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Merck
  • Metal enolates of alpha-CF3 ketones: theoretical guideline, direct generation, and synthetic use.

Metal enolates of alpha-CF3 ketones: theoretical guideline, direct generation, and synthetic use.

Chemical record (New York, N.Y.) (2006-02-14)
Koichi Mikami, Yoshimitsu Itoh
ABSTRACT

The difficulty as well as the significance of the direct generation of metal enolates of alpha-CF(3) ketones cannot be easily understood by chemists unfamiliar with F. In sharp contrast to the sunny side of non-F, hydrocarbon chemistry, F chemistry has long been overshadowed. Metal enolates of carbonyl compounds are synthetically important in C-C bond-forming reactions. However, the metal enolates of fluorinated carbonyl compounds have been severely limited to alpha-F metal enolates. Alpha-CF(3) metal enolates have generally been recognized as unstable and difficult to prepare because of the facile beta-M-F elimination. However, we have developed a direct generation and synthetic application of alpha-CF(3) metal enolates. Therefore, the present results regarding the direct generation and synthetic use of metal enolates of alpha-CF(3) ketones might be recognized as a real breakthrough for the general use of metal enolates in F chemistry.

MATERIALS
Product Number
Brand
Product Description

Supelco
Diisopropylamine, analytical standard
Sigma-Aldrich
Diisopropylamine, puriss. p.a., ≥99.0% (GC)
Sigma-Aldrich
Diisopropylamine, SAJ first grade, ≥98.0%
Sigma-Aldrich
Diisopropylamine, ≥99.5%
Sigma-Aldrich
Lithium diisopropylamide solution, 2.0 M in THF/heptane/ethylbenzene
Sigma-Aldrich
Lithium diisopropylamide, 97%
Sigma-Aldrich
Diisopropylamine, purified by redistillation, 99.95%