SELECTIVE FORMATION OF KETONE, DIKETONE AND ALDEHYDE BY THE CO INSERTION INTO NICKEL–ALKYL BONDS OF DIALKYLNICKEL COMPLEXES. A NOVEL NICKEL-CATALYZED SYNTHESES OF KETONES AND TERTIARY ALCOHOLS FROM GRIGNARD REAGENTS, ARYL HALIDES, AND CARBON MONOXIDE-Reference-Cited by-同舟云学术

SELECTIVE FORMATION OF KETONE, DIKETONE AND ALDEHYDE BY THE CO INSERTION INTO NICKEL–ALKYL BONDS OF DIALKYLNICKEL COMPLEXES. A NOVEL NICKEL-CATALYZED SYNTHESES OF KETONES AND TERTIARY ALCOHOLS FROM GRIGNARD REAGENTS, ARYL HALIDES, AND CARBON MONOXIDE

Published:1976-11-05 Issue:11 Volume:5 Page:1217-1220
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Yamamoto Takakazu,Kohara Teiji,Yamamoto Akio

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference18 articles.

1. Carbon-carbon bond formation via oxidative addition to vinylrhodium(I) complexes. New stereospecific synthesis of trisubstituted olefins from disubstituted acetylenes

2. Disodium tetracarbonylferrate, a transition metal analog of a Grignard reagent

3. Formation of ethyl ketones through sequential insertion reactions of alkyl tetracarbonylferrates

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