Chemie nucleophiler Carbene, XVII Zur Kenntnis der anomalen α-Eliminierung Aldehyde aus 1.3-Diphenyl-2-alkoxy-imidazolidinen und Grignard-Verbindungen-Reference-Cited by-同舟云学术

Chemie nucleophiler Carbene, XVII Zur Kenntnis der anomalen α-Eliminierung Aldehyde aus 1.3-Diphenyl-2-alkoxy-imidazolidinen und Grignard-Verbindungen

Published:1969-12-12 Issue:1 Volume:729 Page:27-32
ISSN:0075-4617
Container-title:Justus Liebigs Annalen der Chemie
language:de
Short-container-title:Justus Liebigs Ann. Chem.

Author:

Lachmann Burkhard,Wanzlick Hans-Werner

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry,General Medicine

Reference33 articles.

1. Chemie nucleophiler Carbene, XVI. 2‐Thio‐coffein und 5‐Oxo‐7‐methylimino‐1.4‐dimethyl‐1.4.5.7‐tetrahydro‐imidazo[4.5‐ d ][1.3]thiazin

2. Zwischenstufen der α-Eliminierung

3. Intermediates ofα-Eliminations

4. Carbon Dichloride as an Intermediate in the Basic Hydrolysis of Chloroform. A Mechanism for Substitution Reactions at a Saturated Carbon Atom1

5. Methylene Derivatives as Intermediates in Polar Reactions. IX. The Concerted Mechanism for α-Eliminations of Haloforms1

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