monoanions -- 4. O-Stabilized Dianions -- 5. N-Stabilized Anions -- 6. S-Stabilized Anions -- VI. Eliminations -- 1. α-Eliminations -- 2. β-Eliminations -- 3. γ-Eliminations -- 4. δ-Eliminations -- 5. Cycloeliminations -- VII. Oxidations -- 1. Oxidations to Hydroperoxides, Alcohols, and Ketones -- 2. Oxidative Couplings -- 3. Dianion Oxidations -- Vm. Rearrangements -- 1. Intermolecular Rearrangements -- 2. Intramolecular Additions -- 3. Intramolecular Eliminations -- 4. Sigmatropic Carbanion Rearrangements -- 4. Sigmatropic Carbanion Rearrangements -- 6. Complex Intramolecular Rearrangements -- IX. Carbanion Equivalents -- X. Summary -- XI. References

restricted access online access with authorization star

http://purl.org/coar/access_right/c_16ec

Issued also in print.

Mode of access: Internet via World Wide Web.

In English.

Description based on online resource; title from PDF title page (publisher's Web site, viewed 01. Dez 2022)